| geneid | 4293 |
|---|---|
| ensemblid | ENSG00000006432.16 |
| hgncid | 6861 |
| symbol | MAP3K9 |
| name | mitogen-activated protein kinase kinase kinase 9 |
| refseq_nuc | NM_001284230.2 |
| refseq_prot | NP_001271159.1 |
| ensembl_nuc | ENST00000554752.7 |
| ensembl_prot | ENSP00000451612.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 70722526 |
| end | 70809513 |
| strand | - |
| ver | v1.2 |
| region | chr14:70722526-70809513 |
| region5000 | chr14:70717526-70814513 |
| regionname0 | MAP3K9_chr14_70722526_70809513 |
| regionname5000 | MAP3K9_chr14_70717526_70814513 |
| 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 | 1104 | 361 | 78 | 64 | 173 | 13 | 31 | 133 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0002 | 0/0 | 1104 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0003 | 0/0 | 1104 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0004 | 0/0 | 1104 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0005 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0006 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0007 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0008 | 0/0 | 1104 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0009 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0010 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0011 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0012 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| 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 | 3315 | 262 | 49 | 46 | 134 | 8 | 23 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0002 | 0/0 | 3315 | 70 | 11 | 15 | 37 | 1 | 6 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0003 | 0/0 | 3315 | 10 | 4 | 3 | 0 | 1 | 2 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0004 | 0/0 | 3315 | 5 | 5 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0005 | 0/0 | 3315 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0006 | 0/0 | 3315 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0007 | 0/0 | 3315 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0008 | 0/0 | 3315 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0009 | 0/0 | 3315 | 2 | 0 | 0 | 0 | 2 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0010 | 0/0 | 3315 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0011 | 0/0 | 3315 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0012 | 0/0 | 3315 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0013 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0014 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0015 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0016 | 0/0 | 3315 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0017 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0018 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0019 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0020 | 0/0 | 3315 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0021 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| c0022 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 8185 | 40 | 3 | 16 | 15 | 3 | 3 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0002 | 0/0 | 8196 | 30 | 4 | 0 | 25 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0003 | 0/1 | 8202 | 30 | 1 | 6 | 13 | 2 | 7 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0004 | 1/0 | 8197 | 28 | 1 | 3 | 20 | 0 | 3 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0005 | 0/0 | 8202 | 25 | 2 | 2 | 21 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0006 | 0/0 | 8197 | 18 | 0 | 7 | 8 | 2 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0007 | 0/0 | 8183 | 12 | 9 | 1 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0008 | 0/0 | 8186 | 10 | 1 | 1 | 6 | 0 | 2 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0009 | 0/0 | 8204 | 10 | 0 | 7 | 0 | 1 | 2 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0010 | 0/0 | 8197 | 9 | 0 | 0 | 9 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0011 | 0/0 | 8202 | 6 | 0 | 3 | 0 | 1 | 2 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0012 | 0/0 | 8182 | 5 | 5 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0013 | 0/0 | 8196 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0014 | 0/0 | 8202 | 4 | 2 | 0 | 1 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0015 | 0/0 | 8202 | 4 | 3 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0016 | 0/0 | 8185 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0017 | 0/0 | 8199 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0018 | 0/0 | 8203 | 4 | 0 | 2 | 1 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0019 | 0/0 | 8197 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0020 | 0/0 | 8185 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0021 | 0/0 | 8196 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0022 | 0/0 | 8185 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0023 | 0/0 | 8184 | 3 | 1 | 1 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0024 | 0/0 | 8198 | 3 | 0 | 1 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0025 | 0/0 | 8198 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0026 | 0/0 | 8202 | 3 | 0 | 2 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0027 | 0/0 | 8203 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0028 | 0/0 | 8184 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0029 | 0/0 | 8184 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0030 | 0/0 | 8196 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0031 | 0/0 | 8203 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0032 | 0/0 | 8185 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0033 | 0/0 | 8200 | 2 | 0 | 0 | 0 | 2 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0034 | 0/0 | 8202 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0035 | 0/0 | 8202 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0036 | 0/0 | 8203 | 2 | 1 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0037 | 0/0 | 8201 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0038 | 0/0 | 8186 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0039 | 0/0 | 8197 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0040 | 0/0 | 8197 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0041 | 0/0 | 8203 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0042 | 0/0 | 8186 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0043 | 0/0 | 8186 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0044 | 0/0 | 8198 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0045 | 0/0 | 8197 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0046 | 0/0 | 8197 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0047 | 0/0 | 8196 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0048 | 0/0 | 8195 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0049 | 0/0 | 8185 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0050 | 0/0 | 8185 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0051 | 0/0 | 8202 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0052 | 0/0 | 8205 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0053 | 0/0 | 8203 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0054 | 0/0 | 8200 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0055 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0056 | 0/0 | 8187 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0057 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0058 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0059 | 0/0 | 8186 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0060 | 0/0 | 8185 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0061 | 0/0 | 8185 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0062 | 0/0 | 8186 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0063 | 0/0 | 8187 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0064 | 0/0 | 8197 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0065 | 0/0 | 8197 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0066 | 0/0 | 8197 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0067 | 0/0 | 8183 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0068 | 0/0 | 8185 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0069 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0070 | 0/0 | 8186 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0071 | 0/0 | 8198 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0072 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0073 | 0/0 | 8204 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0074 | 0/0 | 8200 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0075 | 0/0 | 8200 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0076 | 0/0 | 8200 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0077 | 0/0 | 8199 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0078 | 0/0 | 8198 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0079 | 0/0 | 8204 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0080 | 0/0 | 8203 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0081 | 0/0 | 8202 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0082 | 0/0 | 8198 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0083 | 0/0 | 8198 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0084 | 0/0 | 8203 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0085 | 0/0 | 8197 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0086 | 0/0 | 8198 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0087 | 0/0 | 8204 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0088 | 0/0 | 8203 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0089 | 0/0 | 8206 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0090 | 0/0 | 8205 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0091 | 0/0 | 8205 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0092 | 0/0 | 8203 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0093 | 0/0 | 8202 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0094 | 0/0 | 8198 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0095 | 0/0 | 8199 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0096 | 0/0 | 8198 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0097 | 0/0 | 8198 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0098 | 0/0 | 8197 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0099 | 0/0 | 8202 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0100 | 0/0 | 8197 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0101 | 0/0 | 8204 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0102 | 0/0 | 8203 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0103 | 0/0 | 8203 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0104 | 0/0 | 8204 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0105 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0106 | 0/0 | 8204 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0107 | 0/0 | 8203 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0108 | 0/0 | 8197 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0109 | 0/0 | 8197 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0110 | 0/0 | 8197 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0111 | 0/0 | 8182 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0112 | 0/0 | 8182 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0113 | 0/0 | 8183 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0114 | 0/0 | 8197 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| t0115 | 0/0 | 8200 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| 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 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0347 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| 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 | 3315 | 262 | 49 | 46 | 134 | 8 | 23 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002 | 0/0 | 3315 | 70 | 11 | 15 | 37 | 1 | 6 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0003 | 0/0 | 3315 | 10 | 4 | 3 | 0 | 1 | 2 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0004 | 0/0 | 3315 | 5 | 5 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0005 | 0/0 | 3315 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0006 | 0/0 | 3315 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0009 | 0/0 | 3315 | 2 | 0 | 0 | 0 | 2 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0011 | 0/0 | 3315 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0013 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0018 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0021 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0002c0008 | 0/0 | 3315 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0003c0007 | 0/0 | 3315 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0004c0020 | 0/0 | 3315 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0005c0012 | 0/0 | 3315 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0006c0014 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0007c0015 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0008c0016 | 0/0 | 3315 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0009c0017 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0010c0019 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0011c0010 | 0/0 | 3315 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0012c0022 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 11510 | 30 | 4 | 0 | 25 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0003 | 0/1 | 11516 | 26 | 1 | 5 | 11 | 2 | 6 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0004 | 1/0 | 11511 | 27 | 1 | 3 | 19 | 0 | 3 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0005 | 0/0 | 11516 | 22 | 0 | 2 | 20 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0006 | 0/0 | 11511 | 18 | 0 | 7 | 8 | 2 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0007 | 0/0 | 11497 | 10 | 7 | 1 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0009 | 0/0 | 11518 | 10 | 0 | 7 | 0 | 1 | 2 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0010 | 0/0 | 11511 | 9 | 0 | 0 | 9 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0011 | 0/0 | 11516 | 6 | 0 | 3 | 0 | 1 | 2 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0012 | 0/0 | 11496 | 5 | 5 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0013 | 0/0 | 11510 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0014 | 0/0 | 11516 | 4 | 2 | 0 | 1 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0015 | 0/0 | 11516 | 3 | 2 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0018 | 0/0 | 11517 | 4 | 0 | 2 | 1 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0019 | 0/0 | 11511 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0021 | 0/0 | 11510 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0024 | 0/0 | 11512 | 3 | 0 | 1 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0025 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0026 | 0/0 | 11516 | 3 | 0 | 2 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0027 | 0/0 | 11517 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0028 | 0/0 | 11498 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0030 | 0/0 | 11510 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0031 | 0/0 | 11517 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0034 | 0/0 | 11516 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0035 | 0/0 | 11516 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0036 | 0/0 | 11517 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0037 | 0/0 | 11515 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0039 | 0/0 | 11511 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0040 | 0/0 | 11511 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0041 | 0/0 | 11517 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0044 | 0/0 | 11512 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0045 | 0/0 | 11511 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0046 | 0/0 | 11511 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0047 | 0/0 | 11510 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0048 | 0/0 | 11509 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0052 | 0/0 | 11519 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0053 | 0/0 | 11517 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0054 | 0/0 | 11514 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0055 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0057 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0058 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0065 | 0/0 | 11511 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0066 | 0/0 | 11511 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0069 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0072 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0073 | 0/0 | 11518 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0074 | 0/0 | 11514 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0075 | 0/0 | 11514 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0076 | 0/0 | 11514 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0077 | 0/0 | 11513 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0078 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0079 | 0/0 | 11518 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0080 | 0/0 | 11517 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0081 | 0/0 | 11516 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0082 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0084 | 0/0 | 11517 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0085 | 0/0 | 11511 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0086 | 0/0 | 11512 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0087 | 0/0 | 11518 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0088 | 0/0 | 11517 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0089 | 0/0 | 11520 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0090 | 0/0 | 11519 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0091 | 0/0 | 11519 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0092 | 0/0 | 11517 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0093 | 0/0 | 11516 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0095 | 0/0 | 11513 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0097 | 0/0 | 11512 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0099 | 0/0 | 11516 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0100 | 0/0 | 11511 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0101 | 0/0 | 11518 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0102 | 0/0 | 11517 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0103 | 0/0 | 11517 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0104 | 0/0 | 11518 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0105 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0106 | 0/0 | 11518 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0107 | 0/0 | 11517 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0110 | 0/0 | 11511 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0111 | 0/0 | 11496 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0112 | 0/0 | 11496 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0113 | 0/0 | 11497 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0114 | 0/0 | 11511 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0001t0115 | 0/0 | 11514 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0001 | 0/0 | 11499 | 34 | 2 | 13 | 15 | 1 | 3 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0008 | 0/0 | 11500 | 8 | 0 | 1 | 6 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0016 | 0/0 | 11499 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0020 | 0/0 | 11499 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0022 | 0/0 | 11499 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0023 | 0/0 | 11498 | 3 | 1 | 1 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0029 | 0/0 | 11498 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0032 | 0/0 | 11499 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0038 | 0/0 | 11500 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0042 | 0/0 | 11500 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0043 | 0/0 | 11500 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0050 | 0/0 | 11499 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0059 | 0/0 | 11500 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0060 | 0/0 | 11499 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0061 | 0/0 | 11499 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0062 | 0/0 | 11500 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0063 | 0/0 | 11501 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0068 | 0/0 | 11499 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0002t0070 | 0/0 | 11500 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0003t0001 | 0/0 | 11499 | 5 | 1 | 3 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0003t0008 | 0/0 | 11500 | 2 | 1 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0003t0049 | 0/0 | 11499 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0003t0056 | 0/0 | 11501 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0003t0109 | 0/0 | 11511 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0004t0007 | 0/0 | 11497 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0004t0028 | 0/0 | 11498 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0004t0067 | 0/0 | 11497 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0005t0005 | 0/0 | 11516 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0005t0036 | 0/0 | 11517 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0005t0098 | 0/0 | 11511 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0006t0017 | 0/0 | 11513 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0009t0033 | 0/0 | 11514 | 2 | 0 | 0 | 0 | 2 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0011t0051 | 0/0 | 11516 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0013t0005 | 0/0 | 11516 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0018t0083 | 0/0 | 11512 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0001c0021t0071 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0002c0008t0003 | 0/0 | 11516 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0003c0007t0064 | 0/0 | 11511 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0003c0007t0096 | 0/0 | 11512 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0004c0020t0108 | 0/0 | 11511 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0005c0012t0001 | 0/0 | 11499 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0006c0014t0015 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0007c0015t0004 | 0/0 | 11511 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0008c0016t0003 | 0/0 | 11516 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0009c0017t0025 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0010c0019t0025 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0011c0010t0003 | 0/0 | 11516 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| a0012c0022t0094 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | copy fasta | chr14 | 70717526 | 70814513 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0347 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0007g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0007g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0007g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0007g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0007g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0009g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0009g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0009g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0009g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0009g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0009g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0009g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0009g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0009g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0009g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0010g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0010g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0010g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0010g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0010g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0010g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0010g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0010g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0011g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0011g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0011g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0011g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0012g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0012g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0012g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0012g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0013g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0013g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0013g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0013g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0014g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0014g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0014g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0014g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0015g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0015g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0015g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0018g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0018g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0018g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0018g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0019g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0019g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0019g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0019g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0021g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0021g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0021g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0024g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0024g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0024g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0025g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0026g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0026g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0026g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0027g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0027g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0027g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0028g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0030g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0030g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0031g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0031g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0034g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0034g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0035g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0035g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0036g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0037g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0037g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0039g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0040g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0041g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0044g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0045g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0046g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0047g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0048g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0052g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0053g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0054g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0055g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0057g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0058g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0065g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0066g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0069g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0072g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0073g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0074g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0075g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0076g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0077g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0078g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0079g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0080g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0081g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0082g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0084g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0085g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0086g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0087g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0088g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0089g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0090g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0091g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0092g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0093g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0095g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0097g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0099g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0100g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0101g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0102g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0103g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0104g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0105g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0106g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0107g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0110g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0111g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0112g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0113g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0114g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0001t0115g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0008g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0008g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0008g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0008g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0008g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0008g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0008g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0016g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0016g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0016g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0020g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0020g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0022g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0022g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0022g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0023g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0023g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0023g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0029g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0032g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0032g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0038g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0042g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0043g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0050g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0059g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0060g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0061g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0062g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0063g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0068g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0002t0070g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0003t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0003t0008g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0003t0049g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0003t0056g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0003t0109g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0004t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0004t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0004t0028g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0004t0028g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0004t0067g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0005t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0005t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0005t0036g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0005t0098g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0006t0017g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0006t0017g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0006t0017g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0006t0017g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0009t0033g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0009t0033g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0011t0051g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0013t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0018t0083g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0001c0021t0071g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0002c0008t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0002c0008t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0003c0007t0064g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0003c0007t0096g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0004c0020t0108g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0005c0012t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0006c0014t0015g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0007c0015t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0008c0016t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0009c0017t0025g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0010c0019t0025g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0011c0010t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| a0012c0022t0094g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0094 | EUR | GBR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00099 | hp2 | a0001 | c0009 | t0033 | g0124 | EUR | GBR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00140 | hp1 | a0001 | c0001 | t0104 | g0286 | EUR | GBR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0214 | EUR | GBR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0148 | EUR | FIN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00280 | hp2 | a0001 | c0001 | t0011 | g0293 | EUR | FIN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0086 | EUR | FIN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00323 | hp2 | a0001 | c0001 | t0009 | g0304 | EUR | FIN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00408 | hp1 | a0001 | c0001 | t0021 | g0122 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00438 | hp1 | a0001 | c0002 | t0008 | g0174 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00438 | hp2 | a0001 | c0001 | t0035 | g0230 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00597 | hp1 | a0001 | c0001 | t0039 | g0014 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00609 | hp1 | a0001 | c0018 | t0083 | g0228 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0310 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00621 | hp1 | a0001 | c0002 | t0008 | g0172 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0336 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00639 | hp2 | a0001 | c0001 | t0009 | g0290 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00642 | hp2 | a0001 | c0001 | t0107 | g0291 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0264 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0350 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0285 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00735 | hp1 | a0001 | c0001 | t0101 | g0275 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00735 | hp2 | a0001 | c0001 | t0018 | g0204 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00741 | hp1 | a0001 | c0001 | t0009 | g0292 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0077 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0345 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01070 | hp1 | a0001 | c0002 | t0023 | g0107 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0269 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0344 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0298 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01074 | hp1 | a0001 | c0001 | t0106 | g0261 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01074 | hp2 | a0001 | c0001 | t0011 | g0009 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01081 | hp1 | a0008 | c0016 | t0003 | g0205 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01081 | hp2 | a0001 | c0001 | t0041 | g0018 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01099 | hp1 | a0001 | c0001 | t0011 | g0009 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01106 | hp2 | a0001 | c0001 | t0112 | g0325 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01109 | hp1 | a0004 | c0020 | t0108 | g0334 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01109 | hp2 | a0003 | c0007 | t0064 | g0150 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0069 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0070 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0109 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01192 | hp1 | a0001 | c0001 | t0076 | g0187 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0346 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0110 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0113 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0163 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01256 | hp2 | a0001 | c0001 | t0026 | g0223 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01257 | hp2 | a0001 | c0001 | t0009 | g0263 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01258 | hp2 | a0001 | c0001 | t0026 | g0201 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01346 | hp1 | a0001 | c0001 | t0079 | g0192 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01346 | hp2 | a0001 | c0001 | t0099 | g0284 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01358 | hp1 | a0001 | c0001 | t0009 | g0273 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0108 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01361 | hp1 | a0001 | c0001 | t0080 | g0221 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01433 | hp1 | a0001 | c0001 | t0052 | g0173 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01433 | hp2 | a0001 | c0001 | t0015 | g0131 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01496 | hp1 | a0001 | c0001 | t0018 | g0193 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01496 | hp2 | a0003 | c0007 | t0096 | g0257 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0147 | EUR | IBS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0226 | EUR | IBS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01884 | hp1 | a0001 | c0004 | t0007 | g0276 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01884 | hp2 | a0001 | c0006 | t0017 | g0165 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01891 | hp1 | a0001 | c0001 | t0012 | g0031 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01891 | hp2 | a0001 | c0001 | t0055 | g0085 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01943 | hp1 | a0001 | c0002 | t0008 | g0120 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01943 | hp2 | a0001 | c0001 | t0009 | g0281 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01952 | hp1 | a0001 | c0001 | t0090 | g0249 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01952 | hp2 | a0001 | c0001 | t0024 | g0142 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01981 | hp1 | a0001 | c0001 | t0006 | g0151 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0215 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0156 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0153 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02004 | hp2 | a0001 | c0001 | t0093 | g0252 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02015 | hp2 | a0001 | c0002 | t0016 | g0005 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02040 | hp1 | a0001 | c0002 | t0032 | g0078 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0341 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02055 | hp1 | a0001 | c0001 | t0087 | g0250 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02055 | hp2 | a0012 | c0022 | t0094 | g0259 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02056 | hp1 | a0001 | c0001 | t0027 | g0245 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0299 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02074 | hp1 | a0001 | c0001 | t0088 | g0254 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0305 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02083 | hp1 | a0001 | c0001 | t0035 | g0231 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02083 | hp2 | a0001 | c0002 | t0032 | g0178 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02132 | hp1 | a0001 | c0002 | t0016 | g0091 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0302 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02135 | hp2 | a0001 | c0001 | t0097 | g0253 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02145 | hp1 | a0001 | c0001 | t0015 | g0137 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02145 | hp2 | a0001 | c0001 | t0077 | g0183 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | CDX | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02155 | hp2 | a0001 | c0002 | t0068 | g0101 | EAS | CDX | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02257 | hp1 | a0001 | c0001 | t0082 | g0227 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0083 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02258 | hp1 | a0001 | c0001 | t0012 | g0020 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02258 | hp2 | a0001 | c0001 | t0014 | g0127 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02273 | hp2 | a0001 | c0001 | t0006 | g0160 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02280 | hp1 | a0001 | c0001 | t0115 | g0319 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02293 | hp1 | a0001 | c0001 | t0009 | g0288 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0159 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0152 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02300 | hp2 | a0001 | c0001 | t0009 | g0355 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02451 | hp1 | a0001 | c0001 | t0075 | g0189 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02451 | hp2 | a0001 | c0001 | t0015 | g0133 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02523 | hp1 | a0001 | c0001 | t0006 | g0145 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0315 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02572 | hp1 | a0001 | c0005 | t0005 | g0323 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02572 | hp2 | a0009 | c0017 | t0025 | g0180 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02602 | hp2 | a0001 | c0002 | t0063 | g0115 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02615 | hp1 | a0001 | c0001 | t0025 | g0025 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02615 | hp2 | a0001 | c0002 | t0050 | g0068 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02622 | hp1 | a0001 | c0001 | t0073 | g0190 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02622 | hp2 | a0001 | c0002 | t0029 | g0006 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02630 | hp2 | a0001 | c0001 | t0034 | g0130 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02647 | hp1 | a0006 | c0014 | t0015 | g0135 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02647 | hp2 | a0001 | c0001 | t0028 | g0244 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0100 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0213 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02698 | hp1 | a0011 | c0010 | t0003 | g0209 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02698 | hp2 | a0001 | c0001 | t0009 | g0289 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02717 | hp1 | a0001 | c0001 | t0113 | g0356 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02717 | hp2 | a0001 | c0006 | t0017 | g0139 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02723 | hp1 | a0001 | c0002 | t0022 | g0023 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02723 | hp2 | a0001 | c0001 | t0012 | g0032 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02738 | hp1 | a0001 | c0001 | t0018 | g0224 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02738 | hp2 | a0001 | c0002 | t0008 | g0114 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02809 | hp1 | a0001 | c0006 | t0017 | g0140 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0030 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0283 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02895 | hp2 | a0001 | c0003 | t0109 | g0327 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0266 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02897 | hp2 | a0001 | c0001 | t0034 | g0129 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0326 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02922 | hp2 | a0001 | c0001 | t0058 | g0134 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0279 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02965 | hp2 | a0001 | c0002 | t0023 | g0073 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02970 | hp2 | a0001 | c0002 | t0059 | g0024 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0222 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0330 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03041 | hp1 | a0001 | c0001 | t0111 | g0280 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03041 | hp2 | a0001 | c0004 | t0067 | g0033 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03098 | hp1 | a0001 | c0003 | t0056 | g0067 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03098 | hp2 | a0001 | c0001 | t0031 | g0136 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03130 | hp1 | a0001 | c0001 | t0069 | g0128 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03130 | hp2 | a0001 | c0005 | t0036 | g0322 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03139 | hp1 | a0001 | c0002 | t0060 | g0021 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0274 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03195 | hp1 | a0001 | c0005 | t0005 | g0324 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03195 | hp2 | a0001 | c0004 | t0028 | g0247 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03209 | hp1 | a0001 | c0001 | t0030 | g0167 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03209 | hp2 | a0001 | c0001 | t0103 | g0262 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03453 | hp1 | a0001 | c0005 | t0098 | g0320 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03453 | hp2 | a0001 | c0001 | t0012 | g0034 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03486 | hp1 | a0001 | c0001 | t0105 | g0260 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03486 | hp2 | a0010 | c0019 | t0025 | g0181 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03490 | hp1 | a0001 | c0001 | t0011 | g0010 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03490 | hp2 | a0001 | c0001 | t0065 | g0149 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03492 | hp1 | a0001 | c0001 | t0011 | g0010 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03492 | hp2 | a0001 | c0001 | t0026 | g0220 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03516 | hp1 | a0001 | c0002 | t0022 | g0022 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03516 | hp2 | a0001 | c0002 | t0022 | g0084 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03540 | hp1 | a0001 | c0001 | t0054 | g0125 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03540 | hp2 | a0001 | c0003 | t0008 | g0170 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03579 | hp1 | a0001 | c0001 | t0030 | g0168 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03579 | hp2 | a0001 | c0001 | t0014 | g0126 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03654 | hp1 | a0001 | c0003 | t0008 | g0179 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03654 | hp2 | a0001 | c0001 | t0014 | g0186 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03669 | hp1 | a0001 | c0003 | t0049 | g0087 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0342 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03710 | hp2 | a0001 | c0001 | t0091 | g0248 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03831 | hp1 | a0001 | c0001 | t0095 | g0258 | SAS | BEB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03831 | hp2 | a0001 | c0001 | t0081 | g0210 | SAS | BEB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03834 | hp1 | a0001 | c0001 | t0100 | g0340 | SAS | BEB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03834 | hp2 | a0001 | c0001 | t0009 | g0265 | SAS | BEB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG04115 | hp1 | a0001 | c0001 | t0110 | g0332 | SAS | STU | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | STU | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG04184 | hp1 | a0001 | c0001 | t0006 | g0166 | SAS | BEB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0351 | SAS | BEB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0217 | SAS | STU | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG04199 | hp2 | a0001 | c0002 | t0043 | g0017 | SAS | STU | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | STU | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0194 | SAS | STU | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | YRI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18522 | hp2 | a0001 | c0002 | t0029 | g0006 | AFR | YRI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0306 | EAS | CHB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | CHB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18747 | hp1 | a0001 | c0001 | t0102 | g0267 | EAS | CHB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0155 | EAS | CHB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18906 | hp1 | a0001 | c0004 | t0028 | g0243 | AFR | YRI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18906 | hp2 | a0001 | c0001 | t0078 | g0182 | AFR | YRI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18939 | hp1 | a0001 | c0001 | t0021 | g0051 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18941 | hp1 | a0001 | c0001 | t0019 | g0360 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18943 | hp1 | a0001 | c0002 | t0061 | g0095 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0307 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18948 | hp1 | a0001 | c0001 | t0048 | g0062 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18948 | hp2 | a0001 | c0001 | t0005 | g0317 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18949 | hp1 | a0001 | c0001 | t0046 | g0046 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18949 | hp2 | a0001 | c0001 | t0086 | g0235 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18950 | hp1 | a0001 | c0001 | t0013 | g0044 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18950 | hp2 | a0001 | c0001 | t0053 | g0090 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18954 | hp1 | a0001 | c0002 | t0023 | g0074 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18956 | hp1 | a0001 | c0001 | t0040 | g0015 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18957 | hp2 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18960 | hp2 | a0001 | c0001 | t0019 | g0359 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0313 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18962 | hp2 | a0001 | c0001 | t0006 | g0157 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0339 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18964 | hp1 | a0001 | c0001 | t0010 | g0240 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18964 | hp2 | a0002 | c0008 | t0003 | g0216 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18967 | hp1 | a0001 | c0002 | t0020 | g0013 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18967 | hp2 | a0001 | c0001 | t0027 | g0255 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18968 | hp2 | a0001 | c0001 | t0010 | g0239 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0312 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18972 | hp1 | a0001 | c0002 | t0038 | g0012 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0296 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0301 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0333 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18975 | hp2 | a0001 | c0001 | t0092 | g0251 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18978 | hp1 | a0001 | c0001 | t0010 | g0241 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18978 | hp2 | a0001 | c0001 | t0013 | g0042 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18979 | hp1 | a0001 | c0013 | t0005 | g0282 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18980 | hp1 | a0001 | c0001 | t0021 | g0121 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18980 | hp2 | a0001 | c0002 | t0016 | g0005 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18982 | hp2 | a0001 | c0002 | t0070 | g0092 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18983 | hp1 | a0001 | c0001 | t0007 | g0270 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18984 | hp2 | a0001 | c0001 | t0066 | g0146 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0343 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18989 | hp2 | a0001 | c0001 | t0007 | g0309 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18990 | hp1 | a0001 | c0001 | t0018 | g0200 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18990 | hp2 | a0001 | c0001 | t0010 | g0237 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0335 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18991 | hp2 | a0001 | c0001 | t0084 | g0229 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18992 | hp2 | a0002 | c0008 | t0003 | g0218 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18994 | hp1 | a0001 | c0001 | t0036 | g0294 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0349 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18995 | hp1 | a0001 | c0001 | t0014 | g0185 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18995 | hp2 | a0001 | c0001 | t0013 | g0035 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18998 | hp2 | a0001 | c0001 | t0019 | g0357 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18999 | hp1 | a0001 | c0001 | t0013 | g0043 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0337 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19000 | hp1 | a0001 | c0001 | t0089 | g0256 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19000 | hp2 | a0001 | c0002 | t0062 | g0079 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19001 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19001 | hp2 | a0001 | c0001 | t0005 | g0316 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19003 | hp1 | a0001 | c0002 | t0016 | g0089 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19003 | hp2 | a0001 | c0001 | t0037 | g0268 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19004 | hp1 | a0001 | c0002 | t0020 | g0003 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19004 | hp2 | a0001 | c0001 | t0010 | g0233 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0331 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0353 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0314 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19010 | hp1 | a0007 | c0015 | t0004 | g0271 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19011 | hp2 | a0001 | c0001 | t0010 | g0236 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19012 | hp1 | a0001 | c0001 | t0019 | g0358 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19012 | hp2 | a0001 | c0001 | t0027 | g0246 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19030 | hp1 | a0001 | c0021 | t0071 | g0143 | AFR | LWK | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19030 | hp2 | a0001 | c0004 | t0007 | g0277 | AFR | LWK | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0295 | AFR | LWK | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19043 | hp2 | a0001 | c0006 | t0017 | g0141 | AFR | LWK | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0297 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19056 | hp2 | a0001 | c0002 | t0042 | g0016 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19057 | hp2 | a0001 | c0001 | t0037 | g0311 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19058 | hp2 | a0001 | c0002 | t0008 | g0118 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19060 | hp1 | a0001 | c0001 | t0045 | g0045 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19062 | hp1 | a0001 | c0001 | t0047 | g0056 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19062 | hp2 | a0001 | c0001 | t0006 | g0161 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19076 | hp1 | a0001 | c0001 | t0085 | g0242 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19076 | hp2 | a0001 | c0001 | t0024 | g0169 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19078 | hp1 | a0001 | c0001 | t0044 | g0019 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0354 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19082 | hp1 | a0001 | c0001 | t0010 | g0234 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19084 | hp2 | a0001 | c0001 | t0010 | g0238 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0352 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19086 | hp1 | a0001 | c0002 | t0008 | g0171 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19086 | hp2 | a0001 | c0001 | t0024 | g0162 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19087 | hp1 | a0001 | c0002 | t0008 | g0076 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19087 | hp2 | a0001 | c0001 | t0010 | g0232 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19088 | hp2 | a0001 | c0001 | t0006 | g0158 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19090 | hp1 | a0001 | c0001 | t0006 | g0164 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19090 | hp2 | a0001 | c0002 | t0008 | g0080 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0303 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA19091 | hp2 | a0001 | c0002 | t0020 | g0003 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ASW | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA20129 | hp2 | a0001 | c0001 | t0074 | g0188 | AFR | ASW | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA20752 | hp1 | a0001 | c0011 | t0051 | g0184 | EUR | TSI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0026 | EUR | TSI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA20805 | hp1 | a0005 | c0012 | t0001 | g0112 | EUR | TSI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA20805 | hp2 | a0001 | c0009 | t0033 | g0123 | EUR | TSI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01123 | hp1 | a0001 | c0001 | t0011 | g0308 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02486 | hp1 | a0001 | c0001 | t0072 | g0191 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG02486 | hp2 | a0001 | c0001 | t0031 | g0138 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0318 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | USA | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA20300 | hp2 | a0001 | c0001 | t0114 | g0321 | AFR | USA | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA21309 | hp1 | a0001 | c0001 | t0057 | g0132 | AFR | LWK | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0348 | AFR | LWK | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0225 | REF | REF | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0347 | REF | REF | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:70730667
|
C | A | 1 | a0010 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.3028G>T | p.Val1010Leu | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3370/11511 | 3028/3315 | 1010/1104 | chr14 | 70730667 | ||
| chr14:70732700
|
C | T | 1 | a0009 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.2669G>A | p.Arg890Gln | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 3011/11511 | 2669/3315 | 890/1104 | chr14 | 70732700 | ||
| chr14:70732718
|
C | T | 1 | a0008 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.2651G>A | p.Arg884Gln | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2993/11511 | 2651/3315 | 884/1104 | chr14 | 70732718 | ||
| chr14:70732740
|
G | A | 1 | a0003 | 2 | HG01109.hp2 HG01496.hp2 |
missense_variant | MODERATE | c.2629C>T | p.His877Tyr | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2971/11511 | 2629/3315 | 877/1104 | chr14 | 70732740 | ||
| chr14:70733094
|
C | T | 1 | a0007 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.2275G>A | p.Val759Ile | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2617/11511 | 2275/3315 | 759/1104 | chr14 | 70733094 | ||
| chr14:70733198
|
A | C | 1 | a0006 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.2171T>G | p.Val724Gly | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2513/11511 | 2171/3315 | 724/1104 | chr14 | 70733198 | ||
| chr14:70733255
|
C | T | 1 | a0005 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.2114G>A | p.Arg705His | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2456/11511 | 2114/3315 | 705/1104 | chr14 | 70733255 | ||
| chr14:70733304
|
G | A | 1 | a0002 | 2 | NA18964.hp2 NA18992.hp2 |
missense_variant | MODERATE | c.2065C>T | p.Arg689Cys | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2407/11511 | 2065/3315 | 689/1104 | chr14 | 70733304 | ||
| chr14:70734475
|
T | C | 1 | a0004 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1937A>G | p.Tyr646Cys | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/12 | 2279/11511 | 1937/3315 | 646/1104 | chr14 | 70734475 | ||
| chr14:70761150
|
G | T | 1 | a0011 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.853C>A | p.Leu285Met | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/12 | 1195/11511 | 853/3315 | 285/1104 | chr14 | 70761150 | ||
| chr14:70809047
|
G | C | 1 | a0012 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.125C>G | p.Ala42Gly | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 467/11511 | 125/3315 | 42/1104 | chr14 | 70809047 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:70730455
|
G | A | 1 | a0001c0005 | 4 | HG02572.hp1 HG03130.hp2 HG03195.hp1 others(1): Show |
synonymous_variant | LOW | c.3240C>T | p.Thr1080Thr | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3582/11511 | 3240/3315 | 1080/1104 | chr14 | 70730455 | ||
| chr14:70730494
|
G | A | 1 | a0001c0021 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.3201C>T | p.Leu1067Leu | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3543/11511 | 3201/3315 | 1067/1104 | chr14 | 70730494 | ||
| chr14:70730533
|
C | T | 1 | a0001c0018 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.3162G>A | p.Pro1054Pro | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3504/11511 | 3162/3315 | 1054/1104 | chr14 | 70730533 | ||
| chr14:70732735
|
G | A | 4 | a0001c0002a0001c0003a0005c0012others(1): Show | 82 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
synonymous_variant | LOW | c.2634C>T | p.Asn878Asn | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2976/11511 | 2634/3315 | 878/1104 | chr14 | 70732735 | ||
| chr14:70733185
|
C | A | 1 | a0001c0004 | 5 | HG01884.hp1 HG03041.hp2 HG03195.hp2 others(2): Show |
synonymous_variant | LOW | c.2184G>T | p.Thr728Thr | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2526/11511 | 2184/3315 | 728/1104 | chr14 | 70733185 | ||
| chr14:70734429
|
C | T | 1 | a0001c0013 | 1 | NA18979.hp1 | synonymous_variant | LOW | c.1983G>A | p.Arg661Arg | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/12 | 2325/11511 | 1983/3315 | 661/1104 | chr14 | 70734429 | ||
| chr14:70734462
|
C | G | 1 | a0004c0020 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.1950G>C | p.Ser650Ser | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/12 | 2292/11511 | 1950/3315 | 650/1104 | chr14 | 70734462 | ||
| chr14:70734489
|
G | A | 2 | a0001c0009a0001c0011 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
synonymous_variant | LOW | c.1923C>T | p.Ser641Ser | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/12 | 2265/11511 | 1923/3315 | 641/1104 | chr14 | 70734489 | ||
| chr14:70735975
|
T | C | 2 | a0001c0006a0001c0021 | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
synonymous_variant | LOW | c.1899A>G | p.Pro633Pro | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/12 | 2241/11511 | 1899/3315 | 633/1104 | chr14 | 70735975 | ||
| chr14:70738256
|
C | T | 2 | a0001c0002a0005c0012 | 71 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
synonymous_variant | LOW | c.1833G>A | p.Ser611Ser | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/12 | 2175/11511 | 1833/3315 | 611/1104 | chr14 | 70738256 | ||
| chr14:70742562
|
C | G | 1 | a0001c0011 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.1356G>C | p.Thr452Thr | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/12 | 1698/11511 | 1356/3315 | 452/1104 | chr14 | 70742562 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:70722696
|
AGGAAAG | A | 24 | a0001c0002t0001a0001c0002t0008a0001c0002t0016others(21): Show | 80 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*7678_*7683delCTTT others(2): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 7678 | chr14 | 70722696 | |||||
| chr14:70722704
|
ACCTGGT | A | 24 | a0001c0002t0001a0001c0002t0008a0001c0002t0016others(21): Show | 80 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*7670_*7675delACCA others(2): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 7670 | chr14 | 70722704 | |||||
| chr14:70722705
|
C | T | 2 | a0001c0001t0026a0001c0001t0080 | 4 | HG01256.hp2 HG01258.hp2 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7675G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 7675 | chr14 | 70722705 | |||||
| chr14:70722744
|
T | G | 1 | a0001c0001t0047 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7636A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 7636 | chr14 | 70722744 | |||||
| chr14:70723037
|
G | T | 46 | a0001c0001t0002a0001c0001t0013a0001c0001t0021others(43): Show | 140 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*7343C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 7343 | chr14 | 70723037 | |||||
| chr14:70723199
|
A | G | 120 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(117): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
3_prime_UTR_variant | MODIFIER | c.*7181T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 7181 | chr14 | 70723199 | |||||
| chr14:70723242
|
A | C | 1 | a0001c0001t0013 | 4 | NA18950.hp1 NA18978.hp2 NA18995.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7138T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 7138 | chr14 | 70723242 | |||||
| chr14:70723385
|
A | G | 1 | a0001c0001t0065 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6995T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6995 | chr14 | 70723385 | |||||
| chr14:70723412
|
C | A | 6 | a0001c0001t0072a0001c0001t0073a0001c0001t0074others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6968G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6968 | chr14 | 70723412 | |||||
| chr14:70723435
|
T | G | 1 | a0001c0001t0112 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6945A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6945 | chr14 | 70723435 | |||||
| chr14:70723557
|
C | T | 2 | a0001c0009t0033a0001c0011t0051 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6823G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6823 | chr14 | 70723557 | |||||
| chr14:70723584
|
T | G | 2 | a0001c0009t0033a0001c0011t0051 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6796A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6796 | chr14 | 70723584 | |||||
| chr14:70723744
|
T | TTA | 2 | a0001c0009t0033a0001c0011t0051 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6634_*6635dupTA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6635 | chr14 | 70723744 | |||||
| chr14:70723770
|
G | A | 1 | a0001c0009t0033 | 2 | HG00099.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6610C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6610 | chr14 | 70723770 | |||||
| chr14:70723809
|
T | A | 8 | a0001c0001t0007a0001c0001t0028a0001c0001t0113others(5): Show | 19 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*6571A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6571 | chr14 | 70723809 | |||||
| chr14:70724366
|
C | T | 1 | a0001c0001t0078 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6014G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6014 | chr14 | 70724366 | |||||
| chr14:70724392
|
C | T | 2 | a0003c0007t0064a0003c0007t0096 | 2 | HG01109.hp2 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5988G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5988 | chr14 | 70724392 | |||||
| chr14:70724413
|
A | G | 3 | a0001c0001t0072a0001c0001t0073a0001c0001t0074 | 3 | HG02486.hp1 HG02622.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5967T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5967 | chr14 | 70724413 | |||||
| chr14:70724415
|
T | C | 1 | a0001c0002t0061 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5965A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5965 | chr14 | 70724415 | |||||
| chr14:70724469
|
G | C | 1 | a0001c0002t0061 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5911C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5911 | chr14 | 70724469 | |||||
| chr14:70724499
|
G | A | 2 | a0001c0003t0109a0012c0022t0094 | 2 | HG02055.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5881C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5881 | chr14 | 70724499 | |||||
| chr14:70724540
|
C | CA | 57 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(54): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*5839dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5839 | chr14 | 70724540 | |||||
| chr14:70724653
|
A | G | 1 | a0001c0011t0051 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5727T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5727 | chr14 | 70724653 | |||||
| chr14:70724706
|
C | T | 47 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(44): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*5674G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5674 | chr14 | 70724706 | |||||
| chr14:70724720
|
C | T | 1 | a0001c0002t0029 | 2 | HG02622.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5660G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5660 | chr14 | 70724720 | |||||
| chr14:70724777
|
G | A | 2 | a0001c0001t0091a0001c0001t0104 | 2 | HG00140.hp1 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5603C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5603 | chr14 | 70724777 | |||||
| chr14:70724856
|
G | A | 1 | a0001c0001t0057 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5524C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5524 | chr14 | 70724856 | |||||
| chr14:70724916
|
C | G | 6 | a0001c0001t0072a0001c0001t0073a0001c0001t0074others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5464G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5464 | chr14 | 70724916 | |||||
| chr14:70725064
|
G | A | 1 | a0001c0011t0051 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5316C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5316 | chr14 | 70725064 | |||||
| chr14:70725157
|
C | A | 1 | a0001c0001t0092 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5223G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5223 | chr14 | 70725157 | |||||
| chr14:70725178
|
C | G | 1 | a0001c0018t0083 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5202G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5202 | chr14 | 70725178 | |||||
| chr14:70725236
|
C | A | 3 | a0001c0001t0054a0001c0006t0017a0001c0021t0071 | 6 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5144G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5144 | chr14 | 70725236 | |||||
| chr14:70725243
|
C | T | 1 | a0001c0011t0051 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5137G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5137 | chr14 | 70725243 | |||||
| chr14:70725424
|
A | G | 3 | a0001c0002t0022a0001c0002t0059a0001c0002t0060 | 5 | HG02723.hp1 HG02970.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4956T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 4956 | chr14 | 70725424 | |||||
| chr14:70725722
|
A | G | 3 | a0001c0001t0021a0001c0001t0039a0001c0001t0045 | 5 | HG00408.hp1 HG00597.hp1 NA18939.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4658T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 4658 | chr14 | 70725722 | |||||
| chr14:70725810
|
C | T | 6 | a0001c0001t0007a0001c0001t0028a0001c0001t0113others(3): Show | 17 | HG00733.hp1 HG01884.hp1 HG02647.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4570G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 4570 | chr14 | 70725810 | |||||
