Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5601 |
| ensemblid | ENSG00000050748.18 |
| hgncid | 6886 |
| symbol | MAPK9 |
| name | mitogen-activated protein kinase 9 |
| refseq_nuc | NM_002752.5 |
| refseq_prot | NP_002743.3 |
| ensembl_nuc | ENST00000452135.7 |
| ensembl_prot | ENSP00000394560.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 180233143 |
| end | 180292083 |
| strand | - |
| ver | v1.2 |
| region | chr5:180233143-180292083 |
| region5000 | chr5:180228143-180297083 |
| regionname0 | MAPK9_chr5_180233143_180292083 |
| regionname5000 | MAPK9_chr5_180228143_180297083 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 424 | 371 | 90 | 68 | 151 | 16 | 44 | 109 | MAPK9_chr5_180228143_180297083 | MAPK9 | MSDSK others(419): Show |
chr5 | 180228143 | 180297083 |
| a0002 | 0/0 | 424 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | MSDSK others(419): Show |
chr5 | 180228143 | 180297083 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1272 | 369 | 88 | 68 | 151 | 16 | 44 | MAPK9_chr5_180228143_180297083 | MAPK9 | ATGAG others(1267): Show |
chr5 | 180228143 | 180297083 | ||
| a0001c0002 | 0/0 | 1272 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | ATGAG others(1267): Show |
chr5 | 180228143 | 180297083 | ||
| a0002c0003 | 0/0 | 1272 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | ATGAG others(1267): Show |
chr5 | 180228143 | 180297083 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4796 | 109 | 18 | 13 | 66 | 5 | 7 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0002 | 1/0 | 4799 | 38 | 6 | 3 | 19 | 2 | 7 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4794): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0003 | 0/0 | 4799 | 29 | 5 | 11 | 7 | 3 | 3 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4794): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0004 | 0/0 | 4793 | 24 | 1 | 10 | 9 | 0 | 4 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4788): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0005 | 0/0 | 4793 | 21 | 1 | 0 | 20 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4788): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0006 | 0/0 | 4802 | 18 | 9 | 2 | 7 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4797): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0007 | 0/0 | 4796 | 18 | 0 | 1 | 13 | 1 | 3 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0008 | 0/0 | 4799 | 17 | 2 | 9 | 0 | 3 | 3 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4794): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0009 | 0/0 | 4796 | 13 | 2 | 9 | 0 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0010 | 0/0 | 4799 | 6 | 0 | 1 | 0 | 1 | 4 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4794): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0011 | 0/0 | 4796 | 5 | 2 | 1 | 0 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0012 | 0/0 | 4796 | 3 | 3 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0013 | 0/1 | 4796 | 5 | 1 | 0 | 1 | 1 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0014 | 0/0 | 4793 | 5 | 5 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4788): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0015 | 0/0 | 4802 | 4 | 4 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4797): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0016 | 0/0 | 4799 | 4 | 4 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4794): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0017 | 0/0 | 4796 | 4 | 1 | 1 | 0 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0018 | 0/0 | 4796 | 4 | 0 | 3 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0019 | 0/0 | 4796 | 4 | 4 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0020 | 0/0 | 4796 | 4 | 1 | 0 | 1 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0021 | 0/0 | 4796 | 3 | 2 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0022 | 0/0 | 4796 | 3 | 3 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0023 | 0/0 | 4799 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4794): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0024 | 0/0 | 4796 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0025 | 0/0 | 4796 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0026 | 0/0 | 4793 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4788): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0027 | 0/0 | 4793 | 2 | 1 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4788): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0028 | 0/0 | 4802 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4797): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0029 | 0/0 | 4799 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4794): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0030 | 0/0 | 4799 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4794): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0031 | 0/0 | 4799 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4794): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0032 | 0/0 | 4799 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4794): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0033 | 0/0 | 4799 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4794): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0034 | 0/0 | 4796 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0035 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0036 | 0/0 | 4796 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0037 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0038 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0039 | 0/0 | 4796 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0040 | 0/0 | 4796 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0041 | 0/0 | 4793 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4788): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0042 | 0/0 | 4796 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0043 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0044 | 0/0 | 4799 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4794): Show |
chr5 | 180228143 | 180297083 |
| a0001c0001t0045 | 0/0 | 4796 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0001c0002t0012 | 0/0 | 4796 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4791): Show |
chr5 | 180228143 | 180297083 |
| a0002c0003t0003 | 0/0 | 4799 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | AGACC others(4794): Show |
chr5 | 180228143 | 180297083 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0002 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0010g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0010g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0010g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0010g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0011g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0011g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0011g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0011g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0011g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0012g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0012g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0012g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0013g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0013g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0013g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0013g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0013g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0014g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0014g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0014g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0014g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0014g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0015g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0015g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0015g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0015g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0016g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0016g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0016g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0017g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0017g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0017g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0018g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0018g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0018g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0018g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0019g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0019g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0019g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0019g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0020g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0020g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0020g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0020g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0021g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0021g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0021g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0022g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0022g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0022g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0023g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0023g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0024g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0024g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0025g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0025g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0026g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0026g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0027g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0027g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0028g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0029g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0030g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0031g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0032g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0033g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0034g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0035g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0036g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0037g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0038g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0039g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0040g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0041g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0042g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0043g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0044g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0045g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0002t0012g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0002t0012g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0002c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0007 | EUR | GBR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00099 | hp2 | a0001 | c0001 | t0007 | g0134 | EUR | GBR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | GBR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | GBR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | FIN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0087 | EUR | FIN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0327 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0304 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0290 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00621 | hp2 | a0001 | c0001 | t0035 | g0145 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0326 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00639 | hp2 | a0001 | c0001 | t0010 | g0047 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0324 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00733 | hp2 | a0001 | c0001 | t0008 | g0010 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0075 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01071 | hp1 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01074 | hp2 | a0001 | c0001 | t0009 | g0002 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01099 | hp1 | a0001 | c0001 | t0018 | g0123 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0328 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01106 | hp2 | a0001 | c0001 | t0008 | g0010 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0089 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0331 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01167 | hp2 | a0001 | c0001 | t0006 | g0029 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0076 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01175 | hp2 | a0001 | c0001 | t0009 | g0231 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01192 | hp1 | a0001 | c0001 | t0011 | g0197 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01243 | hp1 | a0001 | c0001 | t0017 | g0155 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0027 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0097 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0325 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01256 | hp1 | a0001 | c0001 | t0034 | g0233 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0099 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0100 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01261 | hp1 | a0001 | c0001 | t0009 | g0018 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01261 | hp2 | a0001 | c0001 | t0008 | g0003 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0329 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01358 | hp1 | a0001 | c0001 | t0008 | g0053 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01358 | hp2 | a0001 | c0001 | t0009 | g0017 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0074 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01496 | hp1 | a0001 | c0001 | t0009 | g0018 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0003 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0096 | EUR | IBS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01515 | hp2 | a0001 | c0001 | t0008 | g0079 | EUR | IBS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01516 | hp1 | a0001 | c0001 | t0008 | g0011 | EUR | IBS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | IBS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0011 | EUR | IBS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0083 | EUR | IBS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0025 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01884 | hp2 | a0001 | c0001 | t0022 | g0343 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01928 | hp2 | a0001 | c0001 | t0018 | g0124 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0313 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01934 | hp2 | a0001 | c0001 | t0033 | g0056 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01952 | hp2 | a0001 | c0001 | t0039 | g0242 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01975 | hp2 | a0001 | c0001 | t0007 | g0013 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0332 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01978 | hp2 | a0001 | c0001 | t0009 | g0266 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01993 | hp1 | a0001 | c0001 | t0009 | g0002 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02004 | hp2 | a0001 | c0001 | t0018 | g0212 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02055 | hp1 | a0001 | c0001 | t0015 | g0023 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02055 | hp2 | a0001 | c0001 | t0028 | g0031 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0038 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0288 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0314 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02080 | hp1 | a0001 | c0001 | t0041 | g0302 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0206 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02145 | hp2 | a0001 | c0001 | t0045 | g0344 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02148 | hp1 | a0001 | c0001 | t0009 | g0234 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02155 | hp2 | a0001 | c0001 | t0007 | g0131 | EAS | CDX | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02165 | hp1 | a0001 | c0001 | t0030 | g0064 | EAS | CDX | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0081 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02258 | hp1 | a0001 | c0001 | t0032 | g0111 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02258 | hp2 | a0001 | c0001 | t0024 | g0261 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02280 | hp1 | a0001 | c0001 | t0025 | g0213 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02280 | hp2 | a0001 | c0001 | t0016 | g0120 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02300 | hp1 | a0001 | c0001 | t0040 | g0208 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02300 | hp2 | a0001 | c0001 | t0009 | g0002 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0033 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02451 | hp2 | a0001 | c0001 | t0014 | g0307 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0296 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02572 | hp1 | a0001 | c0001 | t0020 | g0204 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0098 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02602 | hp2 | a0001 | c0001 | t0009 | g0232 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02615 | hp2 | a0001 | c0001 | t0015 | g0024 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02622 | hp2 | a0001 | c0001 | t0022 | g0342 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02630 | hp2 | a0001 | c0002 | t0012 | g0245 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02647 | hp1 | a0001 | c0001 | t0026 | g0291 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02683 | hp1 | a0001 | c0001 | t0027 | g0334 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02683 | hp2 | a0001 | c0001 | t0009 | g0002 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02698 | hp1 | a0001 | c0001 | t0010 | g0104 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02698 | hp2 | a0001 | c0001 | t0008 | g0072 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02717 | hp2 | a0001 | c0001 | t0019 | g0217 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02738 | hp1 | a0001 | c0001 | t0007 | g0220 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0042 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02895 | hp1 | a0001 | c0001 | t0016 | g0045 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02895 | hp2 | a0001 | c0001 | t0012 | g0240 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02897 | hp1 | a0001 | c0001 | t0012 | g0241 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02922 | hp1 | a0001 | c0001 | t0016 | g0008 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02922 | hp2 | a0001 | c0001 | t0019 | g0215 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02965 | hp1 | a0001 | c0001 | t0023 | g0122 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02976 | hp1 | a0001 | c0001 | t0014 | g0311 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03130 | hp1 | a0001 | c0001 | t0017 | g0154 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03130 | hp2 | a0001 | c0001 | t0014 | g0309 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03139 | hp1 | a0001 | c0001 | t0019 | g0214 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03139 | hp2 | a0001 | c0001 | t0015 | g0022 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03195 | hp1 | a0001 | c0001 | t0013 | g0247 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0034 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03225 | hp1 | a0001 | c0001 | t0024 | g0260 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03239 | hp1 | a0001 | c0001 | t0013 | g0129 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0267 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03490 | hp1 | a0001 | c0001 | t0021 | g0253 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03490 | hp2 | a0001 | c0001 | t0017 | g0014 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0057 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03491 | hp2 | a0001 | c0001 | t0010 | g0012 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03492 | hp1 | a0001 | c0001 | t0017 | g0014 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03492 | hp2 | a0001 | c0001 | t0010 | g0012 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03516 | hp2 | a0001 | c0001 | t0019 | g0216 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0292 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0218 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03579 | hp1 | a0001 | c0001 | t0023 | g0121 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03579 | hp2 | a0001 | c0001 | t0014 | g0308 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0333 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0320 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03688 | hp2 | a0001 | c0001 | t0007 | g0219 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0312 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03710 | hp1 | a0001 | c0001 | t0042 | g0338 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03710 | hp2 | a0001 | c0001 | t0011 | g0198 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03927 | hp2 | a0001 | c0001 | t0008 | g0046 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03942 | hp1 | a0001 | c0001 | t0020 | g0228 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04115 | hp1 | a0001 | c0001 | t0010 | g0107 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0319 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04184 | hp1 | a0001 | c0001 | t0020 | g0229 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04204 | hp2 | a0001 | c0001 | t0036 | g0137 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04228 | hp1 | a0001 | c0001 | t0011 | g0199 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18522 | hp1 | a0001 | c0001 | t0014 | g0310 | AFR | YRI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | YRI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | YRI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18906 | hp2 | a0001 | c0001 | t0022 | g0341 | AFR | YRI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18944 | hp2 | a0001 | c0001 | t0007 | g0013 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18949 | hp1 | a0001 | c0001 | t0043 | g0339 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18949 | hp2 | a0001 | c0001 | t0006 | g0037 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18951 | hp1 | a0002 | c0003 | t0003 | g0102 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18951 | hp2 | a0001 | c0001 | t0037 | g0281 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0289 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18956 | hp1 | a0001 | c0001 | t0006 | g0039 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0297 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18960 | hp1 | a0001 | c0001 | t0006 | g0036 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0294 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0287 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0317 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18964 | hp1 | a0001 | c0001 | t0020 | g0230 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0322 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18966 | hp2 | a0001 | c0001 | t0007 | g0225 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18969 | hp1 | a0001 | c0001 | t0005 | g0299 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18970 | hp1 | a0001 | c0001 | t0007 | g0223 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0336 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18972 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18977 | hp1 | a0001 | c0001 | t0018 | g0211 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0295 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18981 | hp1 | a0001 | c0001 | t0005 | g0301 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18982 | hp2 | a0001 | c0001 | t0007 | g0227 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18991 | hp2 | a0001 | c0001 | t0013 | g0265 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18992 | hp1 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0305 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18995 | hp2 | a0001 | c0001 | t0007 | g0222 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19002 | hp1 | a0001 | c0001 | t0007 | g0132 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19004 | hp1 | a0001 | c0001 | t0007 | g0224 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0306 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19030 | hp1 | a0001 | c0001 | t0044 | g0340 | AFR | LWK | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19030 | hp2 | a0001 | c0001 | t0031 | g0117 | AFR | LWK | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | LWK | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19043 | hp2 | a0001 | c0001 | t0021 | g0263 | AFR | LWK | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0298 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19057 | hp2 | a0001 | c0001 | t0007 | g0130 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0318 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0337 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0316 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0315 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19065 | hp2 | a0001 | c0001 | t0007 | g0133 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19078 | hp1 | a0001 | c0001 | t0007 | g0221 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0323 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0285 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19086 | hp2 | a0001 | c0001 | t0038 | g0136 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19087 | hp1 | a0001 | c0001 | t0007 | g0226 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0303 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0030 | AFR | YRI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19240 | hp2 | a0001 | c0002 | t0012 | g0246 | AFR | YRI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20129 | hp1 | a0001 | c0001 | t0026 | g0293 | AFR | ASW | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ASW | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0103 | EUR | TSI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0080 | EUR | TSI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20805 | hp1 | a0001 | c0001 | t0013 | g0243 | EUR | TSI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | TSI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | GIH | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0094 | SAS | GIH | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02109 | hp2 | a0001 | c0001 | t0016 | g0008 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02486 | hp1 | a0001 | c0001 | t0027 | g0335 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0073 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03471 | hp1 | a0001 | c0001 | t0025 | g0284 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | USA | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG06807 | hp2 | a0001 | c0001 | t0021 | g0262 | AFR | USA | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18955 | hp1 | a0001 | c0001 | t0029 | g0067 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0330 | AFR | USA | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20300 | hp2 | a0001 | c0001 | t0011 | g0196 | AFR | USA | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA21309 | hp2 | a0001 | c0001 | t0009 | g0235 | AFR | LWK | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0013 | g0244 | REF | REF | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0048 | REF | REF | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180280528 | T | C | 1 | a0002 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.34A>G | p.Ser12Gly | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/12 | 317/4799 | 34/1275 | 12/424 | chr5 | 180280528 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180280499 | A | C | 1 | a0001c0002 | 2 | HG02630.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.63T>G | p.Thr21Thr | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/12 | 346/4799 | 63/1275 | 21/424 | chr5 | 180280499 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180233336 | T | A | 1 | a0001c0001t0029 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3048A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 3048 | chr5 | 180233336 | ||||||
| chr5:180233703 | T | A | 1 | a0001c0001t0037 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2681A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 2681 | chr5 | 180233703 | ||||||
| chr5:180233774 | C | T | 5 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0028 others(2): Show |
25 | HG01167.hp2 HG01243.hp2 HG02055.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2610G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 2610 | chr5 | 180233774 | ||||||
| chr5:180233784 | G | A | 1 | a0001c0001t0026 | 2 | HG02647.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2600C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 2600 | chr5 | 180233784 | ||||||
| chr5:180233786 | T | A | 22 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(19): Show |
104 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2598A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 2598 | chr5 | 180233786 | ||||||
| chr5:180234265 | C | G | 1 | a0001c0001t0036 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2119G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 2119 | chr5 | 180234265 | ||||||
| chr5:180234282 | C | T | 1 | a0001c0001t0030 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2102G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 2102 | chr5 | 180234282 | ||||||
| chr5:180234342 | G | A | 1 | a0001c0001t0045 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2042C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 2042 | chr5 | 180234342 | ||||||
| chr5:180234388 | T | C | 1 | a0001c0001t0026 | 2 | HG02647.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1996A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1996 | chr5 | 180234388 | ||||||
| chr5:180234434 | G | A | 1 | a0001c0001t0033 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1950C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1950 | chr5 | 180234434 | ||||||
| chr5:180234528 | C | T | 12 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0011 others(9): Show |
65 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1856G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1856 | chr5 | 180234528 | ||||||
| chr5:180234610 | A | C | 7 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0012 others(4): Show |
47 | HG00099.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1774T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1774 | chr5 | 180234610 | ||||||
| chr5:180234616 | G | A | 1 | a0001c0001t0034 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1768C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1768 | chr5 | 180234616 | ||||||
| chr5:180234686 | T | C | 1 | a0001c0001t0018 | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1698A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1698 | chr5 | 180234686 | ||||||
| chr5:180234692 | C | T | 12 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(9): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*1692G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1692 | chr5 | 180234692 | ||||||
| chr5:180234944 | A | G | 1 | a0001c0001t0018 | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1440T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1440 | chr5 | 180234944 | ||||||
| chr5:180235025 | C | T | 3 | a0001c0001t0011 a0001c0001t0023 a0001c0001t0045 |
8 | HG01192.hp1 HG02145.hp2 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1359G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1359 | chr5 | 180235025 | ||||||
| chr5:180235038 | C | G | 1 | a0001c0001t0028 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1346G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1346 | chr5 | 180235038 | ||||||
| chr5:180235057 | T | C | 1 | a0001c0001t0007 | 18 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1327A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1327 | chr5 | 180235057 | ||||||
| chr5:180235172 | G | A | 1 | a0001c0001t0019 | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1212C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1212 | chr5 | 180235172 | ||||||
| chr5:180235358 | G | A | 1 | a0001c0001t0040 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1026C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1026 | chr5 | 180235358 | ||||||
| chr5:180235384 | A | G | 28 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(25): Show |
147 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*1000T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1000 | chr5 | 180235384 | ||||||
| chr5:180235579 | A | G | 2 | a0001c0001t0031 a0001c0001t0039 |
2 | HG01952.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*805T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 805 | chr5 | 180235579 | ||||||
| chr5:180235722 | C | A | 11 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(8): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*662G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 662 | chr5 | 180235722 | ||||||
| chr5:180235870 | A | G | 1 | a0001c0001t0024 | 2 | HG02258.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*514T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 514 | chr5 | 180235870 | ||||||
| chr5:180236148 | A | G | 1 | a0001c0001t0038 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*236T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 236 | chr5 | 180236148 | ||||||
| chr5:180236180 | C | T | 1 | a0001c0001t0017 | 4 | HG01243.hp1 HG03130.hp1 HG03490.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*204G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 204 | chr5 | 180236180 | ||||||
| chr5:180236251 | G | A | 23 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(20): Show |
121 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*133C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 133 | chr5 | 180236251 | ||||||
| chr5:180280585 | G | A | 1 | a0001c0001t0041 | 1 | HG02080.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-24C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/12 | chr5 | 180280585 | |||||||
| chr5:180291970 | C | CCCG | 3 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0028 |
23 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-173_-171dupCGG | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/12 | 11410 | chr5 | 180291970 | ||||||
| chr5:180291970 | CCCG | C | 25 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(22): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
5_prime_UTR_variant | MODIFIER | c.-173_-171delCGG | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/12 | 11410 | chr5 | 180291970 | ||||||
| chr5:180291970 | CCCGCCG | C | 6 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0014 others(3): Show |
55 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(52): Show |
5_prime_UTR_variant | MODIFIER | c.-176_-171delCGGCGG | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/12 | 11410 | chr5 | 180291970 | ||||||
| chr5:180292000 | G | A | 1 | a0001c0001t0042 | 1 | HG03710.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-200C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/12 | chr5 | 180292000 | |||||||
| chr5:180292003 | G | A | 1 | a0001c0001t0043 | 1 | NA18949.hp1 | 5_prime_UTR_variant | MODIFIER | c.-203C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/12 | 11442 | chr5 | 180292003 | ||||||
| chr5:180292057 | C | A | 3 | a0001c0001t0022 a0001c0001t0044 a0001c0001t0045 |
5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-257G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/12 | chr5 | 180292057 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180236614 | C | T | 113 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(110): Show |
121 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.1133-88G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180236614 | |||||||
| chr5:180236660 | A | C | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1133-134T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180236660 | |||||||
| chr5:180236967 | A | T | 8 | a0001c0001t0006g0035 a0001c0001t0006g0036 a0001c0001t0006g0037 others(5): Show |
8 | HG02071.hp1 NA18949.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.1133-441T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180236967 | |||||||
| chr5:180236999 | A | T | 16 | a0001c0001t0009g0002 a0001c0001t0009g0017 a0001c0001t0009g0018 others(13): Show |
22 | HG00639.hp2 HG01074.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1133-473T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180236999 | |||||||
| chr5:180237550 | C | T | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1132+782G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180237550 | |||||||
| chr5:180237693 | A | G | 1 | a0001c0001t0005g0304 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1132+639T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180237693 | |||||||
| chr5:180237814 | T | G | 29 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(26): Show |
30 | HG00099.hp2 HG01192.hp1 HG01975.hp2 others(27): Show |
intron_variant | MODIFIER | c.1132+518A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180237814 | |||||||
| chr5:180237909 | C | T | 5 | a0001c0001t0011g0196 a0001c0001t0011g0197 a0001c0001t0011g0198 others(2): Show |
5 | HG01192.hp1 HG02145.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1132+423G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180237909 | |||||||
| chr5:180237942 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1132+390C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180237942 | |||||||
| chr5:180237966 | G | A | 1 | a0001c0001t0008g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1132+366C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180237966 | |||||||
| chr5:180238019 | C | T | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1132+313G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238019 | |||||||
| chr5:180238047 | A | G | 133 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(130): Show |
147 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(144): Show |
intron_variant | MODIFIER | c.1132+285T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238047 | |||||||
| chr5:180238131 | A | G | 8 | a0001c0001t0011g0196 a0001c0001t0011g0197 a0001c0001t0011g0198 others(5): Show |
8 | HG01192.hp1 HG02145.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1132+201T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238131 | |||||||
| chr5:180238183 | T | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1132+149A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238183 | |||||||
| chr5:180238201 | C | T | 164 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(161): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1132+131G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238201 | |||||||
| chr5:180238224 | C | T | 14 | a0001c0001t0009g0002 a0001c0001t0009g0017 a0001c0001t0009g0018 others(11): Show |
20 | HG00639.hp2 HG01074.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1132+108G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238224 | |||||||
| chr5:180238225 | G | A | 5 | a0001c0001t0011g0196 a0001c0001t0011g0197 a0001c0001t0011g0198 others(2): Show |
5 | HG01192.hp1 HG02145.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1132+107C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238225 | |||||||
| chr5:180238226 | C | T | 2 | a0001c0001t0002g0055 a0001c0001t0002g0077 |
2 | HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1132+106G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238226 | |||||||
| chr5:180238230 | G | A | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1132+102C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238230 | |||||||
| chr5:180238572 | A | G | 313 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(310): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1061-169T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238572 | |||||||
| chr5:180238596 | TTTC | T | 40 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(37): Show |
41 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.1061-196_1061-194d others(5): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238596 | |||||||
| chr5:180238605 | CTTCT | C | 20 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(17): Show |
22 | HG01243.hp2 HG02055.hp2 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1061-206_1061-203d others(6): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238605 | |||||||
| chr5:180238608 | C | CT | 47 | a0001c0001t0001g0125 a0001c0001t0001g0158 a0001c0001t0001g0184 others(44): Show |
56 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.1061-206dupA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238608 | |||||||
| chr5:180238608 | CT | C | 21 | a0001c0001t0003g0108 a0001c0001t0007g0013 a0001c0001t0007g0130 others(18): Show |
22 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.1061-206delA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238608 | |||||||
| chr5:180238611 | T | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0187 a0001c0001t0001g0190 |
3 | HG01175.hp1 HG01993.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1061-208A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238611 | |||||||
| chr5:180238687 | A | C | 133 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(130): Show |
147 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(144): Show |
intron_variant | MODIFIER | c.1061-284T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238687 | |||||||
| chr5:180238836 | T | C | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1061-433A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238836 | |||||||
| chr5:180239177 | T | C | 1 | a0001c0001t0004g0315 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1060+747A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180239177 | |||||||
| chr5:180239262 | C | T | 2 | a0001c0001t0012g0240 a0001c0001t0012g0241 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1060+662G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180239262 | |||||||
| chr5:180239446 | C | A | 3 | a0001c0001t0011g0218 a0001c0001t0023g0121 a0001c0001t0023g0122 |
3 | HG02965.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1060+478G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180239446 | |||||||
| chr5:180239634 | A | G | 2 | a0001c0002t0012g0245 a0001c0002t0012g0246 |
2 | HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1060+290T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180239634 | |||||||
| chr5:180239641 | T | G | 2 | a0001c0002t0012g0245 a0001c0002t0012g0246 |
2 | HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1060+283A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180239641 | |||||||
| chr5:180239813 | G | A | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1060+111C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180239813 | |||||||
| chr5:180239827 | C | T | 1 | a0001c0001t0010g0047 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1060+97G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180239827 | |||||||
| chr5:180240000 | T | C | 2 | a0001c0001t0031g0117 a0001c0001t0039g0242 |
2 | HG01952.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.997-13A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240000 | |||||||
| chr5:180240101 | T | C | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.997-114A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240101 | |||||||
| chr5:180240176 | A | C | 1 | a0001c0001t0031g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.997-189T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240176 | |||||||
| chr5:180240231 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.997-244G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240231 | |||||||
| chr5:180240292 | A | G | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.997-305T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240292 | |||||||
| chr5:180240327 | G | A | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.997-340C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240327 | |||||||
| chr5:180240589 | C | T | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.996+442G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240589 | |||||||
| chr5:180240708 | T | G | 1 | a0001c0001t0004g0332 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.996+323A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240708 | |||||||
| chr5:180240733 | A | T | 1 | a0001c0001t0001g0163 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.996+298T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240733 | |||||||
| chr5:180240806 | G | A | 52 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(49): Show |
55 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.996+225C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240806 | |||||||
| chr5:180240933 | C | G | 77 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(74): Show |
86 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.996+98G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240933 | |||||||
| chr5:180241304 | A | ATT | 19 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(16): Show |
20 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.872-151_872-150dup others(2): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241304 | |||||||
| chr5:180241305 | T | A | 10 | a0001c0001t0001g0144 a0001c0001t0001g0162 a0001c0001t0001g0179 others(7): Show |
10 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.872-150A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241305 | |||||||
| chr5:180241313 | T | C | 1 | a0001c0001t0010g0103 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.872-158A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241313 | |||||||
| chr5:180241327 | C | T | 17 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(14): Show |
18 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.872-172G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241327 | |||||||
| chr5:180241334 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.872-179A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241334 | |||||||
| chr5:180241344 | G | A | 1 | a0001c0001t0003g0085 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.872-189C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241344 | |||||||
| chr5:180241389 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.872-234G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241389 | |||||||
| chr5:180241391 | G | A | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.872-236C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241391 | |||||||
| chr5:180241423 | A | G | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.872-268T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241423 | |||||||
| chr5:180241494 | T | A | 1 | a0001c0001t0021g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.872-339A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241494 | |||||||
| chr5:180241542 | G | A | 2 | a0001c0001t0004g0312 a0001c0001t0004g0313 |
2 | HG01934.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.872-387C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241542 | |||||||
| chr5:180241708 | T | C | 133 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(130): Show |
147 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(144): Show |
intron_variant | MODIFIER | c.872-553A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241708 | |||||||
| chr5:180241823 | C | T | 2 | a0001c0001t0004g0319 a0001c0001t0004g0320 |
2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.872-668G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241823 | |||||||
| chr5:180242066 | C | T | 21 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(18): Show |
22 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.871+507G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180242066 | |||||||
| chr5:180242075 | G | C | 9 | a0001c0001t0001g0152 a0001c0001t0001g0186 a0001c0001t0001g0187 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.871+498C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180242075 | |||||||
| chr5:180242330 | A | G | 1 | a0001c0001t0005g0295 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.871+243T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180242330 | |||||||
| chr5:180242461 | G | A | 2 | a0001c0001t0004g0319 a0001c0001t0004g0320 |
2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.871+112C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180242461 | |||||||
| chr5:180242798 | T | C | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.689-43A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180242798 | |||||||
| chr5:180242833 | T | G | 50 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(47): Show |
55 | HG00099.hp2 HG00733.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.689-78A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180242833 | |||||||
| chr5:180242845 | G | C | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.689-90C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180242845 | |||||||