| chr14:70725823
|
G | A | 59 | a0001c0001t0002a0001c0001t0007a0001c0001t0012others(56): Show | 169 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*4557C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 4557 | chr14 | 70725823 | |||||
| chr14:70725830
|
T | TCA | 10 | a0001c0001t0009a0001c0001t0052a0001c0001t0073others(7): Show | 19 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4548_*4549dupTG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 4549 | chr14 | 70725830 | |||||
| chr14:70725830
|
TCA | T | 49 | a0001c0001t0002a0001c0001t0012a0001c0001t0013others(46): Show | 147 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*4548_*4549delTG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 4548 | chr14 | 70725830 | |||||
| chr14:70726075
|
G | A | 1 | a0001c0001t0112 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4305C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 4305 | chr14 | 70726075 | |||||
| chr14:70726398
|
T | C | 2 | a0001c0001t0100a0001c0001t0110 | 2 | HG03834.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3982A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3982 | chr14 | 70726398 | |||||
| chr14:70726554
|
G | T | 1 | a0001c0001t0081 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3826C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3826 | chr14 | 70726554 | |||||
| chr14:70726586
|
A | G | 48 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(45): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*3794T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3794 | chr14 | 70726586 | |||||
| chr14:70726588
|
T | G | 1 | a0001c0009t0033 | 2 | HG00099.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3792A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3792 | chr14 | 70726588 | |||||
| chr14:70726629
|
T | C | 1 | a0001c0001t0069 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3751A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3751 | chr14 | 70726629 | |||||
| chr14:70726699
|
C | T | 9 | a0001c0001t0002a0001c0001t0013a0001c0001t0021others(6): Show | 43 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3681G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3681 | chr14 | 70726699 | |||||
| chr14:70726726
|
A | C | 4 | a0001c0001t0055a0001c0002t0022a0001c0002t0059others(1): Show | 6 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3654T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3654 | chr14 | 70726726 | |||||
| chr14:70727081
|
C | G | 1 | a0001c0001t0115 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3299G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3299 | chr14 | 70727081 | |||||
| chr14:70727156
|
C | T | 2 | a0001c0001t0034a0001c0001t0069 | 3 | HG02630.hp2 HG02897.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3224G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3224 | chr14 | 70727156 | |||||
| chr14:70727412
|
T | C | 1 | a0001c0001t0066 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2968A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2968 | chr14 | 70727412 | |||||
| chr14:70727436
|
C | T | 12 | a0001c0001t0009a0001c0001t0011a0001c0001t0052others(9): Show | 26 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2944G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2944 | chr14 | 70727436 | |||||
| chr14:70727456
|
C | G | 1 | a0001c0001t0085 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2924G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2924 | chr14 | 70727456 | |||||
| chr14:70727495
|
C | T | 2 | a0003c0007t0064a0003c0007t0096 | 2 | HG01109.hp2 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2885G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2885 | chr14 | 70727495 | |||||
| chr14:70727518
|
T | C | 1 | a0001c0001t0112 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2862A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2862 | chr14 | 70727518 | |||||
| chr14:70727606
|
T | C | 8 | a0001c0001t0015a0001c0001t0031a0001c0001t0057others(5): Show | 11 | HG01074.hp1 HG01433.hp2 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2774A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2774 | chr14 | 70727606 | |||||
| chr14:70727722
|
G | C | 1 | a0001c0001t0054 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2658C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2658 | chr14 | 70727722 | |||||
| chr14:70727997
|
C | A | 1 | a0001c0011t0051 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2383G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2383 | chr14 | 70727997 | |||||
| chr14:70728014
|
C | T | 2 | a0001c0002t0032a0001c0002t0042 | 3 | HG02040.hp1 HG02083.hp2 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2366G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2366 | chr14 | 70728014 | |||||
| chr14:70728057
|
C | T | 111 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(108): Show | 298 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(295): Show |
3_prime_UTR_variant | MODIFIER | c.*2323G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2323 | chr14 | 70728057 | |||||
| chr14:70728088
|
C | T | 1 | a0001c0002t0060 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2292G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2292 | chr14 | 70728088 | |||||
| chr14:70728104
|
CAG | C | 2 | a0001c0006t0017a0001c0021t0071 | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2274_*2275delCT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2274 | chr14 | 70728104 | |||||
| chr14:70728113
|
C | CT | 15 | a0001c0001t0002a0001c0001t0013a0001c0001t0021others(12): Show | 56 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2266dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2266 | chr14 | 70728113 | |||||
| chr14:70728113
|
C | CTT | 27 | a0001c0001t0025a0001c0001t0045a0001c0001t0046others(24): Show | 72 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2265_*2266dupAA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2266 | chr14 | 70728113 | |||||
| chr14:70728113
|
C | CTTT | 13 | a0001c0001t0037a0001c0001t0074a0001c0001t0075others(10): Show | 22 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2264_*2266dupAAA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2266 | chr14 | 70728113 | |||||
| chr14:70728113
|
C | CTTTT | 31 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(28): Show | 104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2263_*2266dupAAAA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2266 | chr14 | 70728113 | |||||
| chr14:70728113
|
C | CTTTTT | 16 | a0001c0001t0018a0001c0001t0031a0001c0001t0036others(13): Show | 20 | HG00735.hp2 HG01361.hp1 HG01433.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2262_*2266dupAAAA others(1): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2266 | chr14 | 70728113 | |||||
| chr14:70728113
|
C | CTTTTTT | 3 | a0001c0001t0079a0001c0001t0101a0001c0006t0017 | 6 | HG00735.hp1 HG01346.hp1 HG01884.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2261_*2266dupAAAA others(2): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2266 | chr14 | 70728113 | |||||
| chr14:70728113
|
CTTTTTTT others(7): Show |
C | 9 | a0001c0001t0007a0001c0001t0012a0001c0001t0028others(6): Show | 24 | HG00733.hp1 HG01106.hp2 HG01884.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2253_*2266delAAAA others(10): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2253 | chr14 | 70728113 | |||||
| chr14:70728197
|
C | T | 1 | a0001c0011t0051 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2183G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2183 | chr14 | 70728197 | |||||
| chr14:70728246
|
C | T | 1 | a0001c0001t0088 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2134G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2134 | chr14 | 70728246 | |||||
| chr14:70728381
|
C | T | 1 | a0001c0001t0087 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1999G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1999 | chr14 | 70728381 | |||||
| chr14:70728413
|
C | T | 10 | a0001c0001t0002a0001c0001t0013a0001c0001t0021others(7): Show | 45 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1967G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1967 | chr14 | 70728413 | |||||
| chr14:70728442
|
A | T | 1 | a0001c0001t0085 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1938T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1938 | chr14 | 70728442 | |||||
| chr14:70728491
|
C | T | 1 | a0001c0002t0050 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1889G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1889 | chr14 | 70728491 | |||||
| chr14:70728635
|
G | A | 1 | a0001c0001t0113 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1745C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1745 | chr14 | 70728635 | |||||
| chr14:70728795
|
C | T | 2 | a0001c0001t0076a0001c0001t0115 | 2 | HG01192.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1585G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1585 | chr14 | 70728795 | |||||
| chr14:70728990
|
C | T | 1 | a0001c0001t0100 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1390G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1390 | chr14 | 70728990 | |||||
| chr14:70729101
|
T | A | 2 | a0001c0001t0114a0001c0005t0098 | 2 | HG03453.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1279A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1279 | chr14 | 70729101 | |||||
| chr14:70729171
|
C | T | 5 | a0001c0001t0072a0001c0001t0073a0001c0001t0074others(2): Show | 5 | HG01192.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1209G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1209 | chr14 | 70729171 | |||||
| chr14:70729182
|
G | A | 1 | a0001c0018t0083 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1198C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1198 | chr14 | 70729182 | |||||
| chr14:70729252
|
G | A | 2 | a0001c0001t0076a0001c0001t0115 | 2 | HG01192.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1128C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1128 | chr14 | 70729252 | |||||
| chr14:70729301
|
A | G | 1 | a0001c0003t0049 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1079T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1079 | chr14 | 70729301 | |||||
| chr14:70729310
|
T | C | 1 | a0001c0002t0068 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1070A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1070 | chr14 | 70729310 | |||||
| chr14:70729357
|
A | G | 1 | a0001c0001t0099 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1023T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1023 | chr14 | 70729357 | |||||
| chr14:70729563
|
C | T | 1 | a0001c0005t0098 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*817G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 817 | chr14 | 70729563 | |||||
| chr14:70729625
|
G | A | 3 | a0001c0001t0034a0001c0001t0069a0001c0018t0083 | 4 | HG00609.hp1 HG02630.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*755C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 755 | chr14 | 70729625 | |||||
| chr14:70729670
|
T | C | 2 | a0001c0002t0016a0001c0002t0070 | 5 | HG02015.hp2 HG02132.hp1 NA18980.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*710A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 710 | chr14 | 70729670 | |||||
| chr14:70729710
|
C | T | 10 | a0001c0001t0002a0001c0001t0013a0001c0001t0021others(7): Show | 45 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*670G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 670 | chr14 | 70729710 | |||||
| chr14:70729771
|
G | C | 8 | a0001c0001t0072a0001c0001t0073a0001c0001t0074others(5): Show | 11 | HG01192.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*609C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 609 | chr14 | 70729771 | |||||
| chr14:70729988
|
C | T | 1 | a0001c0002t0029 | 2 | HG02622.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*392G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 392 | chr14 | 70729988 | |||||
| chr14:70730022
|
G | A | 6 | a0001c0001t0072a0001c0001t0073a0001c0001t0074others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*358C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 358 | chr14 | 70730022 | |||||
| chr14:70730034
|
G | A | 5 | a0001c0001t0025a0001c0001t0077a0001c0001t0078others(2): Show | 5 | HG02145.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*346C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 346 | chr14 | 70730034 | |||||
| chr14:70809261
|
A | AC | 20 | a0001c0001t0027a0001c0001t0028a0001c0001t0039others(17): Show | 23 | HG00597.hp1 HG01081.hp2 HG01496.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-91dupG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 91 | chr14 | 70809261 | |||||
| chr14:70809268
|
C | A | 1 | a0001c0001t0019 | 4 | NA18941.hp1 NA18960.hp2 NA18998.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-97G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 97 | chr14 | 70809268 | |||||
| chr14:70809268
|
C | G | 3 | a0001c0001t0010a0001c0001t0085a0001c0001t0086 | 11 | NA18949.hp2 NA18964.hp1 NA18968.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-97G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 97 | chr14 | 70809268 | |||||
| chr14:70809269
|
C | A | 10 | a0001c0001t0003a0001c0001t0018a0001c0001t0026others(7): Show | 41 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(38): Show |
5_prime_UTR_variant | MODIFIER | c.-98G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 98 | chr14 | 70809269 | |||||
| chr14:70809269
|
C | G | 4 | a0001c0001t0035a0001c0001t0084a0001c0002t0020others(1): Show | 7 | HG00438.hp2 HG02083.hp1 NA18967.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-98G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 98 | chr14 | 70809269 | |||||
| chr14:70809361
|
G | A | 1 | a0001c0018t0083 | 1 | HG00609.hp1 | 5_prime_UTR_variant | MODIFIER | c.-190C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 190 | chr14 | 70809361 | |||||
| chr14:70809489
|
A | C | 80 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(77): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
5_prime_UTR_variant | MODIFIER | c.-318T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 318 | chr14 | 70809489 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:70731038
|
T | G | 286 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(283): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2831-174A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731038 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6079): Show |
1 | a0001c0002t0001g0103 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6088): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6058): Show |
1 | a0001c0002t0070g0092 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6067): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6052): Show |
1 | a0001c0002t0001g0081 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6061): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6087): Show |
1 | a0001c0002t0001g0072 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6096): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6045): Show |
2 | a0001c0002t0001g0096a0001c0002t0001g0097 | 2 | NA18947.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6054): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6054): Show |
4 | a0001c0002t0001g0093a0001c0002t0001g0098a0001c0002t0001g0099others(1): Show | 4 | HG00621.hp1 HG02071.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6063): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6055): Show |
1 | a0001c0002t0001g0094 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6064): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6057): Show |
4 | a0001c0002t0001g0100a0001c0002t0020g0003a0001c0002t0020g0013others(1): Show | 5 | HG02683.hp1 NA18967.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6066): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6058): Show |
3 | a0001c0002t0016g0005a0001c0002t0016g0089a0001c0002t0016g0091 | 4 | HG02015.hp2 HG02132.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6067): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6063): Show |
1 | a0001c0002t0008g0171 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6072): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6066): Show |
2 | a0001c0002t0001g0175a0001c0002t0008g0118 | 2 | HG02135.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6075): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6067): Show |
2 | a0001c0002t0001g0071a0001c0002t0001g0082 | 2 | HG03710.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6076): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6068): Show |
1 | a0001c0002t0008g0080 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6077): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6070): Show |
1 | a0001c0002t0001g0119 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6079): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6076): Show |
1 | a0001c0002t0023g0107 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6085): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6077): Show |
4 | a0001c0002t0001g0105a0001c0002t0001g0106a0001c0002t0001g0109others(1): Show | 4 | HG00639.hp1 HG01167.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6086): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6078): Show |
4 | a0001c0002t0001g0007a0001c0002t0001g0075a0001c0002t0001g0108others(1): Show | 5 | HG01358.hp2 HG02273.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6087): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6079): Show |
1 | a0001c0002t0001g0104 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6088): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6080): Show |
1 | a0001c0002t0062g0079 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6089): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6083): Show |
1 | a0001c0002t0001g0004 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6092): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6084): Show |
1 | a0001c0002t0061g0095 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6093): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6085): Show |
1 | a0001c0002t0001g0176 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6094): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6092): Show |
1 | a0001c0002t0001g0088 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6101): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6093): Show |
1 | a0001c0002t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6102): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6078): Show |
1 | a0001c0002t0032g0178 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6087): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6079): Show |
2 | a0001c0002t0032g0078a0001c0002t0042g0016 | 2 | HG02040.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6088): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6050): Show |
1 | a0001c0002t0008g0076 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6059): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6078): Show |
1 | a0001c0002t0001g0110 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6087): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6077): Show |
1 | a0001c0002t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6086): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6084): Show |
1 | a0001c0002t0001g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6093): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6060): Show |
1 | a0001c0002t0008g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6069): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6060): Show |
1 | a0001c0002t0068g0101 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6069): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731059
|
T | TAAGAATA others(6091): Show |
1 | a0001c0002t0001g0102 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6100): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | ||||||
| chr14:70731138
|
C | T | 1 | a0001c0002t0001g0075 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2831-274G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731138 | ||||||
| chr14:70731142
|
T | C | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2831-278A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731142 | ||||||
| chr14:70731355
|
A | C | 77 | a0001c0001t0055g0085a0001c0001t0095g0258a0001c0002t0001g0004others(74): Show | 82 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.2831-491T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731355 | ||||||
| chr14:70731494
|
C | T | 1 | a0001c0002t0008g0080 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2831-630G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731494 | ||||||
| chr14:70731518
|
C | T | 1 | a0004c0020t0108g0334 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2831-654G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731518 | ||||||
| chr14:70731525
|
G | A | 1 | a0001c0002t0001g0111 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2831-661C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731525 | ||||||
| chr14:70731624
|
A | C | 1 | a0001c0001t0006g0154 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2831-760T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731624 | ||||||
| chr14:70731650
|
T | C | 1 | a0001c0002t0008g0080 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2831-786A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731650 | ||||||
| chr14:70731834
|
C | T | 143 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(140): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.2830+705G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731834 | ||||||
| chr14:70731953
|
T | G | 4 | a0001c0002t0022g0022a0001c0002t0022g0023a0001c0002t0059g0024others(1): Show | 4 | HG02723.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2830+586A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731953 | ||||||
| chr14:70732041
|
T | C | 42 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(39): Show | 45 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(42): Show |
intron_variant | MODIFIER | c.2830+498A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70732041 | ||||||
| chr14:70732050
|
G | A | 1 | a0001c0001t0030g0168 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2830+489C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70732050 | ||||||
| chr14:70732316
|
G | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2830+223C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70732316 | ||||||
| chr14:70732357
|
C | A | 1 | a0012c0022t0094g0259 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2830+182G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70732357 | ||||||
| chr14:70732422
|
G | A | 2 | a0001c0001t0114g0321a0001c0005t0098g0320 | 2 | HG03453.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2830+117C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70732422 | ||||||
| chr14:70733450
|
G | T | 1 | a0001c0001t0005g0315 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2027-108C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70733450 | ||||||
| chr14:70733700
|
G | A | 1 | a0001c0002t0001g0104 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2027-358C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70733700 | ||||||
| chr14:70733724
|
T | C | 1 | a0001c0001t0004g0351 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2027-382A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70733724 | ||||||
| chr14:70733727
|
G | C | 4 | a0001c0001t0041g0018a0001c0005t0005g0323a0001c0005t0005g0324others(1): Show | 4 | HG01081.hp2 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2027-385C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70733727 | ||||||
| chr14:70733960
|
G | A | 1 | a0001c0004t0067g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2026+426C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70733960 | ||||||
| chr14:70734096
|
C | A | 5 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2026+290G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70734096 | ||||||
| chr14:70734215
|
T | C | 287 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(284): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2026+171A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70734215 | ||||||
| chr14:70734373
|
G | A | 2 | a0001c0002t0001g0176a0001c0002t0008g0171 | 2 | NA18998.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2026+13C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70734373 | ||||||
| chr14:70734642
|
C | A | 2 | a0001c0001t0005g0011a0001c0001t0005g0314 | 3 | NA18945.hp1 NA18970.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1914-144G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70734642 | ||||||
| chr14:70734734
|
A | C | 76 | a0001c0001t0055g0085a0001c0002t0001g0004a0001c0002t0001g0007others(73): Show | 81 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1914-236T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70734734 | ||||||
| chr14:70734924
|
C | T | 24 | a0001c0001t0007g0266a0001c0001t0007g0270a0001c0001t0007g0274others(21): Show | 24 | HG00733.hp1 HG01106.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1914-426G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70734924 | ||||||
| chr14:70735021
|
C | A | 11 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(8): Show | 11 | HG01192.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1914-523G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735021 | ||||||
| chr14:70735050
|
A | T | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1914-552T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735050 | ||||||
| chr14:70735087
|
C | T | 313 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(310): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1914-589G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735087 | ||||||
| chr14:70735252
|
G | T | 1 | a0001c0001t0003g0222 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1913+709C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735252 | ||||||
| chr14:70735366
|
CT | C | 194 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(191): Show | 205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1913+594delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735366 | ||||||
| chr14:70735376
|
T | A | 1 | a0001c0001t0021g0122 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1913+585A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735376 | ||||||
| chr14:70735535
|
T | G | 7 | a0001c0001t0025g0025a0001c0001t0077g0183a0001c0001t0078g0182others(4): Show | 7 | HG02145.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1913+426A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735535 | ||||||
| chr14:70735609
|
C | T | 1 | a0001c0002t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1913+352G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735609 | ||||||
| chr14:70735610
|
G | C | 7 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(4): Show | 7 | HG00639.hp1 HG01070.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.1913+351C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735610 | ||||||
| chr14:70735614
|
C | T | 1 | a0001c0001t0054g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1913+347G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735614 | ||||||
| chr14:70735933
|
C | T | 287 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(284): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1913+28G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735933 | ||||||
| chr14:70736118
|
ACAC | A | 66 | a0001c0002t0001g0004a0001c0002t0001g0007a0001c0002t0001g0066others(63): Show | 71 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1845-92_1845-90del others(3): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736118 | ||||||
| chr14:70736266
|
C | A | 1 | a0001c0001t0092g0251 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1845-237G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736266 | ||||||
| chr14:70736352
|
C | T | 1 | a0001c0002t0016g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1845-323G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736352 | ||||||
| chr14:70736393
|
G | A | 1 | a0001c0001t0004g0343 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1845-364C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736393 | ||||||
| chr14:70736405
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1845-376C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736405 | ||||||
| chr14:70736406
|
T | A | 3 | a0001c0001t0007g0266a0001c0001t0007g0283a0001c0001t0007g0295 | 3 | HG02895.hp1 HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1845-377A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736406 | ||||||
| chr14:70736514
|
T | C | 24 | a0001c0001t0007g0266a0001c0001t0007g0270a0001c0001t0007g0274others(21): Show | 24 | HG00733.hp1 HG01106.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1845-485A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736514 | ||||||
| chr14:70736786
|
C | G | 24 | a0001c0001t0007g0266a0001c0001t0007g0270a0001c0001t0007g0274others(21): Show | 24 | HG00733.hp1 HG01106.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1845-757G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736786 | ||||||
| chr14:70737036
|
T | C | 1 | a0001c0002t0023g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1845-1007A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737036 | ||||||
| chr14:70737149
|
A | G | 1 | a0001c0001t0034g0130 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1844+1096T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737149 | ||||||
| chr14:70737168
|
G | A | 4 | a0001c0001t0007g0274a0001c0001t0007g0285a0001c0001t0028g0244others(1): Show | 4 | HG00733.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1844+1077C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737168 | ||||||
| chr14:70737176
|
C | G | 2 | a0001c0001t0100g0340a0001c0001t0110g0332 | 2 | HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1844+1069G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737176 | ||||||
| chr14:70737448
|
G | C | 120 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(117): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1844+797C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737448 | ||||||
| chr14:70737545
|
C | T | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1844+700G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737545 | ||||||
| chr14:70737557
|
G | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1844+688C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737557 | ||||||
| chr14:70737652
|
G | A | 254 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(251): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.1844+593C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737652 | ||||||
| chr14:70737833
|
T | C | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1844+412A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737833 | ||||||
| chr14:70738412
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1691-14C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70738412 | ||||||
| chr14:70738419
|
A | G | 24 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0147others(21): Show | 24 | HG00280.hp1 HG01256.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.1691-21T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70738419 | ||||||
| chr14:70738626
|
C | G | 1 | a0001c0001t0006g0156 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1691-228G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70738626 | ||||||
| chr14:70738713
|
T | C | 43 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(40): Show | 47 | HG00408.hp1 HG00597.hp1 HG01256.hp2 others(44): Show |
intron_variant | MODIFIER | c.1691-315A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70738713 | ||||||
| chr14:70738805
|
G | T | 1 | a0001c0002t0001g0102 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1691-407C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70738805 | ||||||
| chr14:70738947
|
C | T | 2 | a0003c0007t0064g0150a0003c0007t0096g0257 | 2 | HG01109.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1691-549G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70738947 | ||||||
| chr14:70739010
|
T | C | 95 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(92): Show | 98 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1691-612A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739010 | ||||||
| chr14:70739031
|
A | G | 1 | a0001c0001t0009g0292 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1691-633T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739031 | ||||||
| chr14:70739090
|
C | T | 1 | a0001c0003t0001g0077 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1691-692G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739090 | ||||||
| chr14:70739286
|
T | C | 1 | a0001c0002t0001g0102 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1690+756A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739286 | ||||||
| chr14:70739379
|
C | T | 1 | a0001c0001t0009g0355 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1690+663G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739379 | ||||||
| chr14:70739502
|
T | TCA | 178 | a0001c0001t0002g0001a0001c0001t0002g0036a0001c0001t0002g0037others(175): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1690+538_1690+539d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739502 | ||||||
| chr14:70739502
|
T | TCACA | 25 | a0001c0001t0005g0264a0001c0001t0005g0301a0001c0001t0005g0315others(22): Show | 26 | HG00099.hp1 HG00639.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1690+536_1690+539d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739502 | ||||||
| chr14:70739502
|
T | TCACACA | 3 | a0001c0001t0099g0284a0001c0002t0001g0108a0001c0003t0056g0067 | 3 | HG01346.hp2 HG01358.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1690+534_1690+539d others(8): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739502 | ||||||
| chr14:70739502
|
T | TCACACAC others(11): Show |
1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1690+522_1690+539d others(20): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739502 | ||||||
| chr14:70739502
|
TCA | T | 17 | a0001c0001t0003g0222a0001c0001t0004g0337a0001c0001t0004g0338others(14): Show | 17 | HG02572.hp1 HG03017.hp1 HG03130.hp2 others(14): Show |
intron_variant | MODIFIER | c.1690+538_1690+539d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739502 | ||||||
| chr14:70739525
|
C | CACTT | 5 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1690+513_1690+516d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739525 | ||||||
| chr14:70739546
|
A | T | 198 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(195): Show | 209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.1690+496T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739546 | ||||||
| chr14:70739558
|
C | A | 189 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(186): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1690+484G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739558 | ||||||
| chr14:70739834
|
G | C | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1690+208C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739834 | ||||||
| chr14:70740200
|
C | T | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-36G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70740200 | ||||||
| chr14:70740377
|
G | A | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1568-213C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70740377 | ||||||
| chr14:70740475
|
T | C | 5 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1568-311A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70740475 | ||||||
| chr14:70740569
|
A | G | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1568-405T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70740569 | ||||||
| chr14:70740577
|
T | C | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1568-413A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70740577 | ||||||
| chr14:70740675
|
G | A | 1 | a0001c0002t0029g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1568-511C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70740675 | ||||||
| chr14:70740883
|
C | T | 2 | a0001c0001t0026g0201a0001c0001t0026g0223 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1568-719G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70740883 | ||||||
| chr14:70741096
|
C | CT | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-933dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741096 | ||||||
| chr14:70741161
|
G | A | 98 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(95): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1568-997C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741161 | ||||||
| chr14:70741186
|
G | A | 2 | a0001c0001t0055g0085a0001c0002t0022g0084 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1568-1022C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741186 | ||||||
| chr14:70741251
|
C | T | 1 | a0001c0002t0001g0071 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1568-1087G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741251 | ||||||
| chr14:70741310
|
G | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1567+1041C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741310 | ||||||
| chr14:70741336
|
C | T | 53 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0002t0001g0004others(50): Show | 57 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1567+1015G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741336 | ||||||
| chr14:70741504
|
A | G | 4 | a0001c0001t0003g0002a0001c0001t0003g0195a0001c0001t0003g0196others(1): Show | 6 | NA18947.hp2 NA18953.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.1567+847T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741504 | ||||||
| chr14:70741505
|
T | C | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1567+846A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741505 | ||||||
| chr14:70741594
|
T | G | 1 | a0001c0001t0002g0063 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1567+757A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741594 | ||||||
| chr14:70741840
|
G | A | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1567+511C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741840 | ||||||
| chr14:70741870
|
C | T | 1 | a0001c0002t0050g0068 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1567+481G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741870 | ||||||
| chr14:70741968
|
C | A | 1 | a0011c0010t0003g0209 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1567+383G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741968 | ||||||
| chr14:70741976
|
T | C | 1 | a0001c0005t0005g0323 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1567+375A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741976 | ||||||
| chr14:70741997
|
G | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1567+354C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741997 | ||||||
| chr14:70742094
|
G | C | 2 | a0001c0001t0055g0085a0001c0002t0022g0084 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1567+257C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70742094 | ||||||
| chr14:70742210
|
C | T | 1 | a0001c0001t0003g0222 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1567+141G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70742210 | ||||||
| chr14:70742279
|
A | G | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1567+72T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70742279 | ||||||
| chr14:70742308
|
C | A | 104 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(101): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1567+43G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70742308 | ||||||
| chr14:70742610
|
C | T | 1 | a0001c0001t0074g0188 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1327-19G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742610 | ||||||
| chr14:70742768
|
G | T | 1 | a0001c0001t0005g0316 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1327-177C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742768 | ||||||
| chr14:70742851
|
G | C | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1327-260C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742851 | ||||||
| chr14:70742901
|
T | TTATATAT others(7): Show |
2 | a0001c0006t0017g0141a0001c0006t0017g0165 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1327-311_1327-310i others(16): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742901 | ||||||
| chr14:70742901
|
T | TTATATAT others(13): Show |
1 | a0001c0006t0017g0140 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1327-311_1327-310i others(22): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742901 | ||||||
| chr14:70742911
|
T | A | 5 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-320A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742911 | ||||||
| chr14:70742911
|
T | TTA | 3 | a0001c0001t0004g0343a0001c0001t0100g0340a0001c0003t0109g0327 | 3 | HG02895.hp2 HG03834.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1327-322_1327-321d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742911 | ||||||
| chr14:70742911
|
T | TTATA | 4 | a0001c0001t0110g0332a0001c0009t0033g0123a0001c0009t0033g0124others(1): Show | 4 | HG00099.hp2 HG04115.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327-324_1327-321d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742911 | ||||||
| chr14:70742911
|
TTA | T | 93 | a0001c0001t0002g0001a0001c0001t0002g0036a0001c0001t0002g0037others(90): Show | 96 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1327-322_1327-321d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742911 | ||||||
| chr14:70742911
|
TTATA | T | 162 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(159): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1327-324_1327-321d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742911 | ||||||
| chr14:70742911
|
TTATATA | T | 60 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(57): Show | 63 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.1327-326_1327-321d others(8): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742911 | ||||||
| chr14:70743233
|
C | T | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1327-642G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743233 | ||||||
| chr14:70743279
|
C | T | 2 | a0001c0018t0083g0228a0001c0021t0071g0143 | 2 | HG00609.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1327-688G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743279 | ||||||
| chr14:70743498
|
A | G | 1 | a0001c0011t0051g0184 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1327-907T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743498 | ||||||
| chr14:70743523
|
A | C | 2 | a0001c0001t0007g0266a0001c0001t0007g0283 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1327-932T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743523 | ||||||
| chr14:70743699
|
G | C | 6 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(3): Show | 6 | HG00609.hp1 HG01884.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1327-1108C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743699 | ||||||
| chr14:70743712
|
C | A | 1 | a0001c0001t0041g0018 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1327-1121G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743712 | ||||||
| chr14:70743766
|
A | G | 2 | a0001c0002t0001g0102a0001c0002t0068g0101 | 2 | HG02155.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1327-1175T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743766 | ||||||
| chr14:70743827
|
C | T | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1327-1236G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743827 | ||||||
| chr14:70743846
|
C | T | 1 | a0011c0010t0003g0209 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1327-1255G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743846 | ||||||
| chr14:70743854
|
G | A | 2 | a0001c0002t0001g0105a0001c0002t0001g0106 | 2 | HG00639.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1327-1263C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743854 | ||||||
| chr14:70743905
|
C | T | 2 | a0001c0002t0070g0092a0001c0003t0056g0067 | 2 | HG03098.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1327-1314G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743905 | ||||||
| chr14:70744039
|
T | G | 5 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-1448A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744039 | ||||||
| chr14:70744180
|
G | A | 1 | a0001c0001t0004g0354 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1327-1589C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744180 | ||||||
| chr14:70744200
|
G | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1327-1609C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744200 | ||||||
| chr14:70744289
|
T | A | 1 | a0001c0002t0008g0080 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1327-1698A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744289 | ||||||
| chr14:70744362
|
TA | T | 7 | a0001c0001t0012g0020a0001c0001t0012g0030a0001c0001t0012g0031others(4): Show | 7 | HG01891.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1327-1772delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744362 | ||||||
| chr14:70744375
|
A | G | 1 | a0001c0001t0004g0305 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1327-1784T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744375 | ||||||
| chr14:70744421
|
G | C | 1 | a0001c0001t0034g0129 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1327-1830C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744421 | ||||||
| chr14:70744505
|
T | G | 1 | a0001c0002t0008g0080 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1327-1914A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744505 | ||||||
| chr14:70744636
|
C | T | 28 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0147others(25): Show | 28 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1327-2045G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744636 | ||||||
| chr14:70744981
|
AGCACTGA others(7): Show |
A | 1 | a0001c0001t0002g0053 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1327-2404_1327-239 others(18): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744981 | ||||||
| chr14:70745052
|
C | T | 1 | a0001c0001t0004g0350 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1327-2461G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745052 | ||||||
| chr14:70745074
|
T | A | 1 | a0001c0001t0002g0053 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1327-2483A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745074 | ||||||
| chr14:70745212
|
C | T | 1 | a0006c0014t0015g0135 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1327-2621G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745212 | ||||||
| chr14:70745212
|
CT | C | 17 | a0001c0001t0006g0151a0001c0001t0006g0152a0001c0001t0006g0153others(14): Show | 17 | HG01256.hp1 HG01952.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1327-2622delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745212 | ||||||
| chr14:70745299
|
T | C | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1327-2708A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745299 | ||||||
| chr14:70745316
|
G | A | 1 | a0001c0001t0005g0317 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1327-2725C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745316 | ||||||
| chr14:70745441
|
A | G | 57 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(54): Show | 60 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.1327-2850T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745441 | ||||||
| chr14:70745475
|
C | T | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1327-2884G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745475 | ||||||
| chr14:70745504
|
G | A | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1327-2913C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745504 | ||||||
| chr14:70745511
|
G | T | 3 | a0001c0003t0008g0170a0001c0003t0008g0179a0001c0003t0056g0067 | 3 | HG03098.hp1 HG03540.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1327-2920C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745511 | ||||||
| chr14:70745663
|
G | A | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1327-3072C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745663 | ||||||
| chr14:70745669
|
T | C | 297 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(294): Show | 311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1327-3078A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745669 | ||||||
| chr14:70745731
|
C | A | 1 | a0001c0001t0010g0232 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1326+3098G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745731 | ||||||
| chr14:70745737
|
C | CA | 9 | a0001c0001t0044g0019a0001c0001t0072g0191a0001c0001t0073g0190others(6): Show | 9 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1326+3091dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745737 | ||||||
| chr14:70745752
|
T | G | 1 | a0001c0005t0098g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1326+3077A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745752 | ||||||
| chr14:70746007
|
A | C | 2 | a0001c0001t0007g0274a0001c0001t0007g0285 | 2 | HG00733.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1326+2822T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746007 | ||||||
| chr14:70746024
|
G | A | 1 | a0001c0005t0098g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1326+2805C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746024 | ||||||
| chr14:70746097
|
T | C | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1326+2732A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746097 | ||||||
| chr14:70746352
|
C | T | 1 | a0001c0001t0002g0040 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1326+2477G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746352 | ||||||
| chr14:70746356
|
T | C | 1 | a0001c0001t0004g0350 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1326+2473A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746356 | ||||||
| chr14:70746369
|
G | A | 297 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(294): Show | 311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1326+2460C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746369 | ||||||
| chr14:70746398
|
C | T | 56 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(53): Show | 59 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.1326+2431G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746398 | ||||||
| chr14:70746403
|
T | C | 1 | a0001c0001t0002g0053 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1326+2426A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746403 | ||||||
| chr14:70746473
|
A | G | 56 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(53): Show | 59 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.1326+2356T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746473 | ||||||
| chr14:70746497
|
A | G | 1 | a0001c0001t0003g0208 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1326+2332T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746497 | ||||||
| chr14:70746777
|
G | A | 1 | a0001c0002t0023g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1326+2052C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746777 | ||||||
| chr14:70746790
|
G | C | 1 | a0001c0005t0098g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1326+2039C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746790 | ||||||
| chr14:70746969
|
C | T | 2 | a0001c0001t0039g0014a0001c0001t0045g0045 | 2 | HG00597.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1326+1860G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746969 | ||||||
| chr14:70747154
|
T | C | 297 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(294): Show | 311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1326+1675A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70747154 | ||||||
| chr14:70747167
|
TG | T | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1326+1661delC | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70747167 | ||||||
| chr14:70747521
|
T | C | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1326+1308A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70747521 | ||||||
| chr14:70747550
|
G | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1326+1279C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70747550 | ||||||
| chr14:70747965
|
G | T | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1326+864C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70747965 | ||||||
| chr14:70747991
|
C | T | 1 | a0001c0002t0001g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1326+838G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70747991 | ||||||
| chr14:70748035
|
A | AG | 359 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(356): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1326+793dupC | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748035 | ||||||
| chr14:70748061
|
C | T | 1 | a0001c0011t0051g0184 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1326+768G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748061 | ||||||
| chr14:70748063
|
T | C | 297 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(294): Show | 311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1326+766A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748063 | ||||||
| chr14:70748104
|
C | CA | 165 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(162): Show | 171 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.1326+724dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748104 | ||||||
| chr14:70748104
|
C | CAA | 75 | a0001c0001t0005g0296a0001c0001t0052g0173a0001c0001t0053g0090others(72): Show | 80 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.1326+723_1326+724d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748104 | ||||||
| chr14:70748121
|
T | A | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1326+708A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748121 | ||||||
| chr14:70748123
|
G | A | 297 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(294): Show | 311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1326+706C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748123 | ||||||
| chr14:70748158
|
TC | T | 3 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188 | 3 | HG02486.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1326+670delG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748158 | ||||||
| chr14:70748253
|
T | C | 1 | a0001c0001t0005g0310 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1326+576A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748253 | ||||||
| chr14:70748314
|
C | T | 2 | a0001c0003t0008g0170a0001c0003t0008g0179 | 2 | HG03540.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1326+515G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748314 | ||||||
| chr14:70748514
|
A | G | 349 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(346): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1326+315T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748514 | ||||||
| chr14:70748532
|
G | A | 28 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0147others(25): Show | 28 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1326+297C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748532 | ||||||
| chr14:70748596
|
T | G | 1 | a0001c0002t0029g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1326+233A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748596 | ||||||
| chr14:70748663
|
T | G | 192 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(189): Show | 203 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1326+166A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748663 | ||||||
| chr14:70748677
|
T | G | 53 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0002t0001g0004others(50): Show | 57 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1326+152A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748677 | ||||||
| chr14:70748707
|
T | C | 1 | a0001c0001t0100g0340 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1326+122A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748707 | ||||||
| chr14:70748736
|
G | A | 2 | a0001c0011t0051g0184a0001c0013t0005g0282 | 2 | NA18979.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1326+93C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748736 | ||||||
| chr14:70748809
|
G | GT | 46 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(43): Show | 49 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(46): Show |
intron_variant | MODIFIER | c.1326+19dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748809 | ||||||
| chr14:70749012
|
G | A | 104 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(101): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
splice_region_variant&intron_variant | LOW | c.1151-8C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 4/11 | chr14 | 70749012 | ||||||
| chr14:70749050
|
C | G | 1 | a0001c0006t0017g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1151-46G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 4/11 | chr14 | 70749050 | ||||||
| chr14:70749105
|
T | C | 53 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0002t0001g0004others(50): Show | 57 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1151-101A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 4/11 | chr14 | 70749105 | ||||||
| chr14:70749386
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1151-382A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 4/11 | chr14 | 70749386 | ||||||
| chr14:70750146
|
C | CAT | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1002-66_1002-65ins others(2): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750146 | ||||||
| chr14:70750296
|
C | T | 147 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(144): Show | 155 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1002-215G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750296 | ||||||
| chr14:70750357
|
C | G | 5 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-276G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750357 | ||||||
| chr14:70750502
|
T | C | 102 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(99): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1002-421A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750502 | ||||||
| chr14:70750504
|
G | T | 147 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(144): Show | 155 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1002-423C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750504 | ||||||
| chr14:70750541
|
G | A | 1 | a0001c0001t0004g0341 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1002-460C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750541 | ||||||
| chr14:70750546
|
G | A | 1 | a0001c0021t0071g0143 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1002-465C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750546 | ||||||
| chr14:70750633
|
C | T | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002-552G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750633 | ||||||
| chr14:70750669
|
G | C | 3 | a0001c0002t0020g0003a0001c0002t0020g0013a0001c0002t0038g0012 | 4 | NA18967.hp1 NA18972.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1002-588C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750669 | ||||||
| chr14:70750717
|
C | T | 1 | a0001c0005t0098g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1002-636G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750717 | ||||||
| chr14:70750731
|
C | T | 2 | a0001c0001t0005g0312a0001c0001t0037g0311 | 2 | NA18971.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1002-650G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750731 | ||||||
| chr14:70750911
|
A | T | 147 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(144): Show | 155 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1002-830T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750911 | ||||||
| chr14:70750996
|
A | T | 5 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-915T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750996 | ||||||
| chr14:70751027
|
C | T | 2 | a0002c0008t0003g0216a0002c0008t0003g0218 | 2 | NA18964.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1002-946G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751027 | ||||||
| chr14:70751035
|
C | T | 2 | a0001c0002t0023g0073a0001c0018t0083g0228 | 2 | HG00609.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1002-954G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751035 | ||||||
| chr14:70751059
|
C | CTCTA | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1002-982_1002-979d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751059 | ||||||
| chr14:70751135
|
T | C | 12 | a0001c0002t0001g0066a0001c0002t0001g0113a0001c0002t0008g0114others(9): Show | 12 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1002-1054A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751135 | ||||||
| chr14:70751293
|
A | G | 1 | a0001c0001t0006g0144 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1002-1212T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751293 | ||||||
| chr14:70751348
|
T | A | 1 | a0001c0001t0012g0020 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1002-1267A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751348 | ||||||
| chr14:70751404
|
T | G | 55 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(52): Show | 58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1002-1323A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751404 | ||||||
| chr14:70751425
|
G | A | 1 | a0001c0001t0005g0315 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1002-1344C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751425 | ||||||
| chr14:70751460
|
C | T | 4 | a0001c0003t0001g0083a0001c0003t0008g0170a0001c0003t0008g0179others(1): Show | 4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002-1379G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751460 | ||||||
| chr14:70751462
|
G | A | 5 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-1381C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751462 | ||||||
| chr14:70751466
|
A | T | 4 | a0001c0003t0001g0083a0001c0003t0008g0170a0001c0003t0008g0179others(1): Show | 4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002-1385T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751466 | ||||||
| chr14:70751514
|
T | C | 1 | a0001c0005t0098g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1002-1433A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751514 | ||||||
| chr14:70751724
|
A | T | 1 | a0001c0002t0001g0072 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1002-1643T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751724 | ||||||
| chr14:70751971
|
T | C | 1 | a0001c0001t0012g0032 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1002-1890A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751971 | ||||||
| chr14:70752219
|
T | A | 189 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(186): Show | 200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1002-2138A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752219 | ||||||
| chr14:70752285
|
G | A | 1 | a0001c0002t0016g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1002-2204C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752285 | ||||||
| chr14:70752371
|
T | C | 192 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(189): Show | 203 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1002-2290A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752371 | ||||||
| chr14:70752427
|
C | A | 1 | a0001c0021t0071g0143 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1002-2346G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752427 | ||||||
| chr14:70752447
|
A | G | 2 | a0001c0001t0026g0201a0001c0001t0026g0223 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1002-2366T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752447 | ||||||
| chr14:70752457
|
C | G | 4 | a0001c0002t0022g0022a0001c0002t0022g0023a0001c0002t0059g0024others(1): Show | 4 | HG02723.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1002-2376G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752457 | ||||||
| chr14:70752493
|
G | A | 75 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(72): Show | 78 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1002-2412C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752493 | ||||||
| chr14:70752792
|
T | C | 1 | a0001c0001t0054g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1002-2711A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752792 | ||||||
| chr14:70752846
|
G | A | 4 | a0001c0003t0001g0083a0001c0003t0008g0170a0001c0003t0008g0179others(1): Show | 4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002-2765C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752846 | ||||||
| chr14:70752860
|
C | T | 2 | a0001c0001t0003g0203a0001c0005t0098g0320 | 2 | HG01069.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1002-2779G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752860 | ||||||
| chr14:70753036
|
C | T | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1002-2955G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753036 | ||||||
| chr14:70753116
|
C | G | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1002-3035G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753116 | ||||||
| chr14:70753154
|
C | T | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1002-3073G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753154 | ||||||
| chr14:70753242
|
G | C | 5 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-3161C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753242 | ||||||
| chr14:70753320
|
G | A | 179 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(176): Show | 190 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1002-3239C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753320 | ||||||
| chr14:70753380
|
T | G | 1 | a0011c0010t0003g0209 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1002-3299A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753380 | ||||||
| chr14:70753499
|
G | A | 187 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(184): Show | 198 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1002-3418C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753499 | ||||||
| chr14:70753634
|
C | T | 1 | a0001c0001t0003g0219 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1002-3553G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753634 | ||||||
| chr14:70753636
|
C | T | 1 | a0001c0001t0006g0148 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1002-3555G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753636 | ||||||
| chr14:70753782
|
C | T | 4 | a0001c0002t0022g0022a0001c0002t0022g0023a0001c0002t0059g0024others(1): Show | 4 | HG02723.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1002-3701G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753782 | ||||||
| chr14:70753862
|
A | G | 174 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(171): Show | 185 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1002-3781T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753862 | ||||||
| chr14:70753906
|
T | C | 193 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(190): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1002-3825A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753906 | ||||||
| chr14:70754137
|
T | C | 1 | a0001c0001t0054g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1002-4056A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754137 | ||||||
| chr14:70754145
|
A | G | 1 | a0001c0001t0009g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1002-4064T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754145 | ||||||
| chr14:70754183
|
C | G | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1002-4102G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754183 | ||||||
| chr14:70754378
|
C | T | 1 | a0001c0003t0049g0087 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1002-4297G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754378 | ||||||
| chr14:70754421
|
A | G | 1 | a0001c0002t0016g0091 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1002-4340T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754421 | ||||||
| chr14:70754479
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1002-4398T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754479 | ||||||
| chr14:70754533
|
G | C | 1 | a0001c0001t0011g0009 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1002-4452C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754533 | ||||||
| chr14:70754534
|
C | T | 49 | a0001c0001t0052g0173a0001c0002t0001g0004a0001c0002t0001g0007others(46): Show | 53 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1002-4453G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754534 | ||||||
| chr14:70754565
|
G | A | 1 | a0001c0001t0007g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1002-4484C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754565 | ||||||
| chr14:70754609
|
C | CT | 5 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-4529dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754609 | ||||||
| chr14:70754760
|
C | T | 2 | a0001c0003t0109g0327a0012c0022t0094g0259 | 2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1002-4679G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754760 | ||||||
| chr14:70754806
|
C | A | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1002-4725G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754806 | ||||||
| chr14:70754895
|
C | T | 1 | a0001c0001t0024g0142 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1002-4814G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754895 | ||||||
| chr14:70754972
|
A | G | 5 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-4891T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754972 | ||||||
| chr14:70755011
|
A | T | 1 | a0001c0003t0001g0070 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1002-4930T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755011 | ||||||
| chr14:70755140
|
G | T | 1 | a0001c0001t0007g0279 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1002-5059C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755140 | ||||||
| chr14:70755300
|
G | A | 2 | a0001c0001t0011g0010a0001c0001t0011g0308 | 3 | HG01123.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1002-5219C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755300 | ||||||
| chr14:70755348
|
G | A | 283 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(280): Show | 297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.1002-5267C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755348 | ||||||
| chr14:70755722
|
T | C | 1 | a0001c0002t0022g0023 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1001+5280A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755722 | ||||||
| chr14:70755726
|
T | C | 13 | a0001c0001t0077g0183a0001c0001t0078g0182a0001c0001t0114g0321others(10): Show | 13 | HG00099.hp2 HG00609.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1001+5276A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755726 | ||||||
| chr14:70755727
|
G | A | 5 | a0001c0001t0077g0183a0001c0001t0078g0182a0001c0018t0083g0228others(2): Show | 5 | HG00609.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1001+5275C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755727 | ||||||
| chr14:70755746
|
G | C | 1 | a0001c0011t0051g0184 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1001+5256C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755746 | ||||||
| chr14:70755795
|
T | C | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1001+5207A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755795 | ||||||
| chr14:70755873
|
G | T | 1 | a0001c0002t0061g0095 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1001+5129C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755873 | ||||||
| chr14:70755888
|
C | T | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1001+5114G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755888 | ||||||
| chr14:70756035
|
T | C | 1 | a0001c0002t0001g0072 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1001+4967A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70756035 | ||||||
| chr14:70756271
|
G | A | 1 | a0001c0011t0051g0184 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1001+4731C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70756271 | ||||||
| chr14:70756345
|
C | A | 1 | a0001c0001t0005g0302 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1001+4657G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70756345 | ||||||
| chr14:70756388
|
A | C | 1 | a0001c0001t0003g0198 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1001+4614T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70756388 | ||||||
| chr14:70756480
|
T | A | 11 | a0001c0001t0007g0266a0001c0001t0007g0270a0001c0001t0007g0274others(8): Show | 11 | HG00733.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1001+4522A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70756480 | ||||||
| chr14:70756551
|
C | A | 1 | a0001c0001t0112g0325 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1001+4451G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70756551 | ||||||
| chr14:70757098
|
C | CA | 5 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001+3903dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757098 | ||||||
| chr14:70757387
|
G | A | 1 | a0001c0001t0030g0167 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1001+3615C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757387 | ||||||