| chr5:180242924 | T | G | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.689-169A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180242924 | |||||||
| chr5:180243087 | T | C | 9 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(6): Show |
9 | HG01952.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.689-332A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243087 | |||||||
| chr5:180243116 | T | C | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-361A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243116 | |||||||
| chr5:180243119 | T | G | 3 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0212 |
3 | HG01099.hp1 HG01928.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.689-364A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243119 | |||||||
| chr5:180243200 | T | C | 1 | a0001c0001t0032g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.689-445A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243200 | |||||||
| chr5:180243271 | T | C | 50 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(47): Show |
55 | HG00099.hp2 HG00733.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.689-516A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243271 | |||||||
| chr5:180243516 | A | G | 50 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(47): Show |
55 | HG00099.hp2 HG00733.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.689-761T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243516 | |||||||
| chr5:180243528 | C | T | 163 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(160): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.689-773G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243528 | |||||||
| chr5:180243531 | G | A | 1 | a0001c0001t0007g0267 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.689-776C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243531 | |||||||
| chr5:180243647 | C | T | 2 | a0001c0001t0012g0240 a0001c0001t0012g0241 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.689-892G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243647 | |||||||
| chr5:180243727 | A | G | 1 | a0001c0001t0010g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.689-972T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243727 | |||||||
| chr5:180243761 | C | T | 7 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(4): Show |
7 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.689-1006G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243761 | |||||||
| chr5:180243850 | T | C | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.689-1095A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243850 | |||||||
| chr5:180243856 | T | C | 23 | a0001c0001t0001g0005 a0001c0001t0007g0013 a0001c0001t0007g0130 others(20): Show |
26 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.689-1101A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243856 | |||||||
| chr5:180244045 | C | T | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-1290G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244045 | |||||||
| chr5:180244069 | G | A | 1 | a0001c0001t0006g0027 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.689-1314C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244069 | |||||||
| chr5:180244212 | C | T | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.689-1457G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244212 | |||||||
| chr5:180244231 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.689-1476A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244231 | |||||||
| chr5:180244379 | T | C | 1 | a0001c0001t0031g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.689-1624A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244379 | |||||||
| chr5:180244443 | C | T | 1 | a0001c0001t0008g0079 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.689-1688G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244443 | |||||||
| chr5:180244444 | G | A | 1 | a0001c0001t0007g0134 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.689-1689C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244444 | |||||||
| chr5:180244482 | T | A | 10 | a0001c0001t0002g0080 a0001c0001t0002g0084 a0001c0001t0002g0086 others(7): Show |
10 | HG02258.hp2 HG02630.hp1 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.689-1727A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244482 | |||||||
| chr5:180244591 | C | T | 1 | a0001c0001t0013g0243 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.689-1836G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244591 | |||||||
| chr5:180244595 | G | A | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.689-1840C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244595 | |||||||
| chr5:180244607 | CT | C | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-1853delA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244607 | |||||||
| chr5:180244722 | T | C | 339 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(336): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.689-1967A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244722 | |||||||
| chr5:180244766 | T | A | 1 | a0001c0001t0002g0063 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.689-2011A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244766 | |||||||
| chr5:180244778 | GA | G | 106 | a0001c0001t0001g0158 a0001c0001t0001g0183 a0001c0001t0001g0189 others(103): Show |
116 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.689-2024delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244778 | |||||||
| chr5:180244778 | GAA | G | 157 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(154): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.689-2025_689-2024d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244778 | |||||||
| chr5:180244953 | C | T | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-2198G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244953 | |||||||
| chr5:180244954 | G | A | 2 | a0001c0001t0012g0240 a0001c0001t0012g0241 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.689-2199C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244954 | |||||||
| chr5:180245108 | G | A | 132 | a0001c0001t0002g0087 a0001c0001t0004g0021 a0001c0001t0004g0286 others(129): Show |
146 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(143): Show |
intron_variant | MODIFIER | c.688+2331C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245108 | |||||||
| chr5:180245305 | G | A | 1 | a0001c0001t0027g0334 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.688+2134C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245305 | |||||||
| chr5:180245440 | T | C | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.688+1999A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245440 | |||||||
| chr5:180245583 | C | T | 15 | a0001c0001t0002g0087 a0001c0001t0009g0002 a0001c0001t0009g0017 others(12): Show |
21 | HG00280.hp2 HG00639.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.688+1856G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245583 | |||||||
| chr5:180245588 | G | A | 1 | a0001c0001t0025g0284 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.688+1851C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245588 | |||||||
| chr5:180245825 | T | C | 134 | a0001c0001t0002g0087 a0001c0001t0004g0021 a0001c0001t0004g0286 others(131): Show |
148 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(145): Show |
intron_variant | MODIFIER | c.688+1614A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245825 | |||||||
| chr5:180245831 | G | A | 1 | a0001c0001t0010g0047 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.688+1608C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245831 | |||||||
| chr5:180245885 | A | G | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+1554T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245885 | |||||||
| chr5:180245960 | G | A | 4 | a0001c0001t0004g0286 a0001c0001t0004g0317 a0001c0001t0004g0323 others(1): Show |
4 | HG01934.hp2 NA18961.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.688+1479C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245960 | |||||||
| chr5:180245984 | C | T | 6 | a0001c0001t0002g0080 a0001c0001t0002g0086 a0001c0001t0002g0105 others(3): Show |
6 | HG03490.hp1 HG03669.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.688+1455G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245984 | |||||||
| chr5:180246104 | G | A | 2 | a0001c0001t0005g0336 a0001c0001t0005g0337 |
2 | NA18972.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.688+1335C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246104 | |||||||
| chr5:180246128 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.688+1311C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246128 | |||||||
| chr5:180246306 | G | C | 1 | a0001c0001t0001g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.688+1133C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246306 | |||||||
| chr5:180246506 | C | G | 4 | a0001c0001t0012g0240 a0001c0001t0012g0241 a0001c0002t0012g0245 others(1): Show |
4 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.688+933G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246506 | |||||||
| chr5:180246708 | T | C | 119 | a0001c0001t0002g0087 a0001c0001t0004g0021 a0001c0001t0004g0286 others(116): Show |
133 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(130): Show |
intron_variant | MODIFIER | c.688+731A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246708 | |||||||
| chr5:180246763 | TG | T | 17 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(14): Show |
18 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.688+675delC | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246763 | |||||||
| chr5:180246809 | T | C | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.688+630A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246809 | |||||||
| chr5:180246830 | A | C | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.688+609T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246830 | |||||||
| chr5:180246914 | A | G | 21 | a0001c0001t0008g0003 a0001c0001t0008g0010 a0001c0001t0008g0011 others(18): Show |
25 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.688+525T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246914 | |||||||
| chr5:180246955 | T | C | 1 | a0001c0001t0003g0094 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.688+484A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246955 | |||||||
| chr5:180247067 | C | T | 1 | a0001c0001t0003g0088 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.688+372G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180247067 | |||||||
| chr5:180247326 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.688+113T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180247326 | |||||||
| chr5:180247357 | G | A | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+82C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180247357 | |||||||
| chr5:180247668 | T | C | 1 | a0001c0001t0028g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.617-158A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180247668 | |||||||
| chr5:180248011 | G | A | 1 | a0001c0001t0011g0196 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.617-501C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248011 | |||||||
| chr5:180248052 | C | A | 27 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(24): Show |
28 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.617-542G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248052 | |||||||
| chr5:180248178 | C | T | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.617-668G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248178 | |||||||
| chr5:180248256 | A | C | 9 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(6): Show |
9 | HG01952.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.616+717T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248256 | |||||||
| chr5:180248442 | T | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0248 a0001c0001t0001g0249 |
4 | HG02896.hp1 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.616+531A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248442 | |||||||
| chr5:180248488 | T | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.616+485A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248488 | |||||||
| chr5:180248594 | T | C | 1 | a0001c0001t0011g0218 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.616+379A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248594 | |||||||
| chr5:180248726 | T | C | 1 | a0001c0001t0032g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.616+247A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248726 | |||||||
| chr5:180249367 | T | C | 1 | a0001c0001t0002g0118 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.451-229A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249367 | |||||||
| chr5:180249386 | G | A | 2 | a0001c0001t0004g0330 a0001c0001t0004g0331 |
2 | HG01109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.451-248C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249386 | |||||||
| chr5:180249432 | C | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0128 a0001c0001t0001g0139 others(2): Show |
6 | HG00408.hp2 HG02155.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-294G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249432 | |||||||
| chr5:180249432 | C | T | 41 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(38): Show |
49 | HG00639.hp2 HG01074.hp2 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.451-294G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249432 | |||||||
| chr5:180249473 | C | T | 1 | a0001c0001t0021g0263 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.451-335G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249473 | |||||||
| chr5:180249518 | G | GCTCT | 133 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(130): Show |
147 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(144): Show |
intron_variant | MODIFIER | c.451-381_451-380ins others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249518 | |||||||
| chr5:180249649 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.451-511A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249649 | |||||||
| chr5:180249651 | T | C | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0165 others(1): Show |
4 | HG00140.hp2 HG01516.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-513A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249651 | |||||||
| chr5:180249661 | C | T | 41 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(38): Show |
49 | HG00639.hp2 HG01074.hp2 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.451-523G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249661 | |||||||
| chr5:180249758 | C | T | 17 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(14): Show |
18 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.451-620G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249758 | |||||||
| chr5:180249760 | A | G | 6 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(3): Show |
6 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-622T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249760 | |||||||
| chr5:180249798 | C | T | 21 | a0001c0001t0008g0003 a0001c0001t0008g0010 a0001c0001t0008g0011 others(18): Show |
25 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.451-660G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249798 | |||||||
| chr5:180249875 | G | A | 2 | a0001c0001t0004g0286 a0001c0001t0004g0323 |
2 | NA19084.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.451-737C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249875 | |||||||
| chr5:180249937 | A | G | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.451-799T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249937 | |||||||
| chr5:180249979 | C | T | 50 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(47): Show |
58 | HG00639.hp2 HG01074.hp2 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.451-841G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249979 | |||||||
| chr5:180250029 | C | T | 21 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(18): Show |
22 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.451-891G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250029 | |||||||
| chr5:180250037 | C | T | 1 | a0001c0001t0005g0298 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.451-899G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250037 | |||||||
| chr5:180250051 | G | A | 2 | a0001c0001t0007g0224 a0001c0001t0007g0225 |
2 | NA18966.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.451-913C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250051 | |||||||
| chr5:180250082 | C | T | 1 | a0001c0001t0021g0263 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.451-944G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250082 | |||||||
| chr5:180250119 | C | T | 3 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 |
3 | HG01109.hp2 HG01346.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.451-981G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250119 | |||||||
| chr5:180250285 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.451-1147G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250285 | |||||||
| chr5:180250494 | C | A | 1 | a0001c0001t0013g0247 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.451-1356G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250494 | |||||||
| chr5:180250517 | G | A | 75 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(72): Show |
84 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.451-1379C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250517 | |||||||
| chr5:180250545 | C | T | 281 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.451-1407G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250545 | |||||||
| chr5:180250555 | T | C | 31 | a0001c0001t0001g0147 a0001c0001t0003g0043 a0001c0001t0004g0021 others(28): Show |
32 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.451-1417A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250555 | |||||||
| chr5:180250778 | C | G | 22 | a0001c0001t0008g0003 a0001c0001t0008g0010 a0001c0001t0008g0011 others(19): Show |
26 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.451-1640G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250778 | |||||||
| chr5:180250821 | G | A | 1 | a0001c0001t0039g0242 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.451-1683C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250821 | |||||||
| chr5:180250842 | G | A | 8 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-1704C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250842 | |||||||
| chr5:180250866 | C | T | 1 | a0001c0001t0014g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.451-1728G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250866 | |||||||
| chr5:180250940 | T | G | 18 | a0001c0001t0008g0003 a0001c0001t0008g0010 a0001c0001t0008g0011 others(15): Show |
22 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.451-1802A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250940 | |||||||
| chr5:180250985 | C | CA | 8 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-1848dupT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250985 | |||||||
| chr5:180250989 | G | C | 1 | a0001c0001t0001g0279 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.451-1851C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250989 | |||||||
| chr5:180251089 | A | C | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.451-1951T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251089 | |||||||
| chr5:180251113 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.451-1975C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251113 | |||||||
| chr5:180251127 | A | G | 1 | a0001c0001t0044g0340 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.451-1989T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251127 | |||||||
| chr5:180251290 | G | A | 1 | a0001c0001t0040g0208 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.451-2152C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251290 | |||||||
| chr5:180251310 | C | T | 3 | a0001c0001t0012g0206 a0001c0001t0032g0111 a0001c0001t0039g0242 |
3 | HG01952.hp2 HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.451-2172G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251310 | |||||||
| chr5:180251405 | C | T | 23 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(20): Show |
25 | HG01167.hp2 HG01243.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.451-2267G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251405 | |||||||
| chr5:180251573 | C | T | 1 | a0001c0001t0012g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.451-2435G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251573 | |||||||
| chr5:180251602 | C | T | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-2464G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251602 | |||||||
| chr5:180251603 | G | A | 27 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(24): Show |
28 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.451-2465C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251603 | |||||||
| chr5:180251617 | G | A | 17 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(14): Show |
18 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.451-2479C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251617 | |||||||
| chr5:180251665 | C | T | 1 | a0001c0001t0013g0265 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.451-2527G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251665 | |||||||
| chr5:180251732 | A | AGTGACGC others(12): Show |
1 | a0001c0001t0008g0057 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.451-2595_451-2594i others(21): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251732 | |||||||
| chr5:180251732 | A | AGTGACGC others(12): Show |
80 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(77): Show |
87 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.451-2613_451-2595d others(21): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251732 | |||||||
| chr5:180251811 | C | T | 3 | a0001c0001t0014g0309 a0001c0001t0014g0310 a0001c0001t0025g0284 |
3 | HG03130.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.451-2673G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251811 | |||||||
| chr5:180251927 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0003g0043 |
2 | HG00558.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.451-2789G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251927 | |||||||
| chr5:180252021 | C | T | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.451-2883G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252021 | |||||||
| chr5:180252071 | C | T | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.451-2933G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252071 | |||||||
| chr5:180252085 | C | T | 1 | a0001c0001t0009g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.451-2947G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252085 | |||||||
| chr5:180252144 | C | T | 46 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(43): Show |
52 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.451-3006G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252144 | |||||||
| chr5:180252183 | A | G | 7 | a0001c0001t0012g0206 a0001c0001t0018g0123 a0001c0001t0018g0124 others(4): Show |
7 | HG01099.hp1 HG01928.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.451-3045T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252183 | |||||||
| chr5:180252237 | T | C | 2 | a0001c0001t0001g0273 a0001c0001t0001g0280 |
2 | HG03927.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.451-3099A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252237 | |||||||
| chr5:180252315 | C | T | 1 | a0001c0001t0039g0242 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.451-3177G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252315 | |||||||
| chr5:180252350 | C | T | 46 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(43): Show |
52 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.451-3212G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252350 | |||||||
| chr5:180252504 | C | T | 46 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(43): Show |
52 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.451-3366G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252504 | |||||||
| chr5:180252652 | C | T | 1 | a0001c0001t0020g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.451-3514G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252652 | |||||||
| chr5:180252726 | G | A | 8 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-3588C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252726 | |||||||
| chr5:180252744 | G | A | 8 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-3606C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252744 | |||||||
| chr5:180252760 | C | A | 124 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0125 others(121): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.451-3622G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252760 | |||||||
| chr5:180252763 | G | A | 4 | a0001c0001t0011g0218 a0001c0001t0023g0121 a0001c0001t0023g0122 others(1): Show |
4 | HG02145.hp2 HG02965.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-3625C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252763 | |||||||
| chr5:180252833 | T | C | 3 | a0001c0001t0012g0206 a0001c0001t0032g0111 a0001c0001t0039g0242 |
3 | HG01952.hp2 HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.451-3695A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252833 | |||||||
| chr5:180252848 | C | T | 4 | a0001c0001t0011g0218 a0001c0001t0023g0121 a0001c0001t0023g0122 others(1): Show |
4 | HG02145.hp2 HG02965.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-3710G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252848 | |||||||
| chr5:180252980 | G | T | 27 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(24): Show |
28 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.451-3842C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252980 | |||||||
| chr5:180253039 | G | A | 3 | a0001c0001t0005g0292 a0001c0001t0015g0022 a0001c0001t0015g0023 |
3 | HG02055.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.451-3901C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253039 | |||||||
| chr5:180253076 | T | C | 90 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(87): Show |
97 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.451-3938A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253076 | |||||||
| chr5:180253078 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.451-3940G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253078 | |||||||
| chr5:180253115 | G | A | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.451-3977C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253115 | |||||||
| chr5:180253172 | C | T | 90 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(87): Show |
97 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.451-4034G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253172 | |||||||
| chr5:180253228 | G | A | 1 | a0001c0001t0009g0232 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.451-4090C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253228 | |||||||
| chr5:180253233 | A | G | 298 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(295): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.451-4095T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253233 | |||||||
| chr5:180253310 | C | T | 11 | a0001c0001t0002g0080 a0001c0001t0002g0084 a0001c0001t0002g0086 others(8): Show |
11 | HG00280.hp2 HG02258.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.451-4172G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253310 | |||||||
| chr5:180253311 | G | A | 18 | a0001c0001t0001g0270 a0001c0001t0007g0013 a0001c0001t0007g0130 others(15): Show |
19 | HG00099.hp2 HG00642.hp1 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.451-4173C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253311 | |||||||
| chr5:180253343 | G | A | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.451-4205C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253343 | |||||||
| chr5:180253361 | G | A | 1 | a0001c0001t0041g0302 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.451-4223C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253361 | |||||||
| chr5:180253666 | G | A | 1 | a0001c0001t0039g0242 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.451-4528C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253666 | |||||||
| chr5:180253820 | T | C | 1 | a0001c0001t0002g0115 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.451-4682A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253820 | |||||||
| chr5:180253896 | GAC | G | 166 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(163): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.451-4760_451-4759d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253896 | |||||||
| chr5:180253906 | C | T | 46 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(43): Show |
52 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.451-4768G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253906 | |||||||
| chr5:180253961 | C | CT | 4 | a0001c0001t0011g0196 a0001c0001t0011g0197 a0001c0001t0011g0198 others(1): Show |
4 | HG01192.hp1 HG03710.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-4824dupA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253961 | |||||||
| chr5:180253963 | C | CT | 83 | a0001c0001t0002g0116 a0001c0001t0002g0118 a0001c0001t0004g0021 others(80): Show |
90 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.451-4826dupA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253963 | |||||||
| chr5:180253963 | C | CTT | 25 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0182 others(22): Show |
31 | HG00609.hp1 HG00639.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.451-4827_451-4826d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253963 | |||||||
| chr5:180253963 | C | CTTT | 149 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(146): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.451-4828_451-4826d others(5): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253963 | |||||||
| chr5:180253963 | C | CTTTT | 6 | a0001c0001t0001g0162 a0001c0001t0001g0189 a0001c0001t0001g0193 others(3): Show |
6 | HG02148.hp2 HG03516.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-4829_451-4826d others(6): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253963 | |||||||
| chr5:180253963 | C | T | 4 | a0001c0001t0011g0196 a0001c0001t0011g0197 a0001c0001t0011g0198 others(1): Show |
4 | HG01192.hp1 HG03710.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-4825G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253963 | |||||||
| chr5:180254004 | T | G | 8 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-4866A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254004 | |||||||
| chr5:180254124 | G | C | 1 | a0001c0001t0037g0281 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.451-4986C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254124 | |||||||
| chr5:180254216 | C | T | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.451-5078G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254216 | |||||||
| chr5:180254351 | G | A | 339 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(336): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.451-5213C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254351 | |||||||
| chr5:180254423 | A | G | 1 | a0001c0001t0003g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.451-5285T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254423 | |||||||
| chr5:180254497 | G | A | 5 | a0001c0001t0011g0218 a0001c0001t0023g0121 a0001c0001t0023g0122 others(2): Show |
5 | HG02145.hp2 HG02965.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-5359C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254497 | |||||||
| chr5:180254514 | A | G | 46 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(43): Show |
52 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.451-5376T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254514 | |||||||
| chr5:180254801 | G | A | 74 | a0001c0001t0002g0105 a0001c0001t0004g0021 a0001c0001t0004g0286 others(71): Show |
81 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.451-5663C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254801 | |||||||
| chr5:180254890 | T | G | 3 | a0001c0001t0012g0206 a0001c0001t0032g0111 a0001c0001t0039g0242 |
3 | HG01952.hp2 HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.451-5752A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254890 | |||||||
| chr5:180254903 | G | A | 5 | a0001c0001t0001g0185 a0001c0001t0001g0202 a0001c0001t0012g0206 others(2): Show |
5 | HG01952.hp2 HG02145.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-5765C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254903 | |||||||
| chr5:180254957 | C | T | 1 | a0001c0001t0004g0325 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.451-5819G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254957 | |||||||
| chr5:180255063 | C | T | 8 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-5925G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255063 | |||||||
| chr5:180255174 | C | T | 72 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(69): Show |
79 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.451-6036G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255174 | |||||||
| chr5:180255205 | C | T | 1 | a0001c0001t0004g0314 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.451-6067G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255205 | |||||||
| chr5:180255266 | G | A | 5 | a0001c0001t0003g0090 a0001c0001t0011g0218 a0001c0001t0023g0121 others(2): Show |
5 | HG02145.hp2 HG02965.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-6128C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255266 | |||||||
| chr5:180255287 | A | G | 31 | a0001c0001t0001g0005 a0001c0001t0003g0090 a0001c0001t0007g0013 others(28): Show |
34 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.451-6149T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255287 | |||||||
| chr5:180255412 | A | G | 298 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(295): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.450+6272T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255412 | |||||||
| chr5:180255444 | C | T | 1 | a0001c0001t0008g0079 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.450+6240G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255444 | |||||||
| chr5:180255482 | A | G | 117 | a0001c0001t0001g0005 a0001c0001t0004g0021 a0001c0001t0004g0286 others(114): Show |
127 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.450+6202T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255482 | |||||||
| chr5:180255493 | G | C | 72 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(69): Show |
79 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.450+6191C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255493 | |||||||
| chr5:180255508 | C | T | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.450+6176G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255508 | |||||||
| chr5:180255599 | G | T | 1 | a0001c0001t0004g0328 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.450+6085C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255599 | |||||||
| chr5:180255667 | G | A | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+6017C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255667 | |||||||
| chr5:180255832 | T | C | 115 | a0001c0001t0001g0005 a0001c0001t0004g0021 a0001c0001t0004g0286 others(112): Show |
125 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.450+5852A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255832 | |||||||
| chr5:180255993 | C | T | 5 | a0001c0001t0001g0170 a0001c0001t0002g0061 a0001c0001t0005g0287 others(2): Show |
5 | HG00544.hp2 HG00609.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+5691G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255993 | |||||||
| chr5:180256162 | G | A | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+5522C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180256162 | |||||||
| chr5:180256278 | T | C | 8 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+5406A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180256278 | |||||||
| chr5:180256294 | T | C | 1 | a0001c0001t0040g0208 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.450+5390A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180256294 | |||||||
| chr5:180256634 | A | G | 339 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(336): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.450+5050T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180256634 | |||||||
| chr5:180256673 | G | A | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.450+5011C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180256673 | |||||||
| chr5:180256717 | G | A | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.450+4967C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180256717 | |||||||
| chr5:180256868 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.450+4816C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180256868 | |||||||
| chr5:180257148 | C | T | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.450+4536G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257148 | |||||||
| chr5:180257233 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.450+4451G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257233 | |||||||
| chr5:180257248 | C | G | 2 | a0001c0001t0024g0260 a0001c0001t0024g0261 |
2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.450+4436G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257248 | |||||||
| chr5:180257427 | C | T | 80 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(77): Show |
87 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.450+4257G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257427 | |||||||
| chr5:180257433 | C | T | 180 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(177): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.450+4251G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257433 | |||||||
| chr5:180257455 | G | A | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+4229C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257455 | |||||||
| chr5:180257583 | G | A | 1 | a0001c0001t0004g0322 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.450+4101C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257583 | |||||||
| chr5:180257627 | T | A | 1 | a0001c0001t0005g0296 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.450+4057A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257627 | |||||||
| chr5:180257864 | G | A | 1 | a0001c0001t0005g0296 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.450+3820C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257864 | |||||||
| chr5:180257868 | A | T | 339 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(336): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.450+3816T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257868 | |||||||
| chr5:180258139 | T | A | 1 | a0001c0001t0002g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.450+3545A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258139 | |||||||
| chr5:180258313 | T | C | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+3371A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258313 | |||||||
| chr5:180258331 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.450+3353G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258331 | |||||||
| chr5:180258514 | C | T | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+3170G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258514 | |||||||
| chr5:180258515 | G | A | 1 | a0001c0001t0032g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.450+3169C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258515 | |||||||
| chr5:180258523 | T | C | 2 | a0001c0001t0008g0046 a0001c0001t0020g0228 |
2 | HG03927.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.450+3161A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258523 | |||||||
| chr5:180258683 | G | C | 3 | a0001c0001t0001g0185 a0001c0001t0001g0193 a0001c0001t0001g0202 |
3 | NA18946.hp2 NA18965.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.450+3001C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258683 | |||||||
| chr5:180258697 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0003g0085 |
2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.450+2987G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258697 | |||||||
| chr5:180258853 | T | C | 339 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(336): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.450+2831A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258853 | |||||||
| chr5:180258862 | T | TA | 97 | a0001c0001t0001g0005 a0001c0001t0001g0126 a0001c0001t0001g0127 others(94): Show |
107 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.450+2821dupT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258862 | |||||||
| chr5:180258862 | T | TAA | 13 | a0001c0001t0004g0325 a0001c0001t0004g0326 a0001c0001t0004g0328 others(10): Show |
13 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.450+2820_450+2821d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258862 | |||||||
| chr5:180258862 | TA | T | 11 | a0001c0001t0001g0173 a0001c0001t0001g0181 a0001c0001t0001g0209 others(8): Show |
11 | HG01256.hp2 HG02451.hp2 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.450+2821delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258862 | |||||||
| chr5:180259033 | CA | C | 112 | a0001c0001t0001g0005 a0001c0001t0003g0097 a0001c0001t0004g0021 others(109): Show |
122 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.450+2650delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259033 | |||||||
| chr5:180259083 | T | C | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.450+2601A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259083 | |||||||
| chr5:180259114 | AACCCTTT others(77): Show |
A | 1 | a0001c0001t0006g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.450+2486_450+2569d others(86): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259114 | |||||||
| chr5:180259138 | G | C | 1 | a0001c0001t0028g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.450+2546C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259138 | |||||||
| chr5:180259163 | T | C | 1 | a0001c0001t0003g0119 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.450+2521A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259163 | |||||||
| chr5:180259168 | G | C | 8 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0095 others(5): Show |
10 | HG01255.hp1 HG01256.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.450+2516C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259168 | |||||||
| chr5:180259251 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.450+2433A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259251 | |||||||
| chr5:180259264 | G | A | 8 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+2420C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259264 | |||||||
| chr5:180259266 | A | T | 8 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+2418T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259266 | |||||||
| chr5:180259335 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.450+2349G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259335 | |||||||
| chr5:180259352 | T | G | 1 | a0001c0001t0003g0071 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.450+2332A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259352 | |||||||
| chr5:180259374 | G | C | 2 | a0001c0001t0012g0240 a0001c0001t0012g0241 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.450+2310C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259374 | |||||||
| chr5:180259378 | G | A | 80 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(77): Show |
87 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.450+2306C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259378 | |||||||
| chr5:180259404 | C | T | 3 | a0001c0001t0021g0262 a0001c0001t0024g0260 a0001c0001t0024g0261 |
3 | HG02258.hp2 HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.450+2280G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259404 | |||||||
| chr5:180259525 | C | T | 1 | a0001c0001t0015g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.450+2159G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259525 | |||||||
| chr5:180259560 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.450+2124G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259560 | |||||||
| chr5:180259779 | A | G | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.450+1905T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259779 | |||||||
| chr5:180259796 | C | A | 2 | a0001c0001t0001g0146 a0001c0001t0035g0145 |
2 | HG00621.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.450+1888G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259796 | |||||||
| chr5:180259816 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.450+1868A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259816 | |||||||
| chr5:180259882 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.450+1802G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259882 | |||||||
| chr5:180259917 | G | C | 1 | a0001c0001t0024g0261 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+1767C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259917 | |||||||
| chr5:180259983 | G | A | 1 | a0001c0001t0009g0234 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.450+1701C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259983 | |||||||
| chr5:180260013 | T | C | 73 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(70): Show |
80 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.450+1671A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260013 | |||||||
| chr5:180260095 | C | G | 17 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(14): Show |
18 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.450+1589G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260095 | |||||||
| chr5:180260166 | T | C | 1 | a0001c0001t0003g0089 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.450+1518A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260166 | |||||||
| chr5:180260187 | A | G | 2 | a0001c0001t0022g0341 a0001c0001t0022g0343 |
2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.450+1497T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260187 | |||||||
| chr5:180260223 | G | A | 2 | a0001c0001t0012g0206 a0001c0001t0032g0111 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.450+1461C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260223 | |||||||
| chr5:180260247 | G | C | 1 | a0001c0001t0007g0134 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.450+1437C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260247 | |||||||
| chr5:180260257 | A | G | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+1427T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260257 | |||||||
| chr5:180260294 | A | G | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+1390T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260294 | |||||||
| chr5:180260564 | G | A | 3 | a0001c0001t0005g0292 a0001c0001t0015g0022 a0001c0001t0015g0023 |
3 | HG02055.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.450+1120C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260564 | |||||||
| chr5:180260576 | G | A | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.450+1108C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260576 | |||||||
| chr5:180260624 | T | A | 1 | a0001c0001t0001g0282 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.450+1060A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260624 | |||||||
| chr5:180260685 | A | G | 110 | a0001c0001t0001g0005 a0001c0001t0004g0021 a0001c0001t0004g0286 others(107): Show |
120 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.450+999T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260685 | |||||||
| chr5:180260772 | C | T | 179 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(176): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.450+912G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260772 | |||||||
| chr5:180260928 | T | C | 1 | a0001c0001t0032g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.450+756A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260928 | |||||||
| chr5:180260943 | GA | G | 112 | a0001c0001t0001g0005 a0001c0001t0004g0021 a0001c0001t0004g0286 others(109): Show |
122 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.450+740delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260943 | |||||||
| chr5:180261090 | A | G | 2 | a0001c0001t0006g0032 a0001c0001t0006g0042 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.450+594T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261090 | |||||||
| chr5:180261140 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.450+544G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261140 | |||||||
| chr5:180261192 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.450+492G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261192 | |||||||
| chr5:180261356 | T | C | 1 | a0001c0001t0010g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.450+328A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261356 | |||||||
| chr5:180261447 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.450+237G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261447 | |||||||