| chr14:70757438
|
G | A | 4 | a0001c0001t0007g0274a0001c0001t0007g0285a0001c0001t0028g0244others(1): Show | 4 | HG00733.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1001+3564C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757438 | ||||||
| chr14:70757456
|
G | GA | 7 | a0001c0001t0004g0342a0001c0001t0004g0354a0001c0001t0005g0296others(4): Show | 7 | HG02135.hp2 HG03669.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.1001+3545dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757456 | ||||||
| chr14:70757456
|
GA | G | 190 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(187): Show | 201 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1001+3545delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757456 | ||||||
| chr14:70757503
|
T | C | 192 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(189): Show | 203 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1001+3499A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757503 | ||||||
| chr14:70757525
|
C | A | 1 | a0001c0003t0056g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1001+3477G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757525 | ||||||
| chr14:70757606
|
C | T | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+3396G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757606 | ||||||
| chr14:70757808
|
G | A | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1001+3194C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757808 | ||||||
| chr14:70757834
|
T | A | 1 | a0001c0002t0050g0068 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1001+3168A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757834 | ||||||
| chr14:70757979
|
A | G | 5 | a0001c0003t0001g0069a0001c0003t0001g0070a0001c0003t0001g0077others(2): Show | 5 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001+3023T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757979 | ||||||
| chr14:70757982
|
A | G | 1 | a0001c0003t0001g0069 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1001+3020T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757982 | ||||||
| chr14:70758015
|
A | T | 1 | a0001c0003t0001g0083 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1001+2987T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758015 | ||||||
| chr14:70758073
|
C | T | 5 | a0001c0001t0111g0280a0001c0004t0007g0276a0001c0004t0007g0277others(2): Show | 5 | HG01884.hp1 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1001+2929G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758073 | ||||||
| chr14:70758282
|
G | C | 5 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001+2720C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758282 | ||||||
| chr14:70758319
|
T | C | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1001+2683A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758319 | ||||||
| chr14:70758381
|
T | A | 5 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001+2621A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758381 | ||||||
| chr14:70758382
|
T | A | 182 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(179): Show | 193 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1001+2620A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758382 | ||||||
| chr14:70758383
|
A | T | 27 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0147others(24): Show | 27 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1001+2619T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758383 | ||||||
| chr14:70758394
|
A | G | 1 | a0001c0003t0001g0083 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1001+2608T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758394 | ||||||
| chr14:70758440
|
T | C | 3 | a0001c0002t0001g0075a0001c0002t0008g0080a0001c0002t0062g0079 | 3 | NA18986.hp1 NA19000.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1001+2562A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758440 | ||||||
| chr14:70758448
|
G | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1001+2554C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758448 | ||||||
| chr14:70758577
|
G | A | 5 | a0001c0001t0114g0321a0001c0005t0005g0323a0001c0005t0005g0324others(2): Show | 5 | HG02572.hp1 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001+2425C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758577 | ||||||
| chr14:70758590
|
C | T | 1 | a0001c0001t0004g0330 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1001+2412G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758590 | ||||||
| chr14:70758674
|
A | G | 1 | a0001c0002t0050g0068 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1001+2328T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758674 | ||||||
| chr14:70758756
|
C | G | 6 | a0001c0001t0012g0020a0001c0001t0012g0030a0001c0001t0012g0031others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001+2246G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758756 | ||||||
| chr14:70758928
|
A | C | 1 | a0001c0002t0029g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1001+2074T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758928 | ||||||
| chr14:70759085
|
T | C | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+1917A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759085 | ||||||
| chr14:70759350
|
G | A | 1 | a0001c0021t0071g0143 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1001+1652C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759350 | ||||||
| chr14:70759381
|
G | A | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1001+1621C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759381 | ||||||
| chr14:70759544
|
T | C | 3 | a0001c0001t0004g0337a0001c0001t0004g0338a0001c0001t0004g0339 | 3 | NA18963.hp2 NA18971.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1001+1458A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759544 | ||||||
| chr14:70759586
|
G | C | 99 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(96): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1001+1416C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759586 | ||||||
| chr14:70759842
|
C | T | 20 | a0001c0002t0001g0066a0001c0002t0001g0113a0001c0002t0008g0114others(17): Show | 21 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1001+1160G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759842 | ||||||
| chr14:70759863
|
T | C | 1 | a0001c0002t0023g0074 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1001+1139A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759863 | ||||||
| chr14:70759881
|
C | T | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1001+1121G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759881 | ||||||
| chr14:70760053
|
GC | G | 121 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(118): Show | 128 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1001+948delG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760053 | ||||||
| chr14:70760078
|
CA | C | 4 | a0001c0001t0058g0134a0001c0001t0112g0325a0001c0003t0109g0327others(1): Show | 4 | HG01106.hp2 HG02055.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+923delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760078 | ||||||
| chr14:70760094
|
C | T | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1001+908G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760094 | ||||||
| chr14:70760095
|
G | A | 1 | a0001c0002t0008g0114 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1001+907C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760095 | ||||||
| chr14:70760141
|
G | GCA | 18 | a0001c0001t0004g0337a0001c0001t0004g0338a0001c0001t0004g0339others(15): Show | 19 | HG00733.hp1 HG01123.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.1001+859_1001+860d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760141 | ||||||
| chr14:70760141
|
G | GCACA | 58 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(55): Show | 62 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1001+857_1001+860d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760141 | ||||||
| chr14:70760141
|
G | GCACACA | 64 | a0001c0001t0002g0065a0001c0001t0004g0272a0001c0001t0004g0305others(61): Show | 65 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1001+855_1001+860d others(8): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760141 | ||||||
| chr14:70760141
|
G | GCACACAC others(1): Show |
65 | a0001c0001t0002g0049a0001c0001t0005g0300a0001c0001t0005g0301others(62): Show | 69 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1001+853_1001+860d others(10): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760141 | ||||||
| chr14:70760141
|
G | GCACACAC others(3): Show |
9 | a0001c0001t0027g0246a0001c0001t0111g0280a0001c0002t0001g0082others(6): Show | 9 | HG01361.hp2 HG02080.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1001+851_1001+860d others(12): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760141 | ||||||
| chr14:70760141
|
G | GCACACAC others(5): Show |
3 | a0001c0002t0001g0111a0001c0002t0008g0118a0001c0006t0017g0140 | 3 | HG02809.hp1 HG04204.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1001+849_1001+860d others(14): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760141 | ||||||
| chr14:70760141
|
GCACACAC others(1): Show |
G | 79 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(76): Show | 83 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.1001+853_1001+860d others(10): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760141 | ||||||
| chr14:70760170
|
CACAT | C | 3 | a0001c0001t0074g0188a0001c0001t0076g0187a0001c0001t0115g0319 | 3 | HG01192.hp1 HG02280.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1001+828_1001+831d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760170 | ||||||
| chr14:70760174
|
T | C | 100 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(97): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1001+828A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760174 | ||||||
| chr14:70760306
|
T | C | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+696A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760306 | ||||||
| chr14:70760323
|
G | A | 1 | a0001c0001t0011g0293 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1001+679C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760323 | ||||||
| chr14:70760560
|
A | G | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1001+442T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760560 | ||||||
| chr14:70760825
|
G | A | 1 | a0001c0001t0114g0321 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1001+177C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760825 | ||||||
| chr14:70761196
|
A | C | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.821-14T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761196 | ||||||
| chr14:70761283
|
G | A | 104 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(101): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.821-101C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761283 | ||||||
| chr14:70761320
|
C | A | 1 | a0001c0002t0001g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.821-138G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761320 | ||||||
| chr14:70761491
|
A | T | 5 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-309T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761491 | ||||||
| chr14:70761534
|
G | A | 6 | a0001c0001t0012g0020a0001c0001t0012g0030a0001c0001t0012g0031others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.821-352C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761534 | ||||||
| chr14:70761606
|
T | C | 11 | a0001c0001t0007g0266a0001c0001t0007g0270a0001c0001t0007g0274others(8): Show | 11 | HG00733.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.821-424A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761606 | ||||||
| chr14:70761672
|
G | A | 4 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0029others(1): Show | 4 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-490C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761672 | ||||||
| chr14:70761745
|
T | C | 12 | a0001c0002t0001g0066a0001c0002t0001g0113a0001c0002t0008g0114others(9): Show | 12 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.821-563A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761745 | ||||||
| chr14:70761816
|
T | C | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-634A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761816 | ||||||
| chr14:70761951
|
TG | T | 9 | a0001c0001t0077g0183a0001c0001t0078g0182a0001c0001t0114g0321others(6): Show | 9 | HG02145.hp2 HG02572.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.821-770delC | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761951 | ||||||
| chr14:70761984
|
A | C | 107 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(104): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.821-802T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761984 | ||||||
| chr14:70762065
|
T | C | 4 | a0001c0001t0114g0321a0001c0005t0005g0323a0001c0005t0005g0324others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-883A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70762065 | ||||||
| chr14:70762275
|
C | T | 20 | a0001c0002t0001g0066a0001c0002t0001g0113a0001c0002t0008g0114others(17): Show | 21 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.821-1093G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70762275 | ||||||
| chr14:70762521
|
G | A | 102 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(99): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.821-1339C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70762521 | ||||||
| chr14:70762564
|
C | G | 192 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(189): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.821-1382G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70762564 | ||||||
| chr14:70762730
|
A | G | 10 | a0001c0002t0001g0007a0001c0002t0001g0103a0001c0002t0001g0104others(7): Show | 11 | HG00639.hp1 HG01070.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.821-1548T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70762730 | ||||||
| chr14:70762769
|
T | G | 102 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(99): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.821-1587A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70762769 | ||||||
| chr14:70762995
|
CACAA | C | 56 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(53): Show | 59 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.821-1817_821-1814d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70762995 | ||||||
| chr14:70763172
|
A | C | 1 | a0001c0001t0011g0009 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.821-1990T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763172 | ||||||
| chr14:70763254
|
C | T | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-2072G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763254 | ||||||
| chr14:70763264
|
C | T | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.821-2082G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763264 | ||||||
| chr14:70763265
|
C | T | 1 | a0001c0001t0007g0285 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.821-2083G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763265 | ||||||
| chr14:70763341
|
T | C | 1 | a0001c0001t0004g0342 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.821-2159A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763341 | ||||||
| chr14:70763386
|
C | T | 1 | a0001c0001t0105g0260 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.821-2204G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763386 | ||||||
| chr14:70763422
|
A | G | 1 | a0001c0005t0098g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.821-2240T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763422 | ||||||
| chr14:70763483
|
A | ATAATACC others(1): Show |
189 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(186): Show | 200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.821-2309_821-2302d others(10): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763483 | ||||||
| chr14:70763507
|
C | T | 4 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184others(1): Show | 4 | HG00099.hp2 HG00609.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-2325G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763507 | ||||||
| chr14:70763534
|
CT | C | 190 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(187): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.821-2353delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763534 | ||||||
| chr14:70763591
|
T | C | 5 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-2409A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763591 | ||||||
| chr14:70763615
|
C | T | 6 | a0001c0001t0012g0020a0001c0001t0012g0030a0001c0001t0012g0031others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.821-2433G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763615 | ||||||
| chr14:70763780
|
C | T | 5 | a0001c0001t0005g0300a0001c0001t0005g0301a0001c0001t0005g0306others(2): Show | 5 | NA18612.hp1 NA18948.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.821-2598G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763780 | ||||||
| chr14:70763952
|
G | A | 1 | a0001c0002t0001g0004 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.821-2770C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763952 | ||||||
| chr14:70763981
|
C | T | 3 | a0001c0001t0015g0131a0001c0001t0015g0133a0001c0001t0057g0132 | 3 | HG01433.hp2 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.821-2799G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763981 | ||||||
| chr14:70764012
|
C | T | 1 | a0001c0001t0004g0343 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.821-2830G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764012 | ||||||
| chr14:70764027
|
T | C | 57 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(54): Show | 60 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.821-2845A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764027 | ||||||
| chr14:70764042
|
T | C | 193 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(190): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.821-2860A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764042 | ||||||
| chr14:70764058
|
C | T | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.821-2876G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764058 | ||||||
| chr14:70764067
|
A | T | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.821-2885T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764067 | ||||||
| chr14:70764086
|
T | C | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-2904A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764086 | ||||||
| chr14:70764172
|
G | A | 1 | a0001c0011t0051g0184 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.821-2990C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764172 | ||||||
| chr14:70764187
|
C | T | 34 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0002t0001g0004others(31): Show | 37 | HG00099.hp1 HG00621.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.821-3005G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764187 | ||||||
| chr14:70764192
|
C | CAAAAAAA | 34 | a0001c0001t0002g0001a0001c0001t0002g0036a0001c0001t0002g0037others(31): Show | 37 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.821-3017_821-3011d others(9): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | ||||||
| chr14:70764192
|
C | CAAAAAAA others(3): Show |
1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-3020_821-3011d others(12): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | ||||||
| chr14:70764192
|
C | CAAAAAAA others(4): Show |
4 | a0001c0002t0001g0072a0001c0002t0001g0119a0001c0002t0008g0171others(1): Show | 4 | HG01993.hp1 NA19003.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-3021_821-3011d others(13): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | ||||||
| chr14:70764192
|
C | CAAAAAAA others(5): Show |
46 | a0001c0001t0004g0287a0001c0001t0005g0278a0001c0001t0026g0223others(43): Show | 50 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.821-3022_821-3011d others(14): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | ||||||
| chr14:70764192
|
C | CAAAAAAA others(6): Show |
157 | a0001c0001t0002g0026a0001c0001t0002g0028a0001c0001t0002g0029others(154): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.821-3023_821-3011d others(15): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | ||||||
| chr14:70764192
|
C | CAAAAAAA others(7): Show |
38 | a0001c0001t0002g0027a0001c0001t0003g0195a0001c0001t0003g0198others(35): Show | 38 | HG00735.hp1 HG01106.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.821-3024_821-3011d others(16): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | ||||||
| chr14:70764192
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0074g0188a0001c0001t0075g0189a0001c0003t0008g0179 | 3 | HG02451.hp1 HG03654.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.821-3025_821-3011d others(17): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | ||||||
| chr14:70764192
|
C | CAAAAAAA others(9): Show |
8 | a0001c0001t0006g0157a0001c0001t0006g0161a0001c0001t0030g0167others(5): Show | 8 | HG01109.hp2 HG01496.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.821-3026_821-3011d others(18): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | ||||||
| chr14:70764192
|
C | CAAAAAAA others(10): Show |
11 | a0001c0001t0006g0147a0001c0001t0006g0148a0001c0001t0006g0156others(8): Show | 11 | HG00280.hp1 HG01256.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.821-3027_821-3011d others(19): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | ||||||
| chr14:70764192
|
C | CAAAAAAA others(11): Show |
7 | a0001c0001t0006g0152a0001c0001t0006g0153a0001c0001t0006g0154others(4): Show | 7 | HG02004.hp1 HG02273.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.821-3011_821-3010i others(20): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | ||||||
| chr14:70764192
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0006g0155 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.821-3011_821-3010i others(21): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | ||||||
| chr14:70764192
|
CAAAA | C | 9 | a0001c0001t0077g0183a0001c0001t0078g0182a0001c0001t0114g0321others(6): Show | 9 | HG02145.hp2 HG02572.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.821-3014_821-3011d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | ||||||
| chr14:70764224
|
G | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-3042C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764224 | ||||||
| chr14:70764315
|
A | T | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.821-3133T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764315 | ||||||
| chr14:70764346
|
T | TATTG | 193 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(190): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.821-3165_821-3164i others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764346 | ||||||
| chr14:70764449
|
T | TA | 107 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(104): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.821-3268dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764449 | ||||||
| chr14:70764467
|
C | T | 122 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(119): Show | 129 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.821-3285G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764467 | ||||||
| chr14:70764469
|
G | T | 107 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(104): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.821-3287C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764469 | ||||||
| chr14:70764482
|
G | C | 2 | a0001c0002t0001g0096a0001c0002t0001g0097 | 2 | NA18947.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.821-3300C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764482 | ||||||
| chr14:70764549
|
G | T | 1 | a0001c0001t0004g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.821-3367C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764549 | ||||||
| chr14:70764786
|
T | C | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.821-3604A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764786 | ||||||
| chr14:70764808
|
G | A | 1 | a0001c0001t0005g0301 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.821-3626C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764808 | ||||||
| chr14:70764868
|
T | C | 12 | a0001c0001t0077g0183a0001c0001t0078g0182a0001c0001t0112g0325others(9): Show | 12 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.821-3686A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764868 | ||||||
| chr14:70764869
|
A | G | 1 | a0001c0001t0002g0052 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.821-3687T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764869 | ||||||
| chr14:70764870
|
G | T | 1 | a0001c0001t0002g0052 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.821-3688C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764870 | ||||||
| chr14:70764882
|
T | C | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.821-3700A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764882 | ||||||
| chr14:70764996
|
A | G | 56 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(53): Show | 59 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.821-3814T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764996 | ||||||
| chr14:70765015
|
A | T | 104 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(101): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.821-3833T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765015 | ||||||
| chr14:70765381
|
A | G | 4 | a0001c0004t0007g0276a0001c0004t0007g0277a0001c0004t0028g0243others(1): Show | 4 | HG01884.hp1 HG03195.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-4199T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765381 | ||||||
| chr14:70765430
|
C | T | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.821-4248G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765430 | ||||||
| chr14:70765510
|
A | T | 1 | a0001c0001t0002g0052 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.821-4328T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765510 | ||||||
| chr14:70765511
|
T | A | 1 | a0001c0001t0002g0052 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.821-4329A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765511 | ||||||
| chr14:70765615
|
C | T | 1 | a0001c0002t0063g0115 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.821-4433G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765615 | ||||||
| chr14:70765623
|
C | T | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.821-4441G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765623 | ||||||
| chr14:70765650
|
C | T | 92 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(89): Show | 95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.821-4468G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765650 | ||||||
| chr14:70765672
|
G | A | 1 | a0001c0001t0112g0325 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.821-4490C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765672 | ||||||
| chr14:70765687
|
T | C | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.821-4505A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765687 | ||||||
| chr14:70765689
|
T | C | 3 | a0001c0006t0017g0140a0001c0006t0017g0141a0001c0006t0017g0165 | 3 | HG01884.hp2 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.821-4507A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765689 | ||||||
| chr14:70765735
|
TA | T | 232 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(229): Show | 243 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.821-4554delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765735 | ||||||
| chr14:70765736
|
AAAAAAAA others(18): Show |
A | 11 | a0001c0002t0001g0066a0001c0002t0001g0113a0001c0002t0008g0114others(8): Show | 11 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.821-4579_821-4555d others(27): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765736 | ||||||
| chr14:70765737
|
AAAAAAAA others(17): Show |
A | 1 | a0001c0003t0049g0087 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.821-4579_821-4556d others(26): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765737 | ||||||
| chr14:70765745
|
AAAAAACA others(9): Show |
A | 3 | a0001c0001t0007g0266a0001c0001t0007g0283a0001c0001t0007g0295 | 3 | HG02895.hp1 HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.821-4579_821-4564d others(18): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765745 | ||||||
| chr14:70765746
|
AAAAACAA others(8): Show |
A | 85 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.821-4579_821-4565d others(17): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765746 | ||||||
| chr14:70765747
|
AAAACAAA others(7): Show |
A | 19 | a0001c0001t0012g0020a0001c0001t0012g0030a0001c0001t0012g0031others(16): Show | 19 | HG01192.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.821-4579_821-4566d others(16): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765747 | ||||||
| chr14:70765751
|
C | A | 1 | a0012c0022t0094g0259 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.821-4569G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765751 | ||||||
| chr14:70765754
|
A | C | 180 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(177): Show | 191 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.821-4572T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765754 | ||||||
| chr14:70765761
|
CA | C | 172 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(169): Show | 183 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.821-4580delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765761 | ||||||
| chr14:70765763
|
A | C | 5 | a0001c0001t0089g0256a0001c0004t0007g0276a0001c0004t0007g0277others(2): Show | 5 | HG01884.hp1 HG03195.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-4581T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765763 | ||||||
| chr14:70765764
|
A | C | 102 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(99): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.821-4582T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765764 | ||||||
| chr14:70765774
|
A | C | 1 | a0001c0002t0029g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.821-4592T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765774 | ||||||
| chr14:70765802
|
C | T | 1 | a0001c0001t0081g0210 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.821-4620G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765802 | ||||||
| chr14:70765866
|
A | G | 119 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(116): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.821-4684T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765866 | ||||||
| chr14:70765868
|
G | A | 1 | a0001c0002t0029g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.821-4686C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765868 | ||||||
| chr14:70765979
|
G | A | 1 | a0001c0001t0003g0213 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.821-4797C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765979 | ||||||
| chr14:70766008
|
T | C | 4 | a0001c0003t0001g0083a0001c0003t0008g0170a0001c0003t0008g0179others(1): Show | 4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-4826A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70766008 | ||||||
| chr14:70766199
|
C | T | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.821-5017G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70766199 | ||||||
| chr14:70766316
|
T | C | 1 | a0001c0001t0003g0214 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.821-5134A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70766316 | ||||||
| chr14:70766540
|
C | T | 1 | a0001c0001t0015g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.821-5358G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70766540 | ||||||
| chr14:70766577
|
C | T | 2 | a0001c0001t0002g0038a0001c0001t0002g0041 | 2 | NA18955.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.821-5395G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70766577 | ||||||
| chr14:70766777
|
G | A | 1 | a0001c0001t0007g0274 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.821-5595C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70766777 | ||||||
| chr14:70766941
|
C | T | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.821-5759G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70766941 | ||||||
| chr14:70767099
|
C | G | 189 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(186): Show | 200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.821-5917G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767099 | ||||||
| chr14:70767117
|
C | T | 1 | a0001c0002t0001g0103 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.821-5935G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767117 | ||||||
| chr14:70767279
|
A | G | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.821-6097T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767279 | ||||||
| chr14:70767383
|
CAA | C | 18 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(15): Show | 18 | HG01993.hp1 HG02015.hp1 HG02738.hp1 others(15): Show |
intron_variant | MODIFIER | c.821-6203_821-6202d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767383 | ||||||
| chr14:70767383
|
CAAA | C | 272 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(269): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.821-6204_821-6202d others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767383 | ||||||
| chr14:70767383
|
CAAAA | C | 9 | a0001c0001t0005g0278a0001c0001t0005g0317a0001c0001t0009g0288others(6): Show | 9 | HG00099.hp2 HG01167.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.821-6205_821-6202d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767383 | ||||||
| chr14:70767411
|
C | T | 1 | a0001c0002t0001g0004 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.821-6229G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767411 | ||||||
| chr14:70767653
|
C | T | 1 | a0001c0003t0001g0083 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.821-6471G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767653 | ||||||
| chr14:70767661
|
C | T | 86 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(83): Show | 89 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.821-6479G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767661 | ||||||
| chr14:70767662
|
G | A | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.821-6480C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767662 | ||||||
| chr14:70767678
|
G | A | 14 | a0001c0001t0009g0263a0001c0001t0009g0265a0001c0001t0009g0273others(11): Show | 14 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.821-6496C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767678 | ||||||
| chr14:70767769
|
AC | A | 5 | a0001c0001t0005g0300a0001c0001t0005g0301a0001c0001t0005g0306others(2): Show | 5 | NA18612.hp1 NA18948.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.821-6588delG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767769 | ||||||
| chr14:70767813
|
G | A | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.821-6631C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767813 | ||||||
| chr14:70767876
|
C | T | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-6694G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767876 | ||||||
| chr14:70767879
|
T | C | 189 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(186): Show | 200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.821-6697A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767879 | ||||||
| chr14:70767891
|
G | A | 3 | a0001c0002t0001g0007a0001c0002t0001g0103a0001c0002t0001g0110 | 4 | HG01255.hp1 HG01361.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-6709C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767891 | ||||||
| chr14:70767947
|
T | C | 57 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(54): Show | 60 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.821-6765A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767947 | ||||||
| chr14:70767961
|
T | C | 40 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(37): Show | 40 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.821-6779A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767961 | ||||||
| chr14:70768084
|
T | C | 4 | a0001c0002t0022g0022a0001c0002t0022g0023a0001c0002t0059g0024others(1): Show | 4 | HG02723.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-6902A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768084 | ||||||
| chr14:70768164
|
G | A | 2 | a0001c0001t0076g0187a0001c0001t0115g0319 | 2 | HG01192.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.821-6982C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768164 | ||||||
| chr14:70768287
|
C | A | 3 | a0001c0001t0004g0337a0001c0001t0004g0338a0001c0001t0004g0339 | 3 | NA18963.hp2 NA18971.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.821-7105G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768287 | ||||||
| chr14:70768384
|
T | C | 2 | a0001c0001t0005g0316a0001c0001t0089g0256 | 2 | NA19000.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.821-7202A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768384 | ||||||
| chr14:70768764
|
T | C | 1 | a0001c0001t0002g0064 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.821-7582A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768764 | ||||||
| chr14:70768933
|
T | C | 3 | a0001c0001t0019g0357a0001c0001t0019g0358a0001c0001t0019g0360 | 3 | NA18941.hp1 NA18998.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.821-7751A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768933 | ||||||
| chr14:70768936
|
C | T | 182 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(179): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.821-7754G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768936 | ||||||
| chr14:70768937
|
G | A | 6 | a0001c0001t0012g0020a0001c0001t0012g0030a0001c0001t0012g0031others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.821-7755C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768937 | ||||||
| chr14:70768941
|
C | T | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.821-7759G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768941 | ||||||
| chr14:70769066
|
C | G | 180 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(177): Show | 191 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.821-7884G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769066 | ||||||
| chr14:70769155
|
AC | A | 181 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(178): Show | 192 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.821-7974delG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769155 | ||||||
| chr14:70769284
|
C | T | 2 | a0001c0002t0001g0105a0001c0002t0001g0106 | 2 | HG00639.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.821-8102G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769284 | ||||||
| chr14:70769286
|
G | A | 56 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(53): Show | 59 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.821-8104C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769286 | ||||||
| chr14:70769406
|
T | C | 1 | a0001c0001t0030g0167 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.821-8224A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769406 | ||||||
| chr14:70769537
|
G | T | 4 | a0001c0003t0001g0083a0001c0003t0008g0170a0001c0003t0008g0179others(1): Show | 4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-8355C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769537 | ||||||
| chr14:70769618
|
G | A | 7 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0147others(4): Show | 7 | HG00280.hp1 HG01515.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.821-8436C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769618 | ||||||
| chr14:70769682
|
C | A | 3 | a0001c0002t0001g0096a0001c0002t0001g0097a0001c0002t0061g0095 | 3 | NA18943.hp1 NA18947.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.821-8500G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769682 | ||||||
| chr14:70769804
|
G | A | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-8622C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769804 | ||||||
| chr14:70769933
|
G | C | 4 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(1): Show | 4 | HG02717.hp2 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-8751C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769933 | ||||||
| chr14:70770011
|
C | A | 176 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(173): Show | 187 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.821-8829G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770011 | ||||||
| chr14:70770158
|
G | A | 1 | a0001c0005t0098g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.821-8976C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770158 | ||||||
| chr14:70770180
|
C | T | 98 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(95): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.821-8998G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770180 | ||||||
| chr14:70770283
|
C | T | 2 | a0001c0002t0022g0084a0001c0018t0083g0228 | 2 | HG00609.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.821-9101G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770283 | ||||||
| chr14:70770286
|
T | C | 1 | a0001c0001t0006g0160 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.821-9104A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770286 | ||||||
| chr14:70770297
|
C | T | 1 | a0001c0001t0005g0306 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.821-9115G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770297 | ||||||
| chr14:70770650
|
G | T | 5 | a0001c0001t0003g0194a0001c0001t0026g0201a0001c0001t0026g0220others(2): Show | 5 | HG01256.hp2 HG01258.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-9468C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770650 | ||||||
| chr14:70770833
|
C | T | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-9651G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770833 | ||||||
| chr14:70770844
|
C | G | 2 | a0001c0001t0002g0037a0001c0001t0002g0040 | 2 | NA18960.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.821-9662G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770844 | ||||||
| chr14:70770972
|
T | C | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-9790A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770972 | ||||||
| chr14:70771015
|
T | C | 1 | a0001c0001t0079g0192 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.821-9833A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771015 | ||||||
| chr14:70771050
|
C | CT | 6 | a0001c0001t0077g0183a0001c0001t0078g0182a0001c0002t0016g0089others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.821-9869dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771050 | ||||||
| chr14:70771050
|
C | T | 4 | a0001c0001t0114g0321a0001c0005t0005g0323a0001c0005t0005g0324others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-9868G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771050 | ||||||
| chr14:70771067
|
C | T | 1 | a0001c0001t0004g0272 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.821-9885G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771067 | ||||||
| chr14:70771106
|
G | A | 92 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(89): Show | 95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.821-9924C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771106 | ||||||
| chr14:70771193
|
G | A | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.821-10011C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771193 | ||||||
| chr14:70771348
|
C | T | 3 | a0001c0005t0005g0323a0001c0005t0005g0324a0001c0005t0036g0322 | 3 | HG02572.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.821-10166G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771348 | ||||||
| chr14:70771349
|
C | T | 9 | a0001c0001t0077g0183a0001c0001t0078g0182a0001c0001t0114g0321others(6): Show | 9 | HG02145.hp2 HG02572.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.821-10167G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771349 | ||||||
| chr14:70771428
|
T | C | 1 | a0001c0001t0002g0049 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.821-10246A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771428 | ||||||
| chr14:70771446
|
C | G | 6 | a0001c0001t0003g0002a0001c0001t0003g0195a0001c0001t0003g0196others(3): Show | 8 | NA18940.hp2 NA18947.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.821-10264G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771446 | ||||||
| chr14:70771485
|
C | T | 1 | a0001c0001t0005g0296 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.821-10303G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771485 | ||||||
| chr14:70771581
|
G | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-10399C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771581 | ||||||
| chr14:70771625
|
T | G | 4 | a0001c0003t0001g0083a0001c0003t0008g0170a0001c0003t0008g0179others(1): Show | 4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-10443A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771625 | ||||||
| chr14:70771726
|
T | C | 57 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(54): Show | 60 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.821-10544A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771726 | ||||||
| chr14:70771780
|
A | C | 1 | a0001c0003t0109g0327 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.821-10598T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771780 | ||||||
| chr14:70771818
|
G | A | 1 | a0001c0002t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.821-10636C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771818 | ||||||
| chr14:70771887
|
T | G | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.821-10705A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771887 | ||||||
| chr14:70771897
|
CCTGTTGT others(1): Show |
C | 11 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0234others(8): Show | 11 | NA18949.hp2 NA18964.hp1 NA18968.hp2 others(8): Show |
intron_variant | MODIFIER | c.821-10723_821-1071 others(12): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771897 | ||||||
| chr14:70771969
|
C | T | 180 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(177): Show | 191 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.821-10787G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771969 | ||||||
| chr14:70772041
|
A | G | 1 | a0001c0001t0024g0142 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.821-10859T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772041 | ||||||
| chr14:70772181
|
A | G | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.821-10999T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772181 | ||||||
| chr14:70772195
|
G | A | 1 | a0001c0001t0006g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.821-11013C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772195 | ||||||
| chr14:70772197
|
G | A | 2 | a0001c0001t0004g0353a0001c0001t0004g0354 | 2 | NA19009.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.821-11015C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772197 | ||||||
| chr14:70772250
|
G | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-11068C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772250 | ||||||
| chr14:70772501
|
C | T | 1 | a0001c0001t0012g0020 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.821-11319G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772501 | ||||||
| chr14:70772544
|
G | C | 1 | a0001c0001t0106g0261 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.821-11362C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772544 | ||||||
| chr14:70772688
|
C | T | 1 | a0001c0002t0043g0017 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.821-11506G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772688 | ||||||
| chr14:70772733
|
C | T | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.821-11551G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772733 | ||||||
| chr14:70773052
|
C | T | 1 | a0011c0010t0003g0209 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.821-11870G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773052 | ||||||
| chr14:70773148
|
A | G | 1 | a0001c0001t0009g0288 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.821-11966T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773148 | ||||||
| chr14:70773167
|
G | A | 1 | a0001c0001t0003g0215 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.821-11985C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773167 | ||||||
| chr14:70773171
|
T | C | 2 | a0002c0008t0003g0216a0002c0008t0003g0218 | 2 | NA18964.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.821-11989A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773171 | ||||||
| chr14:70773210
|
A | G | 1 | a0001c0021t0071g0143 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.821-12028T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773210 | ||||||
| chr14:70773364
|
T | C | 1 | a0001c0002t0001g0071 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.821-12182A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773364 | ||||||
| chr14:70773432
|
C | G | 1 | a0011c0010t0003g0209 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.821-12250G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773432 | ||||||
| chr14:70773513
|
C | A | 1 | a0001c0009t0033g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.821-12331G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773513 | ||||||
| chr14:70773600
|
T | C | 1 | a0001c0002t0029g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.821-12418A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773600 | ||||||
| chr14:70773975
|
C | A | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-12793G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773975 | ||||||
| chr14:70774091
|
C | G | 179 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(176): Show | 190 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.821-12909G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774091 | ||||||
| chr14:70774288
|
A | G | 1 | a0001c0002t0016g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.821-13106T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774288 | ||||||
| chr14:70774319
|
T | C | 2 | a0001c0003t0109g0327a0012c0022t0094g0259 | 2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.821-13137A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774319 | ||||||
| chr14:70774403
|
C | T | 1 | a0001c0001t0003g0198 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.821-13221G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774403 | ||||||
| chr14:70774643
|
T | C | 1 | a0001c0001t0005g0297 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.821-13461A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774643 | ||||||
| chr14:70774664
|
A | G | 1 | a0001c0001t0012g0030 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.821-13482T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774664 | ||||||
| chr14:70774725
|
G | A | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-13543C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774725 | ||||||
| chr14:70774726
|
C | G | 1 | a0001c0001t0015g0137 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.821-13544G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774726 | ||||||
| chr14:70774853
|
C | T | 3 | a0001c0001t0007g0266a0001c0001t0007g0283a0001c0001t0007g0295 | 3 | HG02895.hp1 HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.821-13671G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774853 | ||||||
| chr14:70774897
|
T | C | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-13715A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774897 | ||||||
| chr14:70774943
|
C | T | 1 | a0001c0001t0004g0338 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.821-13761G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774943 | ||||||
| chr14:70774946
|
T | C | 4 | a0001c0001t0004g0344a0001c0001t0004g0345a0001c0001t0004g0346others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-13764A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774946 | ||||||
| chr14:70774949
|
A | C | 195 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(192): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.821-13767T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774949 | ||||||
| chr14:70774974
|
C | T | 1 | a0001c0001t0007g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.821-13792G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774974 | ||||||
| chr14:70774983
|
C | CA | 12 | a0001c0001t0004g0331a0001c0001t0004g0335a0001c0001t0004g0336others(9): Show | 12 | HG00621.hp2 HG00673.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.821-13802dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
C | CAAAAAAA others(2): Show |
14 | a0001c0001t0002g0026a0001c0001t0002g0036a0001c0001t0002g0038others(11): Show | 14 | HG00408.hp1 HG02015.hp1 HG03471.hp1 others(11): Show |
intron_variant | MODIFIER | c.821-13810_821-1380 others(13): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
C | CAAAAAAA others(3): Show |
11 | a0001c0001t0002g0037a0001c0001t0002g0050a0001c0001t0002g0055others(8): Show | 11 | HG00597.hp1 HG02056.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.821-13811_821-1380 others(14): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
C | CAAAAAAA others(4): Show |
8 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 11 | NA18945.hp2 NA18953.hp2 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.821-13812_821-1380 others(15): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0002g0054a0001c0001t0021g0051 | 2 | NA18939.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.821-13813_821-1380 others(16): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0002g0028a0001c0001t0002g0041 | 2 | HG02280.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.821-13816_821-1380 others(19): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0002g0029a0001c0001t0025g0025 | 2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.821-13817_821-1380 others(20): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0002g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.821-13818_821-1380 others(21): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
C | CAAAAAAA others(17): Show |
1 | a0001c0003t0001g0083 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.821-13825_821-1380 others(28): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
CA | C | 8 | a0001c0001t0004g0328a0001c0001t0006g0152a0001c0001t0006g0154others(5): Show | 8 | HG02300.hp1 HG03579.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.821-13802delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
CAA | C | 19 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0147others(16): Show | 19 | HG00280.hp1 HG01256.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.821-13803_821-1380 others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
CAAA | C | 38 | a0001c0001t0003g0008a0001c0001t0003g0198a0001c0001t0003g0199others(35): Show | 39 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.821-13804_821-1380 others(7): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
CAAAA | C | 120 | a0001c0001t0003g0002a0001c0001t0003g0194a0001c0001t0003g0195others(117): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.821-13805_821-1380 others(8): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
CAAAAA | C | 22 | a0001c0001t0005g0297a0001c0001t0012g0020a0001c0001t0012g0030others(19): Show | 22 | HG00099.hp2 HG01106.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.821-13806_821-1380 others(9): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
CAAAAAA | C | 9 | a0001c0002t0001g0088a0001c0002t0001g0098a0001c0002t0008g0076others(6): Show | 9 | HG01168.hp1 HG02040.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.821-13807_821-1380 others(10): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
CAAAAAAA | C | 61 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0002t0001g0004others(58): Show | 66 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.821-13808_821-1380 others(11): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0003t0008g0179a0001c0003t0056g0067 | 2 | HG03098.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.821-13813_821-1380 others(16): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70774983
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0003t0008g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.821-13814_821-1380 others(17): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | ||||||
| chr14:70775245
|
T | G | 13 | a0001c0001t0077g0183a0001c0001t0078g0182a0001c0001t0112g0325others(10): Show | 13 | HG01106.hp2 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.821-14063A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70775245 | ||||||
| chr14:70775741
|
G | T | 14 | a0001c0001t0009g0263a0001c0001t0009g0265a0001c0001t0009g0273others(11): Show | 14 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.821-14559C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70775741 | ||||||
| chr14:70775937
|
C | T | 10 | a0001c0001t0007g0266a0001c0001t0007g0270a0001c0001t0007g0274others(7): Show | 10 | HG00733.hp1 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.821-14755G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70775937 | ||||||
| chr14:70775989
|
G | A | 1 | a0001c0011t0051g0184 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.821-14807C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70775989 | ||||||
| chr14:70776047
|
A | T | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-14865T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776047 | ||||||
| chr14:70776065
|
T | C | 53 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0002t0001g0004others(50): Show | 57 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.821-14883A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776065 | ||||||
| chr14:70776158
|
C | T | 4 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0029others(1): Show | 4 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-14976G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776158 | ||||||
| chr14:70776183
|
C | G | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.821-15001G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776183 | ||||||
| chr14:70776285
|
C | T | 1 | a0001c0005t0098g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.821-15103G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776285 | ||||||
| chr14:70776325
|
T | C | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-15143A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776325 | ||||||
| chr14:70776398
|
C | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-15216G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776398 | ||||||
| chr14:70776503
|
T | C | 1 | a0001c0002t0050g0068 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.821-15321A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776503 | ||||||
| chr14:70776626
|
T | A | 55 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(52): Show | 58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.821-15444A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776626 | ||||||
| chr14:70776631
|
G | A | 1 | a0001c0001t0009g0304 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.821-15449C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776631 | ||||||
| chr14:70776707
|
G | A | 2 | a0001c0001t0030g0167a0001c0001t0030g0168 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.821-15525C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776707 | ||||||
| chr14:70776769
|
C | T | 1 | a0001c0001t0005g0307 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.821-15587G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776769 | ||||||
| chr14:70776833
|
CT | C | 289 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(286): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.821-15652delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776833 | ||||||
| chr14:70776900
|
C | A | 3 | a0001c0005t0005g0323a0001c0005t0005g0324a0001c0005t0036g0322 | 3 | HG02572.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.821-15718G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776900 | ||||||
| chr14:70777073
|
T | C | 1 | a0001c0001t0004g0336 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.821-15891A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777073 | ||||||
| chr14:70777111
|
G | A | 1 | a0001c0011t0051g0184 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.821-15929C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777111 | ||||||
| chr14:70777117
|
C | T | 1 | a0001c0002t0008g0080 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.821-15935G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777117 | ||||||
| chr14:70777233
|
C | T | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.821-16051G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777233 | ||||||
| chr14:70777328
|
T | C | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.821-16146A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777328 | ||||||
| chr14:70777358
|
A | G | 1 | a0001c0001t0018g0224 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.821-16176T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777358 | ||||||
| chr14:70777471
|
C | T | 2 | a0001c0001t0026g0220a0001c0001t0080g0221 | 2 | HG01361.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.821-16289G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777471 | ||||||
| chr14:70777476
|
G | A | 1 | a0001c0002t0029g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.821-16294C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777476 | ||||||
| chr14:70777492
|
A | C | 1 | a0001c0001t0002g0060 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.821-16310T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777492 | ||||||
| chr14:70777757
|
C | T | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-16575G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777757 | ||||||
| chr14:70777761
|
C | G | 1 | a0001c0001t0002g0055 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.821-16579G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777761 | ||||||
| chr14:70777794
|
G | A | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-16612C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777794 | ||||||
| chr14:70777808
|
A | C | 1 | a0001c0001t0085g0242 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.821-16626T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777808 | ||||||
| chr14:70778032
|
T | A | 2 | a0001c0001t0009g0263a0001c0001t0009g0273 | 2 | HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.821-16850A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778032 | ||||||
| chr14:70778077
|
T | C | 174 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(171): Show | 185 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.821-16895A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778077 | ||||||
| chr14:70778086
|
T | TTTG | 93 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(90): Show | 96 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.821-16907_821-1690 others(7): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778086 | ||||||
| chr14:70778146
|
A | G | 54 | a0001c0001t0007g0309a0001c0001t0052g0173a0001c0001t0053g0090others(51): Show | 58 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.821-16964T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778146 | ||||||
| chr14:70778276
|
AT | A | 233 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(230): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.821-17095delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778276 | ||||||
| chr14:70778276
|
ATT | A | 11 | a0001c0001t0005g0269a0001c0001t0005g0278a0001c0001t0005g0296others(8): Show | 11 | HG01070.hp2 HG01106.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.821-17096_821-1709 others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778276 | ||||||
| chr14:70778294
|
T | G | 1 | a0001c0001t0003g0219 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.821-17112A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778294 | ||||||
| chr14:70778299
|
C | T | 44 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(41): Show | 47 | HG00408.hp1 HG00597.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.821-17117G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778299 | ||||||
| chr14:70778348
|
C | T | 98 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(95): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.821-17166G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778348 | ||||||
| chr14:70778422
|
T | C | 1 | a0001c0005t0005g0323 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.821-17240A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778422 | ||||||
| chr14:70778457
|
G | A | 178 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(175): Show | 189 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.821-17275C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778457 | ||||||
| chr14:70778477
|
T | C | 5 | a0001c0001t0021g0051a0001c0001t0021g0121a0001c0001t0021g0122others(2): Show | 5 | HG00408.hp1 HG00597.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-17295A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778477 | ||||||
| chr14:70778501
|
C | G | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-17319G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778501 | ||||||
| chr14:70778505
|
A | C | 92 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(89): Show | 95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.821-17323T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778505 | ||||||
| chr14:70778507
|
C | T | 1 | a0001c0001t0004g0351 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.821-17325G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778507 | ||||||
| chr14:70778560
|
G | A | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.821-17378C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778560 | ||||||
| chr14:70778565
|
T | C | 1 | a0001c0011t0051g0184 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.821-17383A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778565 | ||||||
| chr14:70778596
|
A | G | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-17414T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778596 | ||||||
| chr14:70778685
|
C | T | 1 | a0001c0001t0088g0254 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.821-17503G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778685 | ||||||
| chr14:70778731
|
T | C | 4 | a0001c0003t0001g0083a0001c0003t0008g0170a0001c0003t0008g0179others(1): Show | 4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-17549A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778731 | ||||||
| chr14:70778826
|
A | G | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-17644T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778826 | ||||||
| chr14:70778880
|
G | A | 1 | a0001c0009t0033g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.821-17698C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778880 | ||||||
| chr14:70779023
|
GA | G | 184 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(181): Show | 195 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.821-17842delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779023 | ||||||
| chr14:70779115
|
C | T | 5 | a0001c0001t0021g0051a0001c0001t0021g0121a0001c0001t0021g0122others(2): Show | 5 | HG00408.hp1 HG00597.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-17933G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779115 | ||||||
| chr14:70779145
|
A | G | 187 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(184): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.821-17963T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779145 | ||||||
| chr14:70779151
|
G | A | 1 | a0001c0002t0008g0118 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.821-17969C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779151 | ||||||
| chr14:70779165
|
C | T | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.821-17983G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779165 | ||||||
| chr14:70779177
|
C | T | 1 | a0001c0002t0062g0079 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.821-17995G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779177 | ||||||
| chr14:70779234
|
G | A | 4 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(1): Show | 4 | HG02717.hp2 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-18052C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779234 | ||||||
| chr14:70779324
|
A | C | 179 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(176): Show | 190 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.821-18142T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779324 | ||||||
| chr14:70779360
|
C | A | 1 | a0001c0005t0098g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.821-18178G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779360 | ||||||
| chr14:70779480
|
G | T | 1 | a0001c0002t0008g0118 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.821-18298C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779480 | ||||||
| chr14:70779537
|
T | C | 1 | a0001c0002t0001g0075 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.821-18355A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779537 | ||||||
| chr14:70779581
|
C | T | 178 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(175): Show | 189 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.821-18399G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779581 | ||||||
| chr14:70779610
|
T | A | 2 | a0001c0001t0018g0193a0001c0001t0079g0192 | 2 | HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.821-18428A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779610 | ||||||
| chr14:70779669
|
C | T | 184 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(181): Show | 195 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.821-18487G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779669 | ||||||
| chr14:70779945
|
C | T | 2 | a0001c0001t0076g0187a0001c0001t0115g0319 | 2 | HG01192.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.821-18763G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779945 | ||||||
| chr14:70779990
|
G | C | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-18808C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779990 | ||||||
| chr14:70780111
|
A | G | 1 | a0001c0006t0017g0165 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.821-18929T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70780111 | ||||||
| chr14:70780190
|
G | C | 300 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.821-19008C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70780190 | ||||||
| chr14:70780251
|
T | C | 99 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(96): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.821-19069A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70780251 | ||||||
| chr14:70780278
|
T | C | 99 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(96): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.821-19096A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70780278 | ||||||
| chr14:70780322
|
G | A | 1 | a0001c0002t0050g0068 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.821-19140C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70780322 | ||||||
| chr14:70780382
|
T | C | 4 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(1): Show | 4 | HG02717.hp2 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-19200A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70780382 | ||||||
| chr14:70780553
|
T | C | 1 | a0001c0011t0051g0184 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.821-19371A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70780553 | ||||||
| chr14:70781078
|
T | G | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+19589A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781078 | ||||||
| chr14:70781196
|
G | T | 3 | a0001c0001t0004g0337a0001c0001t0004g0338a0001c0001t0004g0339 | 3 | NA18963.hp2 NA18971.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.820+19471C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781196 | ||||||
| chr14:70781512
|
T | C | 78 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0001t0055g0085others(75): Show | 83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.820+19155A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781512 | ||||||
| chr14:70781549
|
A | G | 1 | a0001c0005t0098g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.820+19118T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781549 | ||||||
| chr14:70781674
|
T | C | 181 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(178): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.820+18993A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781674 | ||||||
| chr14:70781790
|
T | G | 1 | a0001c0001t0074g0188 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.820+18877A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781790 | ||||||
| chr14:70781873
|
A | C | 2 | a0001c0001t0055g0085a0001c0002t0022g0084 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.820+18794T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781873 | ||||||
| chr14:70781964
|
G | T | 4 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0029others(1): Show | 4 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+18703C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781964 | ||||||
| chr14:70782046
|
C | T | 1 | a0001c0001t0092g0251 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.820+18621G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782046 | ||||||