| chr5:180261478 | C | T | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.450+206G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261478 | |||||||
| chr5:180261542 | A | G | 3 | a0001c0001t0017g0014 a0001c0001t0017g0154 a0001c0001t0017g0155 |
4 | HG01243.hp1 HG03130.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+142T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261542 | |||||||
| chr5:180261556 | C | T | 12 | a0001c0001t0009g0002 a0001c0001t0009g0017 a0001c0001t0009g0018 others(9): Show |
17 | HG00639.hp2 HG01074.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.450+128G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261556 | |||||||
| chr5:180261559 | T | C | 1 | a0001c0001t0039g0242 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.450+125A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261559 | |||||||
| chr5:180261606 | A | T | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.450+78T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261606 | |||||||
| chr5:180261920 | G | C | 1 | a0001c0001t0001g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.312-98C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180261920 | |||||||
| chr5:180262027 | A | C | 12 | a0001c0001t0004g0312 a0001c0001t0004g0313 a0001c0001t0004g0324 others(9): Show |
12 | HG00639.hp1 HG00642.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.312-205T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262027 | |||||||
| chr5:180262028 | C | A | 1 | a0001c0001t0039g0242 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.312-206G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262028 | |||||||
| chr5:180262144 | A | G | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.312-322T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262144 | |||||||
| chr5:180262259 | A | G | 2 | a0001c0001t0007g0224 a0001c0001t0007g0225 |
2 | NA18966.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.312-437T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262259 | |||||||
| chr5:180262289 | A | G | 20 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0051 others(17): Show |
23 | HG00099.hp1 HG00423.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.312-467T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262289 | |||||||
| chr5:180262308 | C | A | 1 | a0001c0001t0004g0324 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.312-486G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262308 | |||||||
| chr5:180262386 | GA | G | 178 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(175): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.312-565delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262386 | |||||||
| chr5:180262521 | G | A | 21 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0049 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.312-699C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262521 | |||||||
| chr5:180262570 | T | TA | 117 | a0001c0001t0001g0005 a0001c0001t0001g0238 a0001c0001t0002g0080 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.312-749dupT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262570 | |||||||
| chr5:180262627 | G | C | 4 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.312-805C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262627 | |||||||
| chr5:180262662 | C | A | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.312-840G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262662 | |||||||
| chr5:180262764 | T | C | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.312-942A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262764 | |||||||
| chr5:180262866 | C | A | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.312-1044G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262866 | |||||||
| chr5:180262867 | G | A | 8 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.312-1045C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262867 | |||||||
| chr5:180262898 | G | C | 23 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(20): Show |
25 | HG01167.hp2 HG01243.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.312-1076C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262898 | |||||||
| chr5:180263025 | G | C | 1 | a0001c0001t0003g0097 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.312-1203C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263025 | |||||||
| chr5:180263354 | C | T | 56 | a0001c0001t0004g0312 a0001c0001t0004g0313 a0001c0001t0004g0324 others(53): Show |
62 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.311+1427G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263354 | |||||||
| chr5:180263401 | C | T | 56 | a0001c0001t0004g0312 a0001c0001t0004g0313 a0001c0001t0004g0324 others(53): Show |
62 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.311+1380G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263401 | |||||||
| chr5:180263653 | T | C | 1 | a0001c0001t0039g0242 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.311+1128A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263653 | |||||||
| chr5:180263706 | C | CT | 150 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0126 others(147): Show |
165 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.311+1074dupA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263706 | |||||||
| chr5:180263706 | C | CTT | 136 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0125 others(133): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.311+1073_311+1074d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263706 | |||||||
| chr5:180263706 | C | CTTT | 20 | a0001c0001t0001g0005 a0001c0001t0001g0258 a0001c0001t0001g0271 others(17): Show |
23 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.311+1072_311+1074d others(5): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263706 | |||||||
| chr5:180263749 | T | C | 3 | a0001c0001t0006g0027 a0001c0001t0006g0029 a0001c0001t0006g0030 |
3 | HG01167.hp2 HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.311+1032A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263749 | |||||||
| chr5:180263863 | G | A | 17 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(14): Show |
18 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.311+918C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263863 | |||||||
| chr5:180263932 | C | T | 1 | a0001c0001t0021g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.311+849G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263932 | |||||||
| chr5:180264011 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.311+770T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180264011 | |||||||
| chr5:180264145 | T | C | 3 | a0001c0001t0012g0206 a0001c0001t0032g0111 a0001c0001t0039g0242 |
3 | HG01952.hp2 HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.311+636A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180264145 | |||||||
| chr5:180264468 | C | T | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.311+313G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180264468 | |||||||
| chr5:180264715 | T | C | 1 | a0001c0001t0007g0219 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.311+66A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180264715 | |||||||
| chr5:180264923 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.253-84G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180264923 | |||||||
| chr5:180264951 | ACTT | A | 99 | a0001c0001t0001g0005 a0001c0001t0004g0021 a0001c0001t0004g0286 others(96): Show |
105 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.253-115_253-113del others(3): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180264951 | |||||||
| chr5:180265019 | A | C | 1 | a0001c0001t0027g0334 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.253-180T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265019 | |||||||
| chr5:180265023 | G | A | 3 | a0001c0001t0011g0218 a0001c0001t0023g0121 a0001c0001t0023g0122 |
3 | HG02965.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.253-184C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265023 | |||||||
| chr5:180265024 | C | T | 1 | a0001c0001t0024g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.253-185G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265024 | |||||||
| chr5:180265039 | C | T | 3 | a0001c0001t0013g0247 a0001c0001t0026g0291 a0001c0001t0026g0293 |
3 | HG02647.hp1 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.253-200G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265039 | |||||||
| chr5:180265078 | T | G | 1 | a0001c0001t0039g0242 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.253-239A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265078 | |||||||
| chr5:180265419 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.253-580C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265419 | |||||||
| chr5:180265566 | C | T | 21 | a0001c0001t0002g0080 a0001c0001t0002g0084 a0001c0001t0002g0086 others(18): Show |
22 | HG00280.hp2 HG02258.hp2 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.253-727G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265566 | |||||||
| chr5:180265587 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | NA18966.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.253-748C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265587 | |||||||
| chr5:180265682 | C | T | 2 | a0001c0001t0012g0240 a0001c0001t0012g0241 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.253-843G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265682 | |||||||
| chr5:180265698 | C | A | 1 | a0001c0001t0003g0119 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.253-859G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265698 | |||||||
| chr5:180265799 | G | A | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-960C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265799 | |||||||
| chr5:180265891 | T | A | 1 | a0001c0001t0009g0018 | 2 | HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.253-1052A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265891 | |||||||
| chr5:180265945 | C | T | 339 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(336): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.253-1106G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265945 | |||||||
| chr5:180266062 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.253-1223T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266062 | |||||||
| chr5:180266083 | T | C | 12 | a0001c0001t0004g0312 a0001c0001t0004g0313 a0001c0001t0004g0324 others(9): Show |
12 | HG00639.hp1 HG00642.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.253-1244A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266083 | |||||||
| chr5:180266113 | T | C | 1 | a0001c0001t0011g0197 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.253-1274A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266113 | |||||||
| chr5:180266150 | T | C | 1 | a0001c0001t0002g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.253-1311A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266150 | |||||||
| chr5:180266441 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.253-1602T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266441 | |||||||
| chr5:180266451 | A | G | 3 | a0001c0001t0003g0083 a0001c0001t0003g0095 a0001c0001t0003g0096 |
3 | HG01515.hp1 HG01517.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.253-1612T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266451 | |||||||
| chr5:180266530 | C | T | 13 | a0001c0001t0002g0080 a0001c0001t0002g0084 a0001c0001t0002g0086 others(10): Show |
14 | HG00280.hp2 HG02258.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.253-1691G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266530 | |||||||
| chr5:180266542 | C | T | 5 | a0001c0001t0001g0143 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | HG00558.hp1 HG02056.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-1703G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266542 | |||||||
| chr5:180266576 | C | A | 1 | a0001c0001t0001g0283 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.253-1737G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266576 | |||||||
| chr5:180266613 | C | T | 36 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0049 others(33): Show |
44 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.253-1774G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266613 | |||||||
| chr5:180266641 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.253-1802A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266641 | |||||||
| chr5:180266658 | G | T | 1 | a0001c0002t0012g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.253-1819C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266658 | |||||||
| chr5:180266820 | C | T | 8 | a0001c0001t0001g0150 a0001c0001t0001g0157 a0001c0001t0001g0159 others(5): Show |
8 | HG02135.hp2 HG02165.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.253-1981G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266820 | |||||||
| chr5:180266959 | C | T | 1 | a0001c0001t0005g0294 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.253-2120G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266959 | |||||||
| chr5:180266960 | G | T | 8 | a0001c0001t0002g0080 a0001c0001t0002g0086 a0001c0001t0002g0087 others(5): Show |
9 | HG00280.hp2 HG03490.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-2121C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266960 | |||||||
| chr5:180267062 | T | C | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.252+2218A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267062 | |||||||
| chr5:180267068 | G | A | 85 | a0001c0001t0002g0080 a0001c0001t0002g0084 a0001c0001t0002g0086 others(82): Show |
89 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.252+2212C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267068 | |||||||
| chr5:180267166 | A | G | 14 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0314 others(11): Show |
15 | HG00733.hp1 HG01074.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.252+2114T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267166 | |||||||
| chr5:180267178 | C | T | 12 | a0001c0001t0004g0312 a0001c0001t0004g0313 a0001c0001t0004g0324 others(9): Show |
12 | HG00639.hp1 HG00642.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.252+2102G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267178 | |||||||
| chr5:180267279 | A | G | 6 | a0001c0001t0001g0148 a0001c0001t0003g0088 a0001c0001t0003g0091 others(3): Show |
6 | HG00423.hp1 HG00673.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+2001T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267279 | |||||||
| chr5:180267283 | C | T | 40 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0126 others(37): Show |
43 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.252+1997G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267283 | |||||||
| chr5:180267289 | C | T | 3 | a0001c0001t0015g0025 a0001c0001t0032g0111 a0001c0001t0039g0242 |
3 | HG01884.hp1 HG01952.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.252+1991G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267289 | |||||||
| chr5:180267324 | C | G | 10 | a0001c0001t0004g0312 a0001c0001t0004g0313 a0001c0001t0004g0324 others(7): Show |
10 | HG00642.hp2 HG01109.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.252+1956G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267324 | |||||||
| chr5:180267328 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.252+1952C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267328 | |||||||
| chr5:180267343 | C | T | 1 | a0001c0001t0003g0071 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.252+1937G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267343 | |||||||
| chr5:180267357 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.252+1923G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267357 | |||||||
| chr5:180267384 | A | G | 3 | a0001c0001t0002g0110 a0001c0001t0002g0112 a0001c0001t0002g0113 |
3 | HG02886.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.252+1896T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267384 | |||||||
| chr5:180267387 | C | G | 5 | a0001c0001t0001g0140 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG00140.hp1 HG00280.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+1893G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267387 | |||||||
| chr5:180267388 | CT | C | 15 | a0001c0001t0003g0091 a0001c0001t0007g0013 a0001c0001t0007g0130 others(12): Show |
16 | HG00099.hp2 HG00673.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.252+1891delA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267388 | |||||||
| chr5:180267389 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.252+1891A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267389 | |||||||
| chr5:180267392 | C | G | 1 | a0001c0001t0003g0091 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.252+1888G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267392 | |||||||
| chr5:180267418 | T | C | 29 | a0001c0001t0001g0239 a0001c0001t0003g0044 a0001c0001t0004g0021 others(26): Show |
30 | HG00733.hp1 HG01074.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.252+1862A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267418 | |||||||
| chr5:180267422 | T | C | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1858A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267422 | |||||||
| chr5:180267430 | C | T | 1 | a0001c0001t0007g0219 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.252+1850G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267430 | |||||||
| chr5:180267431 | G | A | 241 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(238): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.252+1849C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267431 | |||||||
| chr5:180267435 | A | G | 36 | a0001c0001t0001g0150 a0001c0001t0001g0160 a0001c0001t0001g0162 others(33): Show |
38 | HG00099.hp2 HG00733.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.252+1845T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267435 | |||||||
| chr5:180267447 | G | A | 5 | a0001c0001t0016g0045 a0001c0001t0019g0215 a0001c0001t0019g0216 others(2): Show |
5 | HG01934.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+1833C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267447 | |||||||
| chr5:180267454 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.252+1826G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267454 | |||||||
| chr5:180267455 | G | A | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1825C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267455 | |||||||
| chr5:180267472 | G | A | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1808C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267472 | |||||||
| chr5:180267474 | A | G | 1 | a0001c0001t0041g0302 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.252+1806T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267474 | |||||||
| chr5:180267478 | C | T | 6 | a0001c0001t0004g0318 a0001c0001t0007g0223 a0001c0001t0007g0226 others(3): Show |
7 | HG03491.hp2 HG03492.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.252+1802G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267478 | |||||||
| chr5:180267486 | T | C | 15 | a0001c0001t0001g0150 a0001c0001t0001g0160 a0001c0001t0001g0162 others(12): Show |
15 | HG01884.hp1 HG02135.hp2 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.252+1794A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267486 | |||||||
| chr5:180267493 | C | T | 1 | a0001c0001t0014g0309 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.252+1787G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267493 | |||||||
| chr5:180267503 | A | G | 87 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(84): Show |
95 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.252+1777T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267503 | |||||||
| chr5:180267510 | T | C | 20 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0003g0119 others(17): Show |
26 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.252+1770A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267510 | |||||||
| chr5:180267516 | C | T | 3 | a0001c0001t0002g0049 a0001c0001t0002g0060 a0001c0001t0002g0082 |
3 | HG00741.hp1 HG01099.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.252+1764G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267516 | |||||||
| chr5:180267517 | G | A | 1 | a0001c0001t0031g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.252+1763C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267517 | |||||||
| chr5:180267519 | G | A | 3 | a0001c0001t0004g0315 a0001c0001t0004g0316 a0001c0001t0010g0047 |
3 | HG00639.hp2 NA19062.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.252+1761C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267519 | |||||||
| chr5:180267527 | C | A | 3 | a0001c0001t0002g0058 a0001c0001t0007g0132 a0001c0001t0010g0047 |
3 | HG00639.hp2 HG03831.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.252+1753G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267527 | |||||||
| chr5:180267534 | G | A | 1 | a0001c0001t0007g0132 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.252+1746C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267534 | |||||||
| chr5:180267534 | G | C | 1 | a0001c0001t0010g0047 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.252+1746C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267534 | |||||||
| chr5:180267535 | T | C | 2 | a0001c0001t0007g0132 a0001c0001t0010g0047 |
2 | HG00639.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.252+1745A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267535 | |||||||
| chr5:180267540 | C | A | 1 | a0001c0001t0010g0047 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.252+1740G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267540 | |||||||
| chr5:180267540 | C | T | 3 | a0001c0001t0001g0239 a0001c0001t0002g0118 a0001c0001t0007g0132 |
3 | HG03486.hp1 NA19002.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.252+1740G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267540 | |||||||
| chr5:180267548 | C | T | 1 | a0001c0001t0032g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.252+1732G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267548 | |||||||
| chr5:180267554 | T | A | 1 | a0001c0001t0007g0132 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.252+1726A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267554 | |||||||
| chr5:180267556 | C | T | 1 | a0001c0001t0005g0296 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.252+1724G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267556 | |||||||
| chr5:180267557 | G | A | 2 | a0001c0001t0024g0260 a0001c0001t0024g0261 |
2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.252+1723C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267557 | |||||||
| chr5:180267561 | C | CA | 8 | a0001c0001t0002g0055 a0001c0001t0002g0068 a0001c0001t0002g0113 others(5): Show |
8 | HG00741.hp2 HG01109.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+1718dupT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267561 | |||||||
| chr5:180267561 | CA | C | 188 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0125 others(185): Show |
201 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.252+1718delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267561 | |||||||
| chr5:180267561 | CAA | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(73): Show |
82 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.252+1717_252+1718d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267561 | |||||||
| chr5:180267599 | CATGCATT others(17): Show |
C | 1 | a0001c0001t0007g0221 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.252+1657_252+1680d others(26): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267599 | |||||||
| chr5:180267680 | G | T | 214 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(211): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.252+1600C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267680 | |||||||
| chr5:180267690 | C | G | 22 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0194 others(19): Show |
24 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.252+1590G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267690 | |||||||
| chr5:180267691 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.252+1589G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267691 | |||||||
| chr5:180267717 | C | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0126 others(71): Show |
80 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.252+1563G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267717 | |||||||
| chr5:180267734 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.252+1546C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267734 | |||||||
| chr5:180267760 | A | G | 138 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0152 others(135): Show |
144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.252+1520T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267760 | |||||||
| chr5:180267778 | T | C | 20 | a0001c0001t0001g0195 a0001c0001t0001g0210 a0001c0001t0001g0252 others(17): Show |
20 | HG01884.hp1 HG01952.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.252+1502A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267778 | |||||||
| chr5:180267805 | C | CTG | 3 | a0001c0001t0001g0187 a0001c0001t0001g0254 a0001c0001t0001g0256 |
3 | HG00673.hp2 HG02132.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.252+1473_252+1474d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267805 | |||||||
| chr5:180267808 | T | C | 1 | a0001c0001t0004g0332 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.252+1472A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267808 | |||||||
| chr5:180267809 | C | G | 3 | a0001c0001t0002g0049 a0001c0001t0004g0318 a0001c0001t0030g0064 |
3 | HG01099.hp2 HG02165.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.252+1471G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267809 | |||||||
| chr5:180267811 | CA | C | 116 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0019 others(113): Show |
123 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.252+1468delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267811 | |||||||
| chr5:180267812 | A | C | 2 | a0001c0001t0004g0318 a0001c0001t0030g0064 |
2 | HG02165.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.252+1468T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267812 | |||||||
| chr5:180267824 | C | CA | 7 | a0001c0001t0001g0169 a0001c0001t0007g0134 a0001c0001t0007g0226 others(4): Show |
7 | HG00099.hp2 HG01884.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+1455dupT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267824 | |||||||
| chr5:180267824 | CA | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0248 a0001c0001t0001g0249 others(7): Show |
11 | HG01515.hp2 HG02280.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.252+1455delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267824 | |||||||
| chr5:180267833 | C | A | 2 | a0001c0001t0006g0032 a0001c0001t0044g0340 |
2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.252+1447G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267833 | |||||||
| chr5:180267852 | TTTTA | T | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0006g0027 others(1): Show |
4 | HG01243.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1424_252+1427d others(6): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267852 | |||||||
| chr5:180267932 | A | G | 12 | a0001c0001t0001g0174 a0001c0001t0002g0114 a0001c0001t0002g0115 others(9): Show |
12 | HG01952.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.252+1348T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267932 | |||||||
| chr5:180267948 | T | C | 4 | a0001c0001t0002g0054 a0001c0001t0002g0069 a0001c0001t0022g0343 others(1): Show |
4 | HG01884.hp2 HG02015.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+1332A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267948 | |||||||
| chr5:180267949 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.252+1331C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267949 | |||||||
| chr5:180267963 | T | C | 6 | a0001c0001t0001g0138 a0001c0001t0021g0263 a0001c0001t0022g0341 others(3): Show |
6 | HG02258.hp1 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+1317A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267963 | |||||||
| chr5:180267964 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.252+1316C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267964 | |||||||
| chr5:180267975 | A | G | 14 | a0001c0001t0005g0306 a0001c0001t0007g0013 a0001c0001t0007g0130 others(11): Show |
15 | HG01975.hp2 HG02155.hp2 HG03239.hp2 others(12): Show |
intron_variant | MODIFIER | c.252+1305T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267975 | |||||||
| chr5:180268000 | C | T | 5 | a0001c0001t0001g0171 a0001c0001t0021g0262 a0001c0001t0021g0263 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+1280G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268000 | |||||||
| chr5:180268014 | T | C | 1 | a0001c0001t0031g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.252+1266A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268014 | |||||||
| chr5:180268021 | T | G | 4 | a0001c0001t0007g0130 a0001c0001t0007g0131 a0001c0001t0007g0132 others(1): Show |
4 | HG02155.hp2 NA19002.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1259A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268021 | |||||||
| chr5:180268026 | A | G | 4 | a0001c0001t0007g0130 a0001c0001t0007g0131 a0001c0001t0007g0132 others(1): Show |
4 | HG02155.hp2 NA19002.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1254T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268026 | |||||||
| chr5:180268046 | T | G | 41 | a0001c0001t0001g0147 a0001c0001t0002g0001 a0001c0001t0002g0009 others(38): Show |
46 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.252+1234A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268046 | |||||||
| chr5:180268054 | G | A | 1 | a0001c0002t0012g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.252+1226C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268054 | |||||||
| chr5:180268057 | G | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(38): Show |
45 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.252+1223C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268057 | |||||||
| chr5:180268069 | C | G | 1 | a0001c0001t0006g0039 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.252+1211G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268069 | |||||||
| chr5:180268076 | G | A | 42 | a0001c0001t0001g0140 a0001c0001t0001g0144 a0001c0001t0001g0146 others(39): Show |
42 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.252+1204C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268076 | |||||||
| chr5:180268083 | T | C | 23 | a0001c0001t0001g0269 a0001c0001t0002g0001 a0001c0001t0002g0050 others(20): Show |
27 | HG00099.hp2 HG01192.hp2 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.252+1197A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268083 | |||||||
| chr5:180268113 | T | C | 111 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0126 others(108): Show |
127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.252+1167A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268113 | |||||||
| chr5:180268116 | A | G | 43 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0126 others(40): Show |
47 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.252+1164T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268116 | |||||||
| chr5:180268352 | C | G | 251 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(248): Show |
269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.252+928G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268352 | |||||||
| chr5:180268368 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.252+912G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268368 | |||||||
| chr5:180268430 | T | C | 90 | a0001c0001t0001g0019 a0001c0001t0001g0157 a0001c0001t0001g0236 others(87): Show |
95 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.252+850A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268430 | |||||||
| chr5:180268436 | C | T | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+844G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268436 | |||||||
| chr5:180268447 | T | C | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.252+833A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268447 | |||||||
| chr5:180268485 | T | A | 19 | a0001c0001t0001g0020 a0001c0001t0001g0209 a0001c0001t0001g0239 others(16): Show |
20 | HG00609.hp2 HG00642.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.252+795A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268485 | |||||||
| chr5:180268550 | G | A | 6 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+730C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268550 | |||||||
| chr5:180268566 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.252+714C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268566 | |||||||
| chr5:180268603 | G | A | 1 | a0001c0001t0012g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.252+677C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268603 | |||||||
| chr5:180268610 | G | A | 2 | a0001c0001t0011g0198 a0001c0001t0011g0199 |
2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.252+670C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268610 | |||||||
| chr5:180268617 | G | A | 1 | a0001c0001t0005g0304 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.252+663C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268617 | |||||||
| chr5:180268642 | G | A | 4 | a0001c0001t0002g0110 a0001c0001t0002g0112 a0001c0001t0002g0113 others(1): Show |
4 | HG02258.hp1 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+638C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268642 | |||||||
| chr5:180268643 | C | T | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.252+637G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268643 | |||||||
| chr5:180268688 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.252+592C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268688 | |||||||
| chr5:180268814 | G | A | 45 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(42): Show |
50 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.252+466C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268814 | |||||||
| chr5:180268949 | C | G | 1 | a0001c0001t0002g0078 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.252+331G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268949 | |||||||
| chr5:180269088 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.252+192C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180269088 | |||||||
| chr5:180269095 | C | T | 1 | a0001c0001t0018g0123 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.252+185G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180269095 | |||||||
| chr5:180269128 | C | A | 1 | a0001c0001t0001g0184 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.252+152G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180269128 | |||||||
| chr5:180269446 | C | T | 1 | a0001c0001t0004g0325 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.123-37G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180269446 | |||||||
| chr5:180269583 | C | A | 1 | a0001c0001t0013g0247 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.123-174G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180269583 | |||||||
| chr5:180269821 | A | T | 1 | a0001c0001t0001g0268 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.123-412T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180269821 | |||||||
| chr5:180269872 | T | C | 1 | a0001c0001t0025g0213 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.123-463A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180269872 | |||||||
| chr5:180269976 | C | A | 13 | a0001c0001t0002g0080 a0001c0001t0003g0071 a0001c0001t0008g0003 others(10): Show |
17 | HG00733.hp2 HG00741.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-567G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180269976 | |||||||
| chr5:180269997 | A | C | 11 | a0001c0001t0008g0046 a0001c0001t0020g0204 a0001c0001t0020g0228 others(8): Show |
11 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.123-588T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180269997 | |||||||
| chr5:180269997 | A | G | 85 | a0001c0001t0001g0019 a0001c0001t0001g0207 a0001c0001t0001g0210 others(82): Show |
90 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.123-588T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180269997 | |||||||
| chr5:180270230 | C | A | 4 | a0001c0001t0004g0324 a0001c0001t0004g0329 a0001c0001t0004g0330 others(1): Show |
4 | HG00642.hp2 HG01109.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-821G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270230 | |||||||
| chr5:180270502 | T | C | 94 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0125 others(91): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.123-1093A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270502 | |||||||
| chr5:180270516 | G | A | 2 | a0001c0001t0017g0154 a0001c0001t0017g0155 |
2 | HG01243.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.123-1107C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270516 | |||||||
| chr5:180270535 | C | T | 154 | a0001c0001t0001g0019 a0001c0001t0001g0207 a0001c0001t0001g0210 others(151): Show |
168 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.123-1126G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270535 | |||||||
| chr5:180270542 | C | G | 2 | a0001c0001t0004g0312 a0001c0001t0004g0313 |
2 | HG01934.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.123-1133G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270542 | |||||||
| chr5:180270543 | T | G | 1 | a0001c0001t0005g0303 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.123-1134A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270543 | |||||||
| chr5:180270827 | T | A | 2 | a0001c0001t0002g0055 a0001c0001t0002g0077 |
2 | HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.123-1418A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270827 | |||||||
| chr5:180270858 | C | CA | 35 | a0001c0001t0001g0170 a0001c0001t0001g0184 a0001c0001t0001g0201 others(32): Show |
36 | HG00423.hp1 HG00544.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.123-1450dupT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270858 | |||||||
| chr5:180270858 | C | CAA | 15 | a0001c0001t0001g0185 a0001c0001t0001g0193 a0001c0001t0001g0202 others(12): Show |
15 | HG01884.hp2 HG01978.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.123-1451_123-1450d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270858 | |||||||
| chr5:180270861 | AAAAAAAA others(12): Show |
A | 6 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0021g0262 others(3): Show |
6 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-1471_123-1453d others(21): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270861 | |||||||
| chr5:180270868 | A | AAAAAAAG | 8 | a0001c0001t0006g0006 a0001c0001t0006g0027 a0001c0001t0006g0029 others(5): Show |
9 | HG01167.hp2 HG01243.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-1460_123-1459i others(9): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270868 | |||||||
| chr5:180270868 | A | AAAAAAG | 11 | a0001c0001t0006g0028 a0001c0001t0006g0035 a0001c0001t0006g0036 others(8): Show |
12 | HG02055.hp2 HG02071.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.123-1465_123-1460d others(8): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270868 | |||||||
| chr5:180270873 | A | G | 1 | a0001c0001t0016g0120 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123-1464T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270873 | |||||||
| chr5:180270873 | AG | A | 42 | a0001c0001t0001g0019 a0001c0001t0001g0248 a0001c0001t0001g0249 others(39): Show |
50 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.123-1465delC | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270873 | |||||||
| chr5:180270874 | G | A | 112 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(109): Show |
116 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.123-1465C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270874 | |||||||
| chr5:180270880 | G | A | 1 | a0001c0001t0004g0314 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.123-1471C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270880 | |||||||
| chr5:180270881 | A | C | 1 | a0001c0001t0007g0221 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.123-1472T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270881 | |||||||
| chr5:180270907 | G | C | 1 | a0001c0001t0003g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.123-1498C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270907 | |||||||
| chr5:180271036 | TGA | T | 5 | a0001c0001t0011g0218 a0001c0001t0023g0121 a0001c0001t0023g0122 others(2): Show |
5 | HG02145.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-1629_123-1628d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271036 | |||||||
| chr5:180271187 | TA | T | 5 | a0001c0001t0011g0218 a0001c0001t0023g0121 a0001c0001t0023g0122 others(2): Show |
5 | HG02145.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-1779delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271187 | |||||||
| chr5:180271391 | C | A | 1 | a0001c0001t0012g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.123-1982G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271391 | |||||||
| chr5:180271442 | C | T | 5 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(2): Show |
5 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-2033G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271442 | |||||||
| chr5:180271554 | C | T | 152 | a0001c0001t0001g0019 a0001c0001t0001g0207 a0001c0001t0001g0210 others(149): Show |
166 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.123-2145G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271554 | |||||||
| chr5:180271611 | G | A | 1 | a0001c0001t0012g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.123-2202C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271611 | |||||||
| chr5:180271619 | T | C | 5 | a0001c0001t0005g0298 a0001c0001t0005g0299 a0001c0001t0005g0300 others(2): Show |
5 | HG00438.hp1 NA18969.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-2210A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271619 | |||||||
| chr5:180271848 | T | G | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-2439A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271848 | |||||||
| chr5:180271890 | T | C | 43 | a0001c0001t0001g0125 a0001c0001t0001g0140 a0001c0001t0001g0144 others(40): Show |
43 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.123-2481A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271890 | |||||||
| chr5:180272012 | A | ACTCCACA others(71): Show |
1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.123-2681_123-2604d others(80): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272012 | |||||||
| chr5:180272112 | T | A | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.123-2703A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272112 | |||||||
| chr5:180272125 | T | C | 41 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0049 others(38): Show |
49 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.123-2716A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272125 | |||||||
| chr5:180272198 | CTT | C | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-2791_123-2790d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272198 | |||||||
| chr5:180272267 | T | C | 1 | a0001c0001t0020g0230 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.123-2858A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272267 | |||||||
| chr5:180272420 | C | T | 1 | a0001c0001t0013g0247 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.123-3011G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272420 | |||||||
| chr5:180272504 | G | C | 205 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0207 others(202): Show |
222 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.123-3095C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272504 | |||||||
| chr5:180272686 | A | G | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-3277T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272686 | |||||||
| chr5:180272911 | G | A | 332 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(329): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.123-3502C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272911 | |||||||
| chr5:180273153 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.123-3744A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273153 | |||||||
| chr5:180273215 | ATCTT | A | 41 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0049 others(38): Show |
49 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.123-3810_123-3807d others(6): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273215 | |||||||
| chr5:180273464 | C | T | 2 | a0001c0001t0012g0240 a0001c0001t0012g0241 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.123-4055G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273464 | |||||||
| chr5:180273503 | A | G | 1 | a0001c0001t0002g0055 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.123-4094T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273503 | |||||||
| chr5:180273603 | T | C | 129 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0207 others(126): Show |
137 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.123-4194A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273603 | |||||||
| chr5:180273621 | G | A | 9 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0012g0240 others(6): Show |
9 | HG01952.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-4212C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273621 | |||||||
| chr5:180273673 | A | G | 1 | a0001c0001t0039g0242 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.123-4264T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273673 | |||||||
| chr5:180273777 | A | G | 41 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0049 others(38): Show |
49 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.123-4368T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273777 | |||||||
| chr5:180273983 | C | CT | 58 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(55): Show |
63 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.123-4575dupA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273983 | |||||||
| chr5:180274001 | C | T | 1 | a0001c0001t0006g0026 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.123-4592G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274001 | |||||||
| chr5:180274341 | C | T | 3 | a0001c0001t0012g0206 a0001c0002t0012g0245 a0001c0002t0012g0246 |
3 | HG02145.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.123-4932G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274341 | |||||||
| chr5:180274397 | C | T | 5 | a0001c0001t0011g0218 a0001c0001t0023g0121 a0001c0001t0023g0122 others(2): Show |
5 | HG02145.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-4988G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274397 | |||||||
| chr5:180274502 | C | T | 27 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(24): Show |
28 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.123-5093G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274502 | |||||||
| chr5:180274516 | G | A | 1 | a0001c0001t0011g0218 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.123-5107C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274516 | |||||||
| chr5:180274641 | C | CA | 3 | a0001c0001t0012g0206 a0001c0002t0012g0245 a0001c0002t0012g0246 |
3 | HG02145.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.123-5233dupT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274641 | |||||||
| chr5:180274753 | A | G | 28 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(25): Show |
29 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-5344T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274753 | |||||||
| chr5:180274762 | T | C | 5 | a0001c0001t0011g0218 a0001c0001t0023g0121 a0001c0001t0023g0122 others(2): Show |
5 | HG02145.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-5353A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274762 | |||||||
| chr5:180275122 | T | C | 5 | a0001c0001t0011g0218 a0001c0001t0023g0121 a0001c0001t0023g0122 others(2): Show |
5 | HG02145.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+5318A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275122 | |||||||
| chr5:180275198 | C | T | 2 | a0001c0001t0001g0254 a0001c0001t0001g0256 |
2 | HG00673.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.122+5242G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275198 | |||||||
| chr5:180275332 | C | T | 1 | a0001c0001t0017g0014 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.122+5108G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275332 | |||||||
| chr5:180275631 | C | A | 3 | a0001c0001t0005g0292 a0001c0001t0015g0022 a0001c0001t0015g0023 |
3 | HG02055.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.122+4809G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275631 | |||||||
| chr5:180275749 | C | T | 1 | a0001c0001t0032g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.122+4691G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275749 | |||||||
| chr5:180275797 | T | C | 9 | a0001c0001t0001g0152 a0001c0001t0001g0186 a0001c0001t0001g0187 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+4643A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275797 | |||||||
| chr5:180275890 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.122+4550G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275890 | |||||||