| chr14:70782312
|
A | G | 2 | a0001c0001t0002g0037a0001c0001t0002g0040 | 2 | NA18960.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.820+18355T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782312 | ||||||
| chr14:70782376
|
A | G | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+18291T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782376 | ||||||
| chr14:70782377
|
T | C | 172 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(169): Show | 182 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.820+18290A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782377 | ||||||
| chr14:70782387
|
T | C | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+18280A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782387 | ||||||
| chr14:70782473
|
C | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.820+18194G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782473 | ||||||
| chr14:70782513
|
C | T | 93 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(90): Show | 96 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.820+18154G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782513 | ||||||
| chr14:70782754
|
C | G | 122 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(119): Show | 128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.820+17913G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782754 | ||||||
| chr14:70782781
|
C | G | 1 | a0001c0001t0103g0262 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.820+17886G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782781 | ||||||
| chr14:70782981
|
G | A | 3 | a0001c0001t0112g0325a0001c0003t0109g0327a0012c0022t0094g0259 | 3 | HG01106.hp2 HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.820+17686C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782981 | ||||||
| chr14:70782999
|
C | T | 1 | a0001c0001t0003g0208 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.820+17668G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782999 | ||||||
| chr14:70783000
|
G | A | 2 | a0001c0001t0002g0064a0001c0001t0004g0348 | 2 | NA19088.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.820+17667C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783000 | ||||||
| chr14:70783085
|
C | T | 26 | a0001c0001t0055g0085a0001c0002t0001g0066a0001c0002t0001g0113others(23): Show | 27 | HG00323.hp1 HG00609.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.820+17582G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783085 | ||||||
| chr14:70783260
|
G | A | 1 | a0001c0001t0014g0127 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.820+17407C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783260 | ||||||
| chr14:70783317
|
T | A | 1 | a0001c0001t0007g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.820+17350A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783317 | ||||||
| chr14:70783360
|
C | T | 1 | a0001c0001t0004g0330 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.820+17307G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783360 | ||||||
| chr14:70783461
|
C | CT | 175 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(172): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.820+17205_820+1720 others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783461 | ||||||
| chr14:70783547
|
C | T | 1 | a0001c0002t0020g0013 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.820+17120G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783547 | ||||||
| chr14:70783560
|
C | T | 4 | a0001c0001t0007g0274a0001c0001t0007g0285a0001c0001t0028g0244others(1): Show | 4 | HG00733.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+17107G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783560 | ||||||
| chr14:70783561
|
G | A | 1 | a0001c0021t0071g0143 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.820+17106C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783561 | ||||||
| chr14:70784031
|
C | T | 1 | a0001c0001t0003g0207 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.820+16636G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784031 | ||||||
| chr14:70784042
|
G | C | 149 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(146): Show | 159 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.820+16625C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784042 | ||||||
| chr14:70784140
|
G | C | 5 | a0001c0001t0111g0280a0001c0004t0007g0276a0001c0004t0007g0277others(2): Show | 5 | HG01884.hp1 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.820+16527C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784140 | ||||||
| chr14:70784247
|
C | G | 26 | a0001c0001t0055g0085a0001c0002t0001g0066a0001c0002t0001g0113others(23): Show | 27 | HG00323.hp1 HG00609.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.820+16420G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784247 | ||||||
| chr14:70784295
|
A | G | 2 | a0001c0001t0003g0206a0008c0016t0003g0205 | 2 | HG01081.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.820+16372T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784295 | ||||||
| chr14:70784311
|
A | T | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+16356T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784311 | ||||||
| chr14:70784323
|
A | T | 79 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0001t0055g0085others(76): Show | 84 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.820+16344T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784323 | ||||||
| chr14:70784466
|
G | A | 99 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(96): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.820+16201C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784466 | ||||||
| chr14:70784485
|
G | A | 55 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(52): Show | 58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.820+16182C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784485 | ||||||
| chr14:70784507
|
C | G | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+16160G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784507 | ||||||
| chr14:70784509
|
G | A | 3 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141 | 3 | HG02717.hp2 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.820+16158C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784509 | ||||||
| chr14:70784616
|
G | A | 1 | a0001c0001t0002g0065 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.820+16051C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784616 | ||||||
| chr14:70784666
|
C | T | 1 | a0001c0006t0017g0165 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.820+16001G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784666 | ||||||
| chr14:70784705
|
G | C | 93 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(90): Show | 96 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.820+15962C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784705 | ||||||
| chr14:70784726
|
A | C | 1 | a0001c0002t0032g0078 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.820+15941T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784726 | ||||||
| chr14:70784749
|
G | C | 38 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(35): Show | 41 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.820+15918C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784749 | ||||||
| chr14:70784769
|
T | C | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.820+15898A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784769 | ||||||
| chr14:70784877
|
A | G | 2 | a0001c0001t0003g0008a0001c0001t0018g0204 | 3 | HG00642.hp1 HG00735.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.820+15790T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784877 | ||||||
| chr14:70784916
|
A | C | 1 | a0001c0001t0009g0263 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.820+15751T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784916 | ||||||
| chr14:70785506
|
T | G | 1 | a0001c0001t0087g0250 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.820+15161A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785506 | ||||||
| chr14:70785576
|
G | A | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+15091C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785576 | ||||||
| chr14:70785655
|
G | A | 1 | a0001c0021t0071g0143 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.820+15012C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785655 | ||||||
| chr14:70785680
|
T | C | 55 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(52): Show | 58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.820+14987A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785680 | ||||||
| chr14:70785694
|
T | C | 6 | a0001c0001t0012g0020a0001c0001t0012g0030a0001c0001t0012g0031others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.820+14973A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785694 | ||||||
| chr14:70785742
|
G | C | 1 | a0001c0002t0001g0088 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.820+14925C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785742 | ||||||
| chr14:70785846
|
C | T | 1 | a0001c0002t0008g0118 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.820+14821G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785846 | ||||||
| chr14:70785901
|
C | T | 55 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(52): Show | 58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.820+14766G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785901 | ||||||
| chr14:70785905
|
A | C | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+14762T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785905 | ||||||
| chr14:70785938
|
G | C | 159 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(156): Show | 169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.820+14729C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785938 | ||||||
| chr14:70786040
|
A | C | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+14627T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786040 | ||||||
| chr14:70786069
|
A | C | 159 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(156): Show | 169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.820+14598T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786069 | ||||||
| chr14:70786070
|
G | A | 106 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(103): Show | 112 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.820+14597C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786070 | ||||||
| chr14:70786105
|
T | C | 1 | a0001c0021t0071g0143 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.820+14562A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786105 | ||||||
| chr14:70786305
|
A | G | 1 | a0001c0001t0006g0156 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.820+14362T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786305 | ||||||
| chr14:70786352
|
C | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(93): Show | 102 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.820+14315G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786352 | ||||||
| chr14:70786486
|
C | T | 2 | a0001c0001t0014g0185a0001c0001t0014g0186 | 2 | HG03654.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.820+14181G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786486 | ||||||
| chr14:70786505
|
A | C | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+14162T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786505 | ||||||
| chr14:70786558
|
G | C | 1 | a0001c0005t0098g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.820+14109C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786558 | ||||||
| chr14:70786784
|
T | C | 76 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(73): Show | 79 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.820+13883A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786784 | ||||||
| chr14:70786794
|
A | G | 1 | a0001c0011t0051g0184 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.820+13873T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786794 | ||||||
| chr14:70786918
|
T | C | 1 | a0001c0001t0075g0189 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.820+13749A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786918 | ||||||
| chr14:70787041
|
A | G | 1 | a0001c0001t0003g0203 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.820+13626T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787041 | ||||||
| chr14:70787042
|
T | C | 1 | a0001c0003t0001g0083 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.820+13625A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787042 | ||||||
| chr14:70787070
|
A | C | 4 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(1): Show | 4 | HG02717.hp2 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+13597T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787070 | ||||||
| chr14:70787226
|
T | C | 1 | a0001c0003t0008g0179 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.820+13441A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787226 | ||||||
| chr14:70787275
|
A | G | 4 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(1): Show | 4 | HG02717.hp2 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+13392T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787275 | ||||||
| chr14:70787336
|
G | A | 1 | a0001c0001t0005g0316 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.820+13331C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787336 | ||||||
| chr14:70787398
|
C | T | 99 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(96): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.820+13269G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787398 | ||||||
| chr14:70787401
|
G | A | 54 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(51): Show | 57 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.820+13266C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787401 | ||||||
| chr14:70787409
|
G | A | 55 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(52): Show | 58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.820+13258C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787409 | ||||||
| chr14:70787451
|
C | G | 1 | a0001c0001t0106g0261 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.820+13216G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787451 | ||||||
| chr14:70787454
|
G | A | 1 | a0001c0001t0002g0040 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.820+13213C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787454 | ||||||
| chr14:70787507
|
C | CA | 37 | a0001c0001t0002g0059a0001c0001t0004g0349a0001c0001t0005g0316others(34): Show | 37 | HG00280.hp1 HG01109.hp2 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.820+13159dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787507 | ||||||
| chr14:70787507
|
CA | C | 134 | a0001c0001t0002g0041a0001c0001t0003g0002a0001c0001t0003g0008others(131): Show | 142 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.820+13159delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787507 | ||||||
| chr14:70787544
|
C | A | 78 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0001t0055g0085others(75): Show | 83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.820+13123G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787544 | ||||||
| chr14:70787777
|
GT | G | 10 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(7): Show | 10 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.820+12889delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787777 | ||||||
| chr14:70787817
|
A | C | 3 | a0001c0001t0013g0035a0001c0001t0013g0043a0001c0001t0013g0044 | 3 | NA18950.hp1 NA18995.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.820+12850T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787817 | ||||||
| chr14:70787947
|
C | T | 4 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(1): Show | 4 | HG02717.hp2 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+12720G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787947 | ||||||
| chr14:70787981
|
C | A | 288 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(285): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.820+12686G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787981 | ||||||
| chr14:70788065
|
A | G | 1 | a0001c0006t0017g0140 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.820+12602T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788065 | ||||||
| chr14:70788217
|
T | C | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.820+12450A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788217 | ||||||
| chr14:70788237
|
C | T | 149 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(146): Show | 159 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.820+12430G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788237 | ||||||
| chr14:70788270
|
A | G | 2 | a0001c0001t0055g0085a0001c0002t0022g0084 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.820+12397T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788270 | ||||||
| chr14:70788395
|
C | A | 1 | a0001c0003t0049g0087 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.820+12272G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788395 | ||||||
| chr14:70788426
|
C | T | 10 | a0001c0001t0007g0266a0001c0001t0007g0270a0001c0001t0007g0274others(7): Show | 10 | HG00733.hp1 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.820+12241G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788426 | ||||||
| chr14:70788527
|
A | G | 1 | a0001c0006t0017g0165 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.820+12140T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788527 | ||||||
| chr14:70788573
|
C | T | 3 | a0001c0001t0034g0129a0001c0001t0034g0130a0001c0001t0069g0128 | 3 | HG02630.hp2 HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.820+12094G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788573 | ||||||
| chr14:70788718
|
A | G | 78 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0001t0055g0085others(75): Show | 83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.820+11949T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788718 | ||||||
| chr14:70788739
|
G | T | 1 | a0001c0003t0056g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.820+11928C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788739 | ||||||
| chr14:70788779
|
G | C | 21 | a0001c0001t0055g0085a0001c0002t0001g0066a0001c0002t0001g0113others(18): Show | 22 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.820+11888C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788779 | ||||||
| chr14:70788859
|
A | T | 1 | a0001c0001t0099g0284 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.820+11808T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788859 | ||||||
| chr14:70789189
|
G | T | 158 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(155): Show | 168 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.820+11478C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789189 | ||||||
| chr14:70789233
|
G | A | 25 | a0001c0001t0055g0085a0001c0002t0001g0066a0001c0002t0001g0113others(22): Show | 26 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.820+11434C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789233 | ||||||
| chr14:70789512
|
C | A | 3 | a0001c0003t0008g0170a0001c0003t0008g0179a0001c0003t0056g0067 | 3 | HG03098.hp1 HG03540.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.820+11155G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789512 | ||||||
| chr14:70789598
|
T | C | 1 | a0001c0002t0001g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.820+11069A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789598 | ||||||
| chr14:70789604
|
G | C | 1 | a0001c0001t0012g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.820+11063C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789604 | ||||||
| chr14:70789608
|
T | C | 1 | a0001c0001t0005g0315 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.820+11059A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789608 | ||||||
| chr14:70789650
|
G | A | 106 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(103): Show | 112 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.820+11017C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789650 | ||||||
| chr14:70789672
|
G | T | 1 | a0001c0002t0008g0076 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.820+10995C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789672 | ||||||
| chr14:70789717
|
G | A | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+10950C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789717 | ||||||
| chr14:70789834
|
T | C | 1 | a0001c0006t0017g0165 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.820+10833A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789834 | ||||||
| chr14:70789912
|
G | A | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+10755C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789912 | ||||||
| chr14:70789944
|
C | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.820+10723G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789944 | ||||||
| chr14:70790007
|
G | A | 1 | a0001c0002t0001g0099 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.820+10660C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790007 | ||||||
| chr14:70790055
|
G | A | 5 | a0001c0001t0003g0194a0001c0001t0026g0201a0001c0001t0026g0220others(2): Show | 5 | HG01256.hp2 HG01258.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+10612C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790055 | ||||||
| chr14:70790085
|
G | A | 1 | a0001c0001t0005g0310 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.820+10582C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790085 | ||||||
| chr14:70790219
|
T | C | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+10448A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790219 | ||||||
| chr14:70790281
|
C | G | 1 | a0001c0001t0039g0014 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.820+10386G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790281 | ||||||
| chr14:70790478
|
G | A | 99 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(96): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.820+10189C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790478 | ||||||
| chr14:70790689
|
A | G | 172 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(169): Show | 182 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.820+9978T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790689 | ||||||
| chr14:70790690
|
T | C | 2 | a0001c0001t0019g0357a0001c0001t0019g0358 | 2 | NA18998.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.820+9977A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790690 | ||||||
| chr14:70790701
|
A | C | 2 | a0001c0001t0006g0154a0001c0001t0006g0155 | 2 | NA18747.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.820+9966T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790701 | ||||||
| chr14:70790869
|
C | A | 1 | a0001c0001t0002g0041 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.820+9798G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790869 | ||||||
| chr14:70790883
|
C | G | 53 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0002t0001g0004others(50): Show | 57 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.820+9784G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790883 | ||||||
| chr14:70791442
|
A | G | 122 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(119): Show | 128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.820+9225T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70791442 | ||||||
| chr14:70791476
|
T | C | 3 | a0001c0001t0004g0344a0001c0001t0004g0345a0001c0001t0004g0346 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.820+9191A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70791476 | ||||||
| chr14:70791588
|
C | T | 1 | a0001c0001t0027g0245 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.820+9079G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70791588 | ||||||
| chr14:70791589
|
G | A | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+9078C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70791589 | ||||||
| chr14:70791683
|
C | T | 1 | a0001c0002t0001g0088 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.820+8984G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70791683 | ||||||
| chr14:70791724
|
C | T | 55 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(52): Show | 58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.820+8943G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70791724 | ||||||
| chr14:70791951
|
G | A | 6 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(3): Show | 6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+8716C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70791951 | ||||||
| chr14:70792577
|
C | T | 1 | a0001c0001t0004g0338 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.820+8090G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70792577 | ||||||
| chr14:70792680
|
C | T | 7 | a0001c0001t0055g0085a0001c0001t0076g0187a0001c0002t0022g0022others(4): Show | 7 | HG01192.hp1 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.820+7987G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70792680 | ||||||
| chr14:70792902
|
G | A | 1 | a0001c0002t0001g0100 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.820+7765C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70792902 | ||||||
| chr14:70792955
|
C | T | 328 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(325): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.820+7712G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70792955 | ||||||
| chr14:70792987
|
G | A | 5 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+7680C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70792987 | ||||||
| chr14:70793111
|
T | C | 1 | a0001c0001t0007g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.820+7556A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793111 | ||||||
| chr14:70793149
|
C | T | 8 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0234others(5): Show | 8 | NA18949.hp2 NA18964.hp1 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.820+7518G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793149 | ||||||
| chr14:70793164
|
G | T | 168 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(165): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.820+7503C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793164 | ||||||
| chr14:70793179
|
T | C | 5 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(2): Show | 5 | HG01192.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+7488A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793179 | ||||||
| chr14:70793374
|
C | T | 168 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(165): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.820+7293G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793374 | ||||||
| chr14:70793536
|
AAAAT | A | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.820+7127_820+7130d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793536 | ||||||
| chr14:70793585
|
A | G | 3 | a0001c0005t0005g0323a0001c0005t0005g0324a0001c0005t0036g0322 | 3 | HG02572.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.820+7082T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793585 | ||||||
| chr14:70793590
|
T | C | 53 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0002t0001g0004others(50): Show | 57 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.820+7077A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793590 | ||||||
| chr14:70793591
|
G | A | 4 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(1): Show | 4 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+7076C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793591 | ||||||
| chr14:70793652
|
T | TTTCA | 220 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0028others(217): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.820+7011_820+7014d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793652 | ||||||
| chr14:70793652
|
T | TTTCATTC others(1): Show |
35 | a0001c0001t0002g0027a0001c0001t0003g0202a0001c0001t0005g0296others(32): Show | 35 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.820+7007_820+7014d others(10): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793652 | ||||||
| chr14:70793652
|
T | TTTCATTC others(5): Show |
1 | a0001c0001t0024g0142 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.820+7003_820+7014d others(14): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793652 | ||||||
| chr14:70793781
|
T | C | 1 | a0001c0001t0003g0226 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.820+6886A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793781 | ||||||
| chr14:70793846
|
G | A | 12 | a0001c0002t0001g0066a0001c0002t0001g0113a0001c0002t0008g0114others(9): Show | 12 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.820+6821C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793846 | ||||||
| chr14:70793912
|
T | C | 4 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141others(1): Show | 4 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+6755A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793912 | ||||||
| chr14:70794038
|
T | C | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.820+6629A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794038 | ||||||
| chr14:70794119
|
G | A | 2 | a0001c0002t0001g0102a0001c0002t0068g0101 | 2 | HG02155.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.820+6548C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794119 | ||||||
| chr14:70794132
|
C | A | 1 | a0001c0001t0005g0302 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.820+6535G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794132 | ||||||
| chr14:70794149
|
G | C | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.820+6518C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794149 | ||||||
| chr14:70794193
|
A | C | 1 | a0001c0001t0006g0153 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.820+6474T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794193 | ||||||
| chr14:70794291
|
G | C | 1 | a0003c0007t0096g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.820+6376C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794291 | ||||||
| chr14:70794295
|
T | C | 21 | a0001c0001t0005g0264a0001c0001t0005g0269a0001c0001t0005g0278others(18): Show | 21 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.820+6372A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794295 | ||||||
| chr14:70794308
|
G | C | 1 | a0001c0001t0003g0222 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.820+6359C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794308 | ||||||
| chr14:70794325
|
T | C | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.820+6342A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794325 | ||||||
| chr14:70794420
|
T | A | 2 | a0001c0001t0034g0130a0001c0001t0069g0128 | 2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.820+6247A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794420 | ||||||
| chr14:70794591
|
TA | T | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+6075delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794591 | ||||||
| chr14:70794660
|
G | A | 3 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188 | 3 | HG02486.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.820+6007C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794660 | ||||||
| chr14:70794693
|
T | TC | 93 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(90): Show | 96 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.820+5973dupG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794693 | ||||||
| chr14:70794747
|
G | A | 36 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0147others(33): Show | 36 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.820+5920C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794747 | ||||||
| chr14:70794913
|
G | A | 328 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(325): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.820+5754C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794913 | ||||||
| chr14:70794935
|
C | T | 78 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0001t0055g0085others(75): Show | 83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.820+5732G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794935 | ||||||
| chr14:70794938
|
A | G | 1 | a0001c0001t0002g0036 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.820+5729T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794938 | ||||||
| chr14:70794966
|
C | T | 1 | a0001c0001t0005g0278 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.820+5701G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794966 | ||||||
| chr14:70794967
|
G | A | 1 | a0001c0001t0018g0224 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.820+5700C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794967 | ||||||
| chr14:70794989
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0085g0242 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.820+5677_820+5678i others(14): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794989 | ||||||
| chr14:70794990
|
C | CT | 66 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(63): Show | 69 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.820+5676dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | ||||||
| chr14:70794990
|
C | CTTT | 33 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(30): Show | 36 | HG00408.hp1 HG02015.hp1 HG02056.hp2 others(33): Show |
intron_variant | MODIFIER | c.820+5674_820+5676d others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | ||||||
| chr14:70794990
|
C | CTTTT | 6 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0059others(3): Show | 6 | HG00597.hp1 HG00609.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+5673_820+5676d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | ||||||
| chr14:70794990
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0005g0303a0001c0001t0005g0307a0001c0001t0009g0304 | 3 | HG00323.hp2 NA18946.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.820+5667_820+5676d others(12): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | ||||||
| chr14:70794990
|
C | CTTTTTTT others(4): Show |
53 | a0001c0001t0004g0287a0001c0001t0005g0011a0001c0001t0005g0264others(50): Show | 56 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.820+5666_820+5676d others(13): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | ||||||
| chr14:70794990
|
C | CTTTTTTT others(5): Show |
36 | a0001c0001t0004g0272a0001c0001t0005g0278a0001c0001t0005g0306others(33): Show | 36 | HG00438.hp2 HG00597.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.820+5665_820+5676d others(14): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | ||||||
| chr14:70794990
|
C | CTTTTTTT others(6): Show |
6 | a0001c0001t0007g0270a0001c0001t0012g0031a0001c0001t0088g0254others(3): Show | 6 | HG01891.hp1 HG02074.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.820+5664_820+5676d others(15): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | ||||||
| chr14:70794990
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0012g0032a0001c0001t0112g0325 | 2 | HG01106.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.820+5663_820+5676d others(16): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | ||||||
| chr14:70794990
|
C | T | 1 | a0001c0001t0085g0242 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.820+5677G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | ||||||
| chr14:70795031
|
T | C | 78 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0001t0055g0085others(75): Show | 83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.820+5636A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795031 | ||||||
| chr14:70795037
|
G | A | 55 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(52): Show | 58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.820+5630C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795037 | ||||||
| chr14:70795075
|
C | T | 1 | a0001c0002t0001g0071 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.820+5592G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795075 | ||||||
| chr14:70795137
|
G | A | 1 | a0001c0001t0005g0306 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.820+5530C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795137 | ||||||
| chr14:70795164
|
T | G | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+5503A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795164 | ||||||
| chr14:70795187
|
G | A | 1 | a0001c0001t0012g0031 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.820+5480C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795187 | ||||||
| chr14:70795310
|
A | C | 4 | a0001c0004t0007g0276a0001c0004t0007g0277a0001c0004t0028g0243others(1): Show | 4 | HG01884.hp1 HG03195.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+5357T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795310 | ||||||