| chr5:180275980 | CTTAAATG others(7): Show |
C | 3 | a0001c0001t0006g0035 a0001c0001t0006g0039 a0001c0001t0006g0040 |
3 | NA18956.hp1 NA18972.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.122+4446_122+4459d others(16): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275980 | |||||||
| chr5:180275986 | T | C | 1 | a0001c0001t0006g0032 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.122+4454A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275986 | |||||||
| chr5:180276098 | C | T | 18 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(15): Show |
19 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.122+4342G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276098 | |||||||
| chr5:180276219 | A | G | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.122+4221T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276219 | |||||||
| chr5:180276221 | G | A | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+4219C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276221 | |||||||
| chr5:180276257 | G | A | 1 | a0001c0001t0009g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.122+4183C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276257 | |||||||
| chr5:180276413 | C | T | 5 | a0001c0001t0011g0218 a0001c0001t0023g0121 a0001c0001t0023g0122 others(2): Show |
5 | HG02145.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+4027G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276413 | |||||||
| chr5:180276458 | A | C | 1 | a0001c0001t0001g0195 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.122+3982T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276458 | |||||||
| chr5:180276709 | C | A | 3 | a0001c0001t0008g0003 a0001c0001t0008g0011 a0001c0001t0008g0081 |
6 | HG01071.hp1 HG01261.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+3731G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276709 | |||||||
| chr5:180276724 | C | T | 1 | a0001c0001t0003g0085 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.122+3716G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276724 | |||||||
| chr5:180276847 | G | A | 2 | a0001c0001t0014g0309 a0001c0001t0014g0310 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.122+3593C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276847 | |||||||
| chr5:180276926 | A | G | 2 | a0001c0001t0017g0154 a0001c0001t0017g0155 |
2 | HG01243.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.122+3514T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276926 | |||||||
| chr5:180276930 | CAAAT | C | 18 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(15): Show |
19 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.122+3506_122+3509d others(6): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276930 | |||||||
| chr5:180276972 | T | G | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+3468A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276972 | |||||||
| chr5:180277020 | G | A | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+3420C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277020 | |||||||
| chr5:180277032 | G | A | 18 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(15): Show |
19 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.122+3408C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277032 | |||||||
| chr5:180277214 | G | T | 1 | a0001c0001t0013g0247 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.122+3226C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277214 | |||||||
| chr5:180277230 | A | G | 3 | a0001c0001t0007g0130 a0001c0001t0007g0131 a0001c0001t0007g0135 |
3 | HG02155.hp2 NA19054.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.122+3210T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277230 | |||||||
| chr5:180277255 | G | A | 8 | a0001c0001t0008g0046 a0001c0001t0020g0204 a0001c0001t0020g0228 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+3185C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277255 | |||||||
| chr5:180277523 | G | A | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.122+2917C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277523 | |||||||
| chr5:180277542 | T | C | 1 | a0001c0001t0045g0344 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.122+2898A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277542 | |||||||
| chr5:180277576 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0101 a0001c0001t0012g0206 |
5 | HG01928.hp1 HG01952.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+2864C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277576 | |||||||
| chr5:180277627 | T | C | 58 | a0001c0001t0001g0019 a0001c0001t0001g0236 a0001c0001t0001g0237 others(55): Show |
63 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.122+2813A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277627 | |||||||
| chr5:180277651 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.122+2789G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277651 | |||||||
| chr5:180277712 | C | T | 19 | a0001c0001t0001g0005 a0001c0001t0007g0013 a0001c0001t0007g0130 others(16): Show |
22 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(19): Show |
intron_variant | MODIFIER | c.122+2728G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277712 | |||||||
| chr5:180277740 | T | C | 19 | a0001c0001t0001g0020 a0001c0001t0001g0209 a0001c0001t0001g0239 others(16): Show |
20 | HG00609.hp2 HG00642.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.122+2700A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277740 | |||||||
| chr5:180277758 | C | A | 1 | a0001c0001t0006g0033 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122+2682G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277758 | |||||||
| chr5:180277761 | C | T | 1 | a0001c0001t0008g0079 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.122+2679G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277761 | |||||||
| chr5:180277809 | C | T | 11 | a0001c0001t0008g0046 a0001c0001t0020g0204 a0001c0001t0020g0228 others(8): Show |
11 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.122+2631G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277809 | |||||||
| chr5:180277903 | C | T | 33 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(30): Show |
34 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.122+2537G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277903 | |||||||
| chr5:180278182 | C | A | 1 | a0001c0001t0001g0255 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.122+2258G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278182 | |||||||
| chr5:180278265 | T | G | 1 | a0001c0001t0012g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.122+2175A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278265 | |||||||
| chr5:180278312 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.122+2128A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278312 | |||||||
| chr5:180278398 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.122+2042C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278398 | |||||||
| chr5:180278424 | G | A | 1 | a0001c0001t0012g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.122+2016C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278424 | |||||||
| chr5:180278646 | C | A | 28 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(25): Show |
29 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+1794G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278646 | |||||||
| chr5:180278653 | C | T | 18 | a0001c0001t0007g0013 a0001c0001t0007g0130 a0001c0001t0007g0131 others(15): Show |
19 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.122+1787G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278653 | |||||||
| chr5:180278655 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.122+1785G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278655 | |||||||
| chr5:180278785 | CCT | C | 29 | a0001c0001t0001g0210 a0001c0001t0004g0021 a0001c0001t0004g0286 others(26): Show |
30 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.122+1653_122+1654d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278785 | |||||||
| chr5:180278812 | G | A | 1 | a0001c0001t0006g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.122+1628C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278812 | |||||||
| chr5:180278955 | A | C | 5 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(2): Show |
5 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+1485T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278955 | |||||||
| chr5:180278957 | C | CT | 27 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(24): Show |
27 | HG01175.hp1 HG01952.hp2 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.122+1482dupA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278957 | |||||||
| chr5:180278970 | T | C | 48 | a0001c0001t0001g0020 a0001c0001t0001g0209 a0001c0001t0001g0239 others(45): Show |
51 | HG00609.hp2 HG00642.hp1 HG01167.hp2 others(48): Show |
intron_variant | MODIFIER | c.122+1470A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278970 | |||||||
| chr5:180279019 | G | A | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+1421C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279019 | |||||||
| chr5:180279025 | T | C | 5 | a0001c0001t0011g0218 a0001c0001t0023g0121 a0001c0001t0023g0122 others(2): Show |
5 | HG02145.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+1415A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279025 | |||||||
| chr5:180279099 | G | A | 20 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(17): Show |
22 | HG01167.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.122+1341C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279099 | |||||||
| chr5:180279156 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.122+1284G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279156 | |||||||
| chr5:180279247 | T | C | 205 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0207 others(202): Show |
222 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.122+1193A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279247 | |||||||
| chr5:180279367 | G | C | 1 | a0001c0001t0008g0079 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.122+1073C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279367 | |||||||
| chr5:180279395 | A | C | 6 | a0001c0001t0001g0125 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
6 | HG00558.hp2 HG00621.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+1045T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279395 | |||||||
| chr5:180279705 | GA | G | 28 | a0001c0001t0004g0021 a0001c0001t0004g0286 a0001c0001t0004g0312 others(25): Show |
29 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+734delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279705 | |||||||
| chr5:180279829 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.122+611G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279829 | |||||||
| chr5:180279846 | G | C | 1 | a0001c0001t0025g0284 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.122+594C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279846 | |||||||
| chr5:180279892 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.122+548T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279892 | |||||||
| chr5:180280194 | G | A | 202 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0207 others(199): Show |
219 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.122+246C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180280194 | |||||||
| chr5:180280254 | G | A | 1 | a0001c0001t0014g0311 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.122+186C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180280254 | |||||||
| chr5:180280339 | T | A | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+101A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180280339 | |||||||
| chr5:180280394 | T | C | 21 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(18): Show |
23 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.122+46A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180280394 | |||||||
| chr5:180280657 | G | A | 1 | a0001c0001t0032g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-47-49C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180280657 | |||||||
| chr5:180280920 | C | T | 2 | a0001c0001t0007g0219 a0001c0001t0007g0220 |
2 | HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-47-312G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180280920 | |||||||
| chr5:180280991 | G | A | 1 | a0001c0001t0007g0135 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-47-383C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180280991 | |||||||
| chr5:180281065 | T | A | 21 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(18): Show |
23 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-47-457A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281065 | |||||||
| chr5:180281186 | A | T | 1 | a0001c0001t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47-578T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281186 | |||||||
| chr5:180281372 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0128 a0001c0001t0001g0194 others(1): Show |
5 | HG02155.hp1 NA18747.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-764A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281372 | |||||||
| chr5:180281442 | T | C | 1 | a0001c0001t0010g0103 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-47-834A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281442 | |||||||
| chr5:180281506 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-47-898A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281506 | |||||||
| chr5:180281564 | G | A | 6 | a0001c0001t0001g0205 a0001c0001t0008g0046 a0001c0001t0020g0204 others(3): Show |
6 | HG02572.hp1 HG03927.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-956C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281564 | |||||||
| chr5:180281896 | C | T | 40 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0050 others(37): Show |
48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-47-1288G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281896 | |||||||
| chr5:180281897 | G | A | 1 | a0001c0001t0004g0021 | 2 | HG00733.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-47-1289C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281897 | |||||||
| chr5:180282049 | C | A | 1 | a0001c0001t0008g0011 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-47-1441G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282049 | |||||||
| chr5:180282154 | T | C | 239 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(236): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.-47-1546A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282154 | |||||||
| chr5:180282194 | A | G | 2 | a0001c0001t0010g0012 a0001c0001t0010g0107 |
3 | HG03491.hp2 HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-47-1586T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282194 | |||||||
| chr5:180282235 | C | T | 3 | a0001c0001t0005g0292 a0001c0001t0026g0291 a0001c0001t0026g0293 |
3 | HG02647.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-47-1627G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282235 | |||||||
| chr5:180282267 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-47-1659C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282267 | |||||||
| chr5:180282268 | C | G | 1 | a0001c0001t0002g0054 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-47-1660G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282268 | |||||||
| chr5:180282282 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-47-1674G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282282 | |||||||
| chr5:180282295 | G | A | 6 | a0001c0001t0001g0205 a0001c0001t0008g0046 a0001c0001t0020g0204 others(3): Show |
6 | HG02572.hp1 HG03927.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-1687C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282295 | |||||||
| chr5:180282318 | G | T | 1 | a0001c0001t0015g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47-1710C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282318 | |||||||
| chr5:180282400 | C | T | 40 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0050 others(37): Show |
48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-47-1792G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282400 | |||||||
| chr5:180282481 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-47-1873T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282481 | |||||||
| chr5:180282528 | A | C | 195 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(192): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-47-1920T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282528 | |||||||
| chr5:180282528 | A | T | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-1920T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282528 | |||||||
| chr5:180282544 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-47-1936G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282544 | |||||||
| chr5:180282560 | T | C | 1 | a0001c0001t0006g0041 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-47-1952A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282560 | |||||||
| chr5:180282589 | C | A | 90 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0209 others(87): Show |
96 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-47-1981G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282589 | |||||||
| chr5:180282731 | C | T | 15 | a0001c0001t0002g0049 a0001c0001t0004g0021 a0001c0001t0004g0286 others(12): Show |
16 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.-47-2123G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282731 | |||||||
| chr5:180282922 | G | A | 4 | a0001c0001t0011g0196 a0001c0001t0011g0197 a0001c0001t0011g0198 others(1): Show |
4 | HG01192.hp1 HG03710.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-2314C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282922 | |||||||
| chr5:180282923 | G | C | 5 | a0001c0001t0018g0123 a0001c0001t0018g0124 a0001c0001t0018g0211 others(2): Show |
5 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-2315C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282923 | |||||||
| chr5:180282926 | G | A | 90 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0209 others(87): Show |
96 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-47-2318C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282926 | |||||||
| chr5:180282968 | G | A | 3 | a0001c0001t0012g0206 a0001c0002t0012g0245 a0001c0002t0012g0246 |
3 | HG02145.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-47-2360C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282968 | |||||||
| chr5:180283039 | C | T | 2 | a0001c0001t0004g0312 a0001c0001t0004g0313 |
2 | HG01934.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-47-2431G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283039 | |||||||
| chr5:180283087 | C | T | 1 | a0001c0001t0045g0344 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-47-2479G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283087 | |||||||
| chr5:180283194 | G | A | 40 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0050 others(37): Show |
48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-47-2586C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283194 | |||||||
| chr5:180283502 | C | T | 40 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0050 others(37): Show |
48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-47-2894G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283502 | |||||||
| chr5:180283663 | T | C | 40 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0050 others(37): Show |
48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-47-3055A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283663 | |||||||
| chr5:180283675 | C | T | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-3067G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283675 | |||||||
| chr5:180283889 | C | A | 7 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(4): Show |
7 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47-3281G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283889 | |||||||
| chr5:180283897 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-47-3289A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283897 | |||||||
| chr5:180283915 | G | A | 72 | a0001c0001t0001g0019 a0001c0001t0001g0236 a0001c0001t0001g0237 others(69): Show |
77 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-47-3307C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283915 | |||||||
| chr5:180283922 | C | T | 28 | a0001c0001t0002g0049 a0001c0001t0004g0021 a0001c0001t0004g0286 others(25): Show |
29 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-47-3314G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283922 | |||||||
| chr5:180284032 | C | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0248 a0001c0001t0001g0249 |
4 | HG02896.hp1 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-3424G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284032 | |||||||
| chr5:180284184 | C | T | 119 | a0001c0001t0001g0019 a0001c0001t0001g0207 a0001c0001t0001g0210 others(116): Show |
125 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-47-3576G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284184 | |||||||
| chr5:180284186 | A | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0248 a0001c0001t0001g0249 |
4 | HG02896.hp1 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-3578T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284186 | |||||||
| chr5:180284289 | C | A | 64 | a0001c0001t0001g0019 a0001c0001t0001g0236 a0001c0001t0001g0237 others(61): Show |
69 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.-47-3681G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284289 | |||||||
| chr5:180284502 | G | A | 1 | a0001c0001t0010g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-47-3894C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284502 | |||||||
| chr5:180284561 | A | C | 1 | a0001c0001t0002g0110 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-47-3953T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284561 | |||||||
| chr5:180284663 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-47-4055A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284663 | |||||||
| chr5:180284692 | AT | A | 6 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-4085delA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284692 | |||||||
| chr5:180284695 | T | G | 6 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-4087A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284695 | |||||||
| chr5:180284862 | C | T | 1 | a0001c0001t0038g0136 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-47-4254G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284862 | |||||||
| chr5:180284898 | G | A | 93 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0125 others(90): Show |
96 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.-47-4290C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284898 | |||||||
| chr5:180284913 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-47-4305G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284913 | |||||||
| chr5:180284914 | G | A | 21 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(18): Show |
23 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-47-4306C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284914 | |||||||
| chr5:180284954 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-47-4346A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284954 | |||||||
| chr5:180285060 | A | G | 48 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0002g0049 others(45): Show |
49 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.-47-4452T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285060 | |||||||
| chr5:180285192 | T | G | 7 | a0001c0001t0014g0307 a0001c0001t0014g0308 a0001c0001t0014g0309 others(4): Show |
7 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47-4584A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285192 | |||||||
| chr5:180285194 | C | T | 2 | a0001c0001t0002g0114 a0001c0001t0002g0115 |
2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-47-4586G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285194 | |||||||
| chr5:180285451 | C | T | 19 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0011g0218 others(16): Show |
19 | HG01099.hp1 HG01928.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.-47-4843G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285451 | |||||||
| chr5:180285458 | G | A | 4 | a0001c0001t0019g0214 a0001c0001t0019g0215 a0001c0001t0019g0216 others(1): Show |
4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-4850C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285458 | |||||||
| chr5:180285650 | A | G | 1 | a0001c0001t0012g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-47-5042T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285650 | |||||||