| chr14:70795348
|
G | A | 2 | a0001c0001t0074g0188a0001c0011t0051g0184 | 2 | NA20129.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.820+5319C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795348 | ||||||
| chr14:70795411
|
C | T | 27 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0147others(24): Show | 27 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.820+5256G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795411 | ||||||
| chr14:70795505
|
T | C | 55 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(52): Show | 58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.820+5162A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795505 | ||||||
| chr14:70795578
|
C | T | 1 | a0001c0003t0008g0179 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.820+5089G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795578 | ||||||
| chr14:70795620
|
C | T | 96 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(93): Show | 99 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.820+5047G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795620 | ||||||
| chr14:70795767
|
C | CT | 100 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(97): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.820+4899dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795767 | ||||||
| chr14:70795852
|
G | A | 1 | a0001c0009t0033g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.820+4815C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795852 | ||||||
| chr14:70796142
|
T | TC | 140 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(137): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.820+4524dupG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796142 | ||||||
| chr14:70796215
|
T | C | 140 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(137): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.820+4452A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796215 | ||||||
| chr14:70796277
|
G | A | 53 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0002t0001g0004others(50): Show | 57 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.820+4390C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796277 | ||||||
| chr14:70796348
|
T | C | 1 | a0001c0006t0017g0165 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.820+4319A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796348 | ||||||
| chr14:70796420
|
T | C | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.820+4247A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796420 | ||||||
| chr14:70796452
|
T | C | 1 | a0001c0021t0071g0143 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.820+4215A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796452 | ||||||
| chr14:70796481
|
G | A | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+4186C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796481 | ||||||
| chr14:70796485
|
C | A | 1 | a0001c0001t0030g0168 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.820+4182G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796485 | ||||||
| chr14:70796519
|
C | G | 96 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(93): Show | 99 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.820+4148G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796519 | ||||||
| chr14:70796555
|
G | A | 5 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+4112C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796555 | ||||||
| chr14:70796578
|
T | C | 1 | a0001c0002t0023g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.820+4089A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796578 | ||||||
| chr14:70796606
|
G | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.820+4061C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796606 | ||||||
| chr14:70796710
|
C | T | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.820+3957G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796710 | ||||||
| chr14:70796721
|
C | T | 5 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(2): Show | 5 | HG01192.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+3946G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796721 | ||||||
| chr14:70796795
|
G | A | 1 | a0001c0009t0033g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.820+3872C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796795 | ||||||
| chr14:70796926
|
A | C | 1 | a0001c0003t0001g0083 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.820+3741T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796926 | ||||||
| chr14:70797136
|
C | T | 27 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0147others(24): Show | 27 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.820+3531G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797136 | ||||||
| chr14:70797233
|
C | A | 1 | a0001c0001t0002g0049 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.820+3434G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797233 | ||||||
| chr14:70797260
|
C | T | 3 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141 | 3 | HG02717.hp2 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.820+3407G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797260 | ||||||
| chr14:70797341
|
A | G | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+3326T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797341 | ||||||
| chr14:70797389
|
C | T | 74 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0001t0055g0085others(71): Show | 79 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.820+3278G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797389 | ||||||
| chr14:70797404
|
C | T | 4 | a0001c0003t0001g0083a0001c0003t0008g0170a0001c0003t0008g0179others(1): Show | 4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+3263G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797404 | ||||||
| chr14:70797407
|
A | G | 140 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(137): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.820+3260T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797407 | ||||||
| chr14:70797417
|
A | AAAT | 137 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(134): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.820+3247_820+3249d others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797417 | ||||||
| chr14:70797442
|
A | C | 1 | a0001c0002t0008g0076 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.820+3225T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797442 | ||||||
| chr14:70797536
|
G | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.820+3131C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797536 | ||||||
| chr14:70797638
|
C | T | 1 | a0001c0006t0017g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.820+3029G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797638 | ||||||
| chr14:70797891
|
A | C | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+2776T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797891 | ||||||
| chr14:70797956
|
G | C | 96 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(93): Show | 99 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.820+2711C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797956 | ||||||
| chr14:70798165
|
C | G | 1 | a0001c0001t0006g0151 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.820+2502G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798165 | ||||||
| chr14:70798194
|
A | C | 1 | a0001c0011t0051g0184 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.820+2473T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798194 | ||||||
| chr14:70798201
|
A | G | 79 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0001t0055g0085others(76): Show | 84 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.820+2466T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798201 | ||||||
| chr14:70798313
|
G | A | 1 | a0001c0002t0029g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.820+2354C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798313 | ||||||
| chr14:70798425
|
T | TATCTGCT others(20): Show |
218 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(215): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.820+2241_820+2242i others(29): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798425 | ||||||
| chr14:70798425
|
T | TTTTCCAG others(33): Show |
1 | a0001c0002t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.820+2241_820+2242i others(42): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798425 | ||||||
| chr14:70798435
|
C | G | 2 | a0001c0003t0008g0170a0001c0003t0008g0179 | 2 | HG03540.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.820+2232G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798435 | ||||||
| chr14:70798461
|
G | A | 1 | a0001c0003t0008g0179 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.820+2206C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798461 | ||||||
| chr14:70798471
|
G | GT | 54 | a0001c0001t0002g0041a0001c0001t0004g0272a0001c0001t0004g0331others(51): Show | 55 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.820+2195dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | ||||||
| chr14:70798471
|
G | GTT | 27 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(24): Show | 30 | HG00408.hp1 HG01192.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.820+2194_820+2195d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | ||||||
| chr14:70798471
|
G | GTTT | 19 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(16): Show | 19 | HG00597.hp1 HG01109.hp2 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.820+2193_820+2195d others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | ||||||
| chr14:70798471
|
G | GTTTT | 25 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0147others(22): Show | 25 | HG00280.hp1 HG01515.hp1 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.820+2192_820+2195d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | ||||||
| chr14:70798471
|
G | GTTTTTT | 10 | a0001c0001t0015g0133a0001c0001t0015g0137a0001c0001t0026g0223others(7): Show | 10 | HG01074.hp1 HG01081.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.820+2190_820+2195d others(8): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | ||||||
| chr14:70798471
|
G | GTTTTTTT | 33 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(30): Show | 36 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.820+2189_820+2195d others(9): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | ||||||
| chr14:70798471
|
G | GTTTTTTT others(1): Show |
11 | a0001c0001t0003g0195a0001c0001t0003g0196a0001c0001t0003g0197others(8): Show | 11 | HG01258.hp2 HG01346.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.820+2188_820+2195d others(10): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | ||||||
| chr14:70798471
|
GT | G | 8 | a0001c0001t0004g0329a0001c0001t0005g0307a0001c0001t0007g0318others(5): Show | 8 | HG00609.hp1 HG01496.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.820+2195delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | ||||||
| chr14:70798501
|
C | T | 1 | a0001c0002t0001g0075 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.820+2166G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798501 | ||||||
| chr14:70798536
|
T | C | 96 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(93): Show | 99 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.820+2131A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798536 | ||||||
| chr14:70798603
|
C | T | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+2064G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798603 | ||||||
| chr14:70798639
|
CG | C | 7 | a0001c0001t0005g0011a0001c0001t0005g0312a0001c0001t0005g0313others(4): Show | 8 | HG03654.hp2 NA18945.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.820+2027delC | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798639 | ||||||
| chr14:70798695
|
G | T | 18 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(15): Show | 21 | HG00408.hp1 HG00597.hp1 NA18939.hp1 others(18): Show |
intron_variant | MODIFIER | c.820+1972C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798695 | ||||||
| chr14:70798699
|
C | T | 1 | a0001c0001t0003g0194 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.820+1968G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798699 | ||||||
| chr14:70798783
|
G | C | 5 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(2): Show | 5 | HG01192.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+1884C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798783 | ||||||
| chr14:70798911
|
C | T | 5 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(2): Show | 5 | HG01192.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+1756G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798911 | ||||||
| chr14:70799056
|
C | T | 36 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0147others(33): Show | 36 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.820+1611G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799056 | ||||||
| chr14:70799080
|
A | G | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.820+1587T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799080 | ||||||
| chr14:70799101
|
A | G | 55 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(52): Show | 58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.820+1566T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799101 | ||||||
| chr14:70799132
|
C | G | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.820+1535G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799132 | ||||||
| chr14:70799176
|
AT | A | 53 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(50): Show | 56 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.820+1490delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799176 | ||||||
| chr14:70799204
|
T | C | 10 | a0001c0002t0001g0007a0001c0002t0001g0103a0001c0002t0001g0104others(7): Show | 11 | HG00639.hp1 HG01070.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.820+1463A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799204 | ||||||
| chr14:70799233
|
G | A | 1 | a0001c0002t0001g0111 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.820+1434C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799233 | ||||||
| chr14:70799251
|
G | C | 359 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(356): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.820+1416C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799251 | ||||||
| chr14:70799310
|
A | G | 359 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(356): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.820+1357T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799310 | ||||||
| chr14:70799346
|
G | T | 36 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0147others(33): Show | 36 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.820+1321C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799346 | ||||||
| chr14:70799408
|
C | T | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.820+1259G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799408 | ||||||
| chr14:70799433
|
G | A | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.820+1234C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799433 | ||||||
| chr14:70799501
|
G | A | 1 | a0001c0001t0075g0189 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.820+1166C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799501 | ||||||
| chr14:70799540
|
C | T | 1 | a0001c0001t0006g0151 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.820+1127G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799540 | ||||||
| chr14:70799628
|
C | T | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.820+1039G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799628 | ||||||
| chr14:70799631
|
G | A | 60 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(57): Show | 63 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.820+1036C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799631 | ||||||
| chr14:70799726
|
G | A | 7 | a0001c0002t0001g0066a0001c0002t0001g0113a0001c0002t0008g0114others(4): Show | 7 | HG01255.hp2 HG02155.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.820+941C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799726 | ||||||
| chr14:70799999
|
CATTTAAT | C | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.820+661_820+667del others(7): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799999 | ||||||
| chr14:70800062
|
A | G | 219 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(216): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.820+605T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800062 | ||||||
| chr14:70800205
|
A | G | 100 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(97): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.820+462T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800205 | ||||||
| chr14:70800225
|
C | T | 60 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(57): Show | 63 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.820+442G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800225 | ||||||
| chr14:70800252
|
G | T | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.820+415C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800252 | ||||||
| chr14:70800530
|
C | T | 1 | a0001c0001t0021g0121 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.820+137G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800530 | ||||||
| chr14:70800600
|
C | T | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+67G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800600 | ||||||
| chr14:70800628
|
C | T | 55 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(52): Show | 58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.820+39G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800628 | ||||||
| chr14:70800634
|
T | C | 1 | a0001c0001t0004g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.820+33A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800634 | ||||||
| chr14:70801247
|
TATTTTCC others(5): Show |
T | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.407-179_407-168del others(12): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70801247 | ||||||
| chr14:70801330
|
A | G | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.407-250T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70801330 | ||||||
| chr14:70801382
|
G | A | 2 | a0001c0002t0001g0116a0001c0002t0001g0117 | 2 | HG01106.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.407-302C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70801382 | ||||||
| chr14:70801543
|
C | T | 3 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0066g0146 | 3 | HG02523.hp1 NA18984.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.407-463G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70801543 | ||||||
| chr14:70801729
|
G | C | 48 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(45): Show | 51 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.407-649C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70801729 | ||||||
| chr14:70802157
|
A | G | 1 | a0009c0017t0025g0180 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.407-1077T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802157 | ||||||
| chr14:70802235
|
C | G | 2 | a0001c0001t0072g0191a0001c0001t0073g0190 | 2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.407-1155G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802235 | ||||||
| chr14:70802260
|
G | T | 1 | a0001c0001t0112g0325 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.407-1180C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802260 | ||||||
| chr14:70802394
|
A | G | 219 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(216): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.407-1314T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802394 | ||||||
| chr14:70802415
|
T | C | 1 | a0001c0001t0005g0315 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.407-1335A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802415 | ||||||
| chr14:70802715
|
T | C | 2 | a0001c0001t0004g0349a0001c0001t0004g0350 | 2 | HG00673.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.407-1635A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802715 | ||||||
| chr14:70802847
|
T | A | 3 | a0001c0006t0017g0139a0001c0006t0017g0140a0001c0006t0017g0141 | 3 | HG02717.hp2 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.407-1767A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802847 | ||||||
| chr14:70802852
|
G | C | 2 | a0001c0001t0003g0225a0001c0001t0003g0226 | 2 | HG01515.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.407-1772C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802852 | ||||||
| chr14:70802899
|
A | C | 219 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(216): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.407-1819T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802899 | ||||||
| chr14:70802946
|
G | A | 17 | a0001c0001t0006g0151a0001c0001t0006g0152a0001c0001t0006g0153others(14): Show | 17 | HG01256.hp1 HG01952.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.407-1866C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802946 | ||||||
| chr14:70802978
|
C | T | 60 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(57): Show | 63 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.407-1898G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802978 | ||||||
| chr14:70803044
|
A | G | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.407-1964T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803044 | ||||||
| chr14:70803149
|
T | A | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.407-2069A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803149 | ||||||
| chr14:70803221
|
G | A | 1 | a0001c0001t0007g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.407-2141C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803221 | ||||||
| chr14:70803305
|
A | G | 1 | a0001c0002t0001g0066 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.407-2225T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803305 | ||||||
| chr14:70803336
|
T | TC | 3 | a0001c0001t0024g0169a0001c0001t0030g0167a0001c0001t0030g0168 | 3 | HG03209.hp1 HG03579.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.407-2257_407-2256i others(3): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803336 | ||||||
| chr14:70803337
|
T | A | 4 | a0001c0001t0006g0166a0001c0001t0024g0169a0001c0001t0030g0167others(1): Show | 4 | HG03209.hp1 HG03579.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.407-2257A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | ||||||
| chr14:70803337
|
T | C | 22 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0147others(19): Show | 22 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.407-2257A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | ||||||
| chr14:70803337
|
T | TA | 25 | a0001c0001t0004g0351a0001c0001t0004g0353a0001c0001t0004g0354others(22): Show | 27 | HG00609.hp2 HG00673.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.407-2258dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | ||||||
| chr14:70803337
|
T | TAA | 9 | a0001c0001t0002g0037a0001c0001t0002g0038a0001c0001t0002g0039others(6): Show | 9 | HG02015.hp1 HG02145.hp2 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.407-2259_407-2258d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | ||||||
| chr14:70803337
|
T | TAAA | 33 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(30): Show | 36 | HG00408.hp1 HG00597.hp1 HG02056.hp2 others(33): Show |
intron_variant | MODIFIER | c.407-2260_407-2258d others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | ||||||
| chr14:70803337
|
TA | T | 24 | a0001c0001t0004g0330a0001c0001t0005g0269a0001c0001t0007g0266others(21): Show | 24 | HG01070.hp2 HG01891.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.407-2258delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | ||||||
| chr14:70803337
|
TAA | T | 65 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0001t0055g0085others(62): Show | 70 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.407-2259_407-2258d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | ||||||
| chr14:70803337
|
TAAA | T | 9 | a0001c0002t0001g0066a0001c0002t0001g0071a0001c0002t0001g0072others(6): Show | 9 | HG01167.hp1 HG01168.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.407-2260_407-2258d others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | ||||||
| chr14:70803337
|
TAAAAAA | T | 51 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(48): Show | 54 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.407-2263_407-2258d others(8): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | ||||||
| chr14:70803338
|
A | C | 1 | a0001c0001t0024g0142 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.407-2258T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803338 | ||||||
| chr14:70803349
|
A | C | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | NA18939.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.407-2269T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803349 | ||||||
| chr14:70803614
|
A | G | 1 | a0001c0003t0008g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.407-2534T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803614 | ||||||
| chr14:70803774
|
T | A | 1 | a0001c0009t0033g0124 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.407-2694A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803774 | ||||||
| chr14:70803786
|
C | A | 41 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.407-2706G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803786 | ||||||
| chr14:70803848
|
C | T | 1 | a0001c0001t0009g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.407-2768G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803848 | ||||||
| chr14:70803974
|
G | C | 5 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(2): Show | 5 | HG01192.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.407-2894C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803974 | ||||||
| chr14:70803990
|
T | C | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.407-2910A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803990 | ||||||
| chr14:70804014
|
C | T | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-2934G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804014 | ||||||
| chr14:70804063
|
G | A | 2 | a0001c0002t0001g0119a0001c0002t0008g0118 | 2 | NA19011.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.407-2983C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804063 | ||||||
| chr14:70804151
|
T | C | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.407-3071A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804151 | ||||||
| chr14:70804194
|
C | G | 5 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.407-3114G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804194 | ||||||
| chr14:70804223
|
G | C | 1 | a0001c0001t0007g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.407-3143C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804223 | ||||||
| chr14:70804279
|
A | G | 36 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0147others(33): Show | 36 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.407-3199T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804279 | ||||||
| chr14:70804296
|
A | G | 1 | a0001c0005t0098g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407-3216T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804296 | ||||||
| chr14:70804338
|
T | G | 329 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(326): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.407-3258A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804338 | ||||||
| chr14:70804544
|
C | T | 1 | a0001c0001t0054g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.407-3464G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804544 | ||||||
| chr14:70804632
|
T | C | 78 | a0001c0001t0052g0173a0001c0001t0053g0090a0001c0001t0055g0085others(75): Show | 83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.407-3552A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804632 | ||||||
| chr14:70804659
|
A | G | 55 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(52): Show | 58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.407-3579T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804659 | ||||||
| chr14:70804692
|
TAA | T | 55 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(52): Show | 58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.407-3614_407-3613d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804692 | ||||||
| chr14:70804729
|
A | G | 1 | a0001c0001t0005g0264 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.407-3649T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804729 | ||||||
| chr14:70804731
|
G | A | 1 | a0001c0003t0109g0327 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.407-3651C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804731 | ||||||
| chr14:70804759
|
C | T | 1 | a0001c0001t0009g0263 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.407-3679G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804759 | ||||||
| chr14:70804800
|
A | T | 3 | a0001c0009t0033g0123a0001c0009t0033g0124a0001c0011t0051g0184 | 3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.407-3720T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804800 | ||||||
| chr14:70804823
|
C | T | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-3743G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804823 | ||||||
| chr14:70805275
|
CCTT | C | 4 | a0001c0005t0005g0323a0001c0005t0005g0324a0001c0005t0036g0322others(1): Show | 4 | HG01496.hp2 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+3488_406+3490d others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70805275 | ||||||
| chr14:70805587
|
C | A | 1 | a0001c0001t0005g0317 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.406+3179G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70805587 | ||||||
| chr14:70805906
|
G | A | 1 | a0001c0002t0008g0120 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.406+2860C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70805906 | ||||||
| chr14:70806075
|
G | A | 60 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(57): Show | 63 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.406+2691C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806075 | ||||||
| chr14:70806084
|
A | G | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.406+2682T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806084 | ||||||
| chr14:70806108
|
C | T | 55 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0194others(52): Show | 58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.406+2658G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806108 | ||||||
| chr14:70806146
|
C | T | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.406+2620G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806146 | ||||||
| chr14:70806244
|
T | C | 1 | a0001c0001t0010g0241 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.406+2522A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806244 | ||||||
| chr14:70806458
|
A | G | 4 | a0001c0002t0022g0022a0001c0002t0022g0023a0001c0002t0059g0024others(1): Show | 4 | HG02723.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.406+2308T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806458 | ||||||
| chr14:70806650
|
T | G | 1 | a0001c0001t0085g0242 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.406+2116A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806650 | ||||||
| chr14:70806692
|
T | C | 1 | a0001c0001t0073g0190 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.406+2074A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806692 | ||||||
| chr14:70806710
|
C | G | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+2056G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806710 | ||||||
| chr14:70806742
|
C | T | 6 | a0001c0001t0114g0321a0001c0005t0005g0323a0001c0005t0005g0324others(3): Show | 6 | HG01496.hp2 HG02572.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.406+2024G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806742 | ||||||
| chr14:70806894
|
C | T | 1 | a0001c0001t0115g0319 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.406+1872G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806894 | ||||||
| chr14:70807058
|
T | C | 1 | a0001c0001t0007g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.406+1708A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807058 | ||||||
| chr14:70807155
|
G | A | 1 | a0001c0001t0027g0255 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.406+1611C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807155 | ||||||
| chr14:70807220
|
G | A | 1 | a0001c0018t0083g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.406+1546C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807220 | ||||||
| chr14:70807232
|
C | A | 2 | a0001c0001t0004g0353a0001c0001t0004g0354 | 2 | NA19009.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.406+1534G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807232 | ||||||
| chr14:70807267
|
G | A | 1 | a0001c0001t0115g0319 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.406+1499C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807267 | ||||||
| chr14:70807327
|
T | C | 1 | a0001c0011t0051g0184 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.406+1439A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807327 | ||||||
| chr14:70807363
|
G | A | 1 | a0001c0001t0089g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.406+1403C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807363 | ||||||
| chr14:70807483
|
C | T | 2 | a0001c0009t0033g0123a0001c0009t0033g0124 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.406+1283G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807483 | ||||||
| chr14:70807608
|
T | G | 1 | a0001c0002t0020g0013 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.406+1158A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807608 | ||||||
| chr14:70807862
|
T | A | 92 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(89): Show | 95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.406+904A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807862 | ||||||
| chr14:70807960
|
G | T | 328 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(325): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.406+806C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807960 | ||||||
| chr14:70807972
|
T | G | 4 | a0001c0001t0077g0183a0001c0001t0078g0182a0009c0017t0025g0180others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+794A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807972 | ||||||
| chr14:70808005
|
C | G | 95 | a0001c0001t0004g0272a0001c0001t0004g0287a0001c0001t0004g0305others(92): Show | 98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.406+761G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808005 | ||||||
| chr14:70808013
|
C | T | 1 | a0001c0001t0012g0020 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.406+753G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808013 | ||||||
| chr14:70808157
|
T | C | 2 | a0001c0001t0021g0121a0001c0001t0021g0122 | 2 | HG00408.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.406+609A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808157 | ||||||
| chr14:70808432
|
G | C | 1 | a0001c0001t0082g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.406+334C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808432 | ||||||
| chr14:70808439
|
C | CG | 116 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(113): Show | 124 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.406+326dupC | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808439 | ||||||
| chr14:70808441
|
G | C | 1 | a0001c0001t0009g0355 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.406+325C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808441 | ||||||
| chr14:70808443
|
G | C | 1 | a0001c0011t0051g0184 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.406+323C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808443 | ||||||
| chr14:70808541
|
G | A | 1 | a0001c0001t0113g0356 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.406+225C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808541 | ||||||
| chr14:70808606
|
A | G | 223 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(220): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.406+160T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808606 | ||||||
| chr14:70808662
|
C | A | 5 | a0001c0001t0072g0191a0001c0001t0073g0190a0001c0001t0074g0188others(2): Show | 5 | HG01192.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.406+104G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808662 | ||||||
| chr14:70808758
|
C | A | 1 | a0001c0001t0072g0191 | 1 | HG02486.hp1 | splice_region_variant&intron_variant | LOW | c.406+8G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808758 |