| chr5:180285689 | G | A | 2 | a0001c0001t0002g0106 a0001c0001t0021g0253 |
2 | HG03490.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-47-5081C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285689 | |||||||
| chr5:180285719 | T | C | 3 | a0001c0001t0022g0341 a0001c0001t0022g0342 a0001c0001t0022g0343 |
3 | HG01884.hp2 HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-47-5111A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285719 | |||||||
| chr5:180285740 | A | G | 21 | a0001c0001t0006g0006 a0001c0001t0006g0026 a0001c0001t0006g0027 others(18): Show |
23 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-47-5132T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285740 | |||||||
| chr5:180285754 | A | T | 239 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(236): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.-47-5146T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285754 | |||||||
| chr5:180285767 | CAAT | C | 178 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0207 others(175): Show |
193 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.-47-5162_-47-5160d others(5): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285767 | |||||||
| chr5:180285817 | A | G | 1 | a0001c0001t0026g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5209T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285817 | |||||||
| chr5:180285846 | T | A | 1 | a0001c0001t0026g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5238A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285846 | |||||||
| chr5:180285848 | G | C | 1 | a0001c0001t0045g0344 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-47-5240C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285848 | |||||||
| chr5:180285850 | G | A | 29 | a0001c0001t0002g0049 a0001c0001t0004g0021 a0001c0001t0004g0286 others(26): Show |
30 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-47-5242C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285850 | |||||||
| chr5:180285851 | T | G | 1 | a0001c0001t0026g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5243A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285851 | |||||||
| chr5:180285853 | T | C | 1 | a0001c0001t0026g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5245A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285853 | |||||||
| chr5:180285860 | C | T | 1 | a0001c0001t0026g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5252G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285860 | |||||||
| chr5:180285861 | G | A | 1 | a0001c0001t0026g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5253C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285861 | |||||||
| chr5:180285873 | C | T | 1 | a0001c0001t0026g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5265G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285873 | |||||||
| chr5:180285874 | G | C | 1 | a0001c0001t0026g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5266C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285874 | |||||||
| chr5:180285894 | T | C | 3 | a0001c0001t0026g0293 a0001c0002t0012g0245 a0001c0002t0012g0246 |
3 | HG02630.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-47-5286A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285894 | |||||||
| chr5:180285895 | G | A | 1 | a0001c0001t0026g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5287C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285895 | |||||||
| chr5:180285903 | T | C | 1 | a0001c0001t0026g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5295A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285903 | |||||||
| chr5:180285906 | G | A | 1 | a0001c0001t0026g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5298C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285906 | |||||||
| chr5:180285936 | C | T | 1 | a0001c0001t0026g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5328G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285936 | |||||||
| chr5:180285944 | G | C | 1 | a0001c0001t0026g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5336C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285944 | |||||||
| chr5:180286075 | G | A | 1 | a0001c0001t0010g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-47-5467C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286075 | |||||||
| chr5:180286079 | CA | C | 177 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0207 others(174): Show |
192 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.-47-5472delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286079 | |||||||
| chr5:180286112 | T | C | 10 | a0001c0001t0001g0205 a0001c0001t0008g0046 a0001c0001t0020g0204 others(7): Show |
10 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47-5504A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286112 | |||||||
| chr5:180286145 | TTTCTTTT others(571): Show |
T | 18 | a0001c0001t0001g0020 a0001c0001t0001g0209 a0001c0001t0001g0239 others(15): Show |
19 | HG00609.hp2 HG00642.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-48+5125_-47-5538d others(2): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286145 | |||||||
| chr5:180286148 | C | CT | 124 | a0001c0001t0001g0019 a0001c0001t0001g0207 a0001c0001t0001g0210 others(121): Show |
132 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-47-5541dupA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286148 | |||||||
| chr5:180286177 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0165 a0001c0001t0001g0168 |
3 | HG01516.hp2 NA20129.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-47-5569C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286177 | |||||||
| chr5:180286304 | C | T | 3 | a0001c0001t0012g0206 a0001c0002t0012g0245 a0001c0002t0012g0246 |
3 | HG02145.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-48+5544G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286304 | |||||||
| chr5:180286366 | G | A | 6 | a0001c0001t0003g0088 a0001c0001t0003g0091 a0001c0001t0003g0092 others(3): Show |
6 | HG00438.hp2 HG00673.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+5482C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286366 | |||||||
| chr5:180286374 | G | A | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-48+5474C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286374 | |||||||
| chr5:180286493 | T | C | 29 | a0001c0001t0002g0049 a0001c0001t0004g0021 a0001c0001t0004g0286 others(26): Show |
30 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-48+5355A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286493 | |||||||
| chr5:180286635 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-48+5213C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286635 | |||||||
| chr5:180286654 | G | A | 1 | a0001c0001t0045g0344 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-48+5194C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286654 | |||||||
| chr5:180286719 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-48+5129C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286719 | |||||||
| chr5:180286779 | G | A | 1 | a0001c0001t0002g0080 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-48+5069C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286779 | |||||||
| chr5:180286822 | C | T | 92 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0125 others(89): Show |
95 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-48+5026G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286822 | |||||||
| chr5:180286877 | T | A | 1 | a0001c0001t0004g0333 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48+4971A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286877 | |||||||
| chr5:180287085 | T | C | 1 | a0001c0001t0003g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-48+4763A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287085 | |||||||
| chr5:180287155 | A | G | 159 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0207 others(156): Show |
168 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.-48+4693T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287155 | |||||||
| chr5:180287235 | C | G | 1 | a0001c0001t0040g0208 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-48+4613G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287235 | |||||||
| chr5:180287388 | G | A | 1 | a0001c0001t0008g0081 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-48+4460C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287388 | |||||||
| chr5:180287413 | T | C | 1 | a0001c0001t0005g0306 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-48+4435A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287413 | |||||||
| chr5:180287453 | T | C | 2 | a0001c0001t0026g0291 a0001c0001t0026g0293 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-48+4395A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287453 | |||||||
| chr5:180287659 | T | C | 1 | a0001c0001t0005g0304 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-48+4189A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287659 | |||||||
| chr5:180287699 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-48+4149T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287699 | |||||||
| chr5:180287733 | T | C | 40 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0050 others(37): Show |
48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-48+4115A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287733 | |||||||
| chr5:180287803 | G | A | 1 | a0001c0001t0044g0340 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-48+4045C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287803 | |||||||
| chr5:180287876 | A | C | 3 | a0001c0001t0022g0341 a0001c0001t0022g0342 a0001c0001t0022g0343 |
3 | HG01884.hp2 HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-48+3972T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287876 | |||||||
| chr5:180287981 | G | A | 40 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0050 others(37): Show |
48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-48+3867C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287981 | |||||||
| chr5:180288059 | C | T | 40 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0050 others(37): Show |
48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-48+3789G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288059 | |||||||
| chr5:180288061 | C | T | 1 | a0001c0001t0008g0053 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-48+3787G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288061 | |||||||
| chr5:180288082 | G | T | 3 | a0001c0001t0005g0292 a0001c0001t0026g0291 a0001c0001t0026g0293 |
3 | HG02647.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-48+3766C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288082 | |||||||
| chr5:180288086 | C | A | 10 | a0001c0001t0001g0205 a0001c0001t0008g0046 a0001c0001t0020g0204 others(7): Show |
10 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-48+3762G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288086 | |||||||
| chr5:180288162 | C | T | 1 | a0001c0001t0006g0035 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-48+3686G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288162 | |||||||
| chr5:180288270 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-48+3578G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288270 | |||||||
| chr5:180288317 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3531C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288317 | |||||||
| chr5:180288318 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3530C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288318 | |||||||
| chr5:180288319 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3529C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288319 | |||||||
| chr5:180288323 | T | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3525A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288323 | |||||||
| chr5:180288325 | T | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3523A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288325 | |||||||
| chr5:180288326 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3522C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288326 | |||||||
| chr5:180288327 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3521C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288327 | |||||||
| chr5:180288330 | T | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3518A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288330 | |||||||
| chr5:180288332 | A | T | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3516T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288332 | |||||||
| chr5:180288335 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3513C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288335 | |||||||
| chr5:180288340 | T | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3508A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288340 | |||||||
| chr5:180288346 | G | T | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3502C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288346 | |||||||
| chr5:180288349 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3499C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288349 | |||||||
| chr5:180288355 | T | C | 40 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0050 others(37): Show |
48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-48+3493A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288355 | |||||||
| chr5:180288356 | C | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3492G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288356 | |||||||
| chr5:180288357 | C | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3491G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288357 | |||||||
| chr5:180288358 | A | G | 40 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0050 others(37): Show |
48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-48+3490T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288358 | |||||||
| chr5:180288359 | A | T | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3489T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288359 | |||||||
| chr5:180288360 | T | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3488A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288360 | |||||||
| chr5:180288362 | A | T | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3486T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288362 | |||||||
| chr5:180288366 | A | T | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3482T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288366 | |||||||
| chr5:180288368 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3480C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288368 | |||||||
| chr5:180288369 | T | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3479A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288369 | |||||||
| chr5:180288372 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3476C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288372 | |||||||
| chr5:180288373 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3475C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288373 | |||||||
| chr5:180288374 | C | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3474G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288374 | |||||||
| chr5:180288376 | T | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3472A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288376 | |||||||
| chr5:180288377 | T | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3471A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288377 | |||||||
| chr5:180288380 | C | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3468G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288380 | |||||||
| chr5:180288385 | T | C | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3463A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288385 | |||||||
| chr5:180288404 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3444C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288404 | |||||||
| chr5:180288405 | G | T | 1 | a0001c0001t0003g0083 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3443C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288405 | |||||||
| chr5:180288426 | A | C | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-48+3422T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288426 | |||||||
| chr5:180288519 | C | CGAAGTGT others(35): Show |
1 | a0001c0001t0001g0254 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-48+3287_-48+3328d others(44): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288519 | |||||||
| chr5:180288598 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-48+3250C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288598 | |||||||
| chr5:180288622 | C | G | 1 | a0001c0001t0045g0344 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-48+3226G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288622 | |||||||
| chr5:180288803 | A | G | 110 | a0001c0001t0001g0019 a0001c0001t0001g0236 a0001c0001t0001g0237 others(107): Show |
123 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-48+3045T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288803 | |||||||
| chr5:180288828 | A | C | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-48+3020T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288828 | |||||||
| chr5:180288836 | C | A | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-48+3012G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288836 | |||||||
| chr5:180288869 | A | C | 143 | a0001c0001t0001g0020 a0001c0001t0001g0205 a0001c0001t0001g0207 others(140): Show |
155 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(152): Show |
intron_variant | MODIFIER | c.-48+2979T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288869 | |||||||
| chr5:180288982 | CA | C | 4 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(1): Show |
4 | NA18954.hp2 NA18955.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+2865delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288982 | |||||||
| chr5:180289070 | T | C | 11 | a0001c0001t0001g0205 a0001c0001t0008g0046 a0001c0001t0020g0204 others(8): Show |
11 | HG01884.hp2 HG02145.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-48+2778A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289070 | |||||||
| chr5:180289076 | C | A | 2 | a0001c0001t0002g0114 a0001c0001t0002g0115 |
2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-48+2772G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289076 | |||||||
| chr5:180289137 | G | A | 1 | a0001c0001t0021g0263 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-48+2711C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289137 | |||||||
| chr5:180289240 | C | T | 1 | a0001c0001t0012g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-48+2608G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289240 | |||||||
| chr5:180289265 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-48+2583T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289265 | |||||||
| chr5:180289336 | G | A | 169 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0205 others(166): Show |
184 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.-48+2512C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289336 | |||||||
| chr5:180289396 | C | G | 1 | a0001c0001t0026g0291 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-48+2452G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289396 | |||||||
| chr5:180289477 | T | C | 1 | a0001c0001t0001g0264 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-48+2371A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289477 | |||||||
| chr5:180289533 | G | A | 3 | a0001c0001t0005g0292 a0001c0001t0026g0291 a0001c0001t0026g0293 |
3 | HG02647.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-48+2315C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289533 | |||||||
| chr5:180289751 | G | A | 40 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0050 others(37): Show |
48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-48+2097C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289751 | |||||||
| chr5:180289932 | T | C | 2 | a0001c0001t0002g0114 a0001c0001t0002g0115 |
2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-48+1916A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289932 | |||||||
| chr5:180290046 | C | CAG | 332 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(329): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.-48+1800_-48+1801d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290046 | |||||||
| chr5:180290446 | C | T | 66 | a0001c0001t0001g0019 a0001c0001t0001g0126 a0001c0001t0001g0236 others(63): Show |
73 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-48+1402G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290446 | |||||||
| chr5:180290460 | T | C | 2 | a0001c0001t0005g0336 a0001c0001t0005g0337 |
2 | NA18972.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-48+1388A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290460 | |||||||
| chr5:180290498 | T | C | 7 | a0001c0001t0022g0341 a0001c0001t0022g0342 a0001c0001t0022g0343 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48+1350A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290498 | |||||||
| chr5:180290643 | T | A | 123 | a0001c0001t0001g0020 a0001c0001t0001g0236 a0001c0001t0001g0237 others(120): Show |
135 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.-48+1205A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290643 | |||||||
| chr5:180290720 | C | T | 1 | a0001c0001t0036g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-48+1128G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290720 | |||||||
| chr5:180290849 | G | A | 1 | a0001c0001t0013g0247 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-48+999C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290849 | |||||||
| chr5:180290943 | T | A | 2 | a0001c0001t0003g0119 a0001c0001t0016g0120 |
2 | HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-48+905A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290943 | |||||||
| chr5:180290979 | TTTAAATA others(3): Show |
T | 1 | a0001c0001t0038g0136 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-48+859_-48+868del others(10): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290979 | |||||||
| chr5:180291131 | C | T | 13 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(10): Show |
14 | HG00099.hp2 HG01258.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.-48+717G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291131 | |||||||
| chr5:180291134 | AGG | A | 16 | a0001c0001t0001g0020 a0001c0001t0001g0269 a0001c0001t0001g0270 others(13): Show |
17 | HG00609.hp2 HG00642.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+712_-48+713del others(2): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291134 | |||||||
| chr5:180291189 | G | C | 68 | a0001c0001t0001g0019 a0001c0001t0001g0248 a0001c0001t0001g0249 others(65): Show |
72 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.-48+659C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291189 | |||||||
| chr5:180291330 | G | C | 3 | a0001c0001t0023g0121 a0001c0001t0023g0122 a0001c0001t0025g0284 |
3 | HG02965.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-48+518C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291330 | |||||||
| chr5:180291478 | G | A | 1 | a0001c0001t0009g0266 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-48+370C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291478 | |||||||
| chr5:180291486 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-48+362G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291486 | |||||||
| chr5:180291501 | G | A | 1 | a0001c0001t0007g0267 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-48+347C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291501 | |||||||
| chr5:180291699 | C | T | 1 | a0001c0001t0044g0340 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-48+149G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291699 | |||||||
| chr5:180291762 | C | T | 1 | a0001c0001t0005g0285 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-48+86G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291762 | |||||||
| chr5:180291763 | C | G | 2 | a0001c0001t0018g0123 a0001c0001t0018g0124 |
2 | HG01099.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.-48+85G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291763 | |||||||
| chr5:180291765 | G | C | 1 | a0001c0001t0001g0268 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-48+83C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291765 | |||||||
| chr5:180291804 | G | A | 24 | a0001c0001t0001g0020 a0001c0001t0001g0269 a0001c0001t0001g0270 others(21): Show |
25 | HG00609.hp2 HG00642.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.-48+44C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291804 |