Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6885 |
| ensemblid | ENSG00000135341.19 |
| hgncid | 6859 |
| symbol | MAP3K7 |
| name | mitogen-activated protein kinase kinase kinase 7 |
| refseq_nuc | NM_145331.3 |
| refseq_prot | NP_663304.1 |
| ensembl_nuc | ENST00000369329.8 |
| ensembl_prot | ENSP00000358335.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 90513579 |
| end | 90587072 |
| strand | - |
| ver | v1.2 |
| region | chr6:90513579-90587072 |
| region5000 | chr6:90508579-90592072 |
| regionname0 | MAP3K7_chr6_90513579_90587072 |
| regionname5000 | MAP3K7_chr6_90508579_90592072 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 606 | 343 | 84 | 66 | 139 | 12 | 40 | 105 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | MSTAS others(601): Show |
chr6 | 90508579 | 90592072 |
| a0002 | 0/0 | 442 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | MSTAS others(437): Show |
chr6 | 90508579 | 90592072 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1818 | 341 | 82 | 66 | 139 | 12 | 40 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | ATGTC others(1813): Show |
chr6 | 90508579 | 90592072 | ||
| a0001c0002 | 0/0 | 1818 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | ATGTC others(1813): Show |
chr6 | 90508579 | 90592072 | ||
| a0002c0003 | 0/0 | 1818 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | ATGTC others(1813): Show |
chr6 | 90508579 | 90592072 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4932 | 115 | 12 | 27 | 62 | 0 | 13 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4927): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0002 | 0/1 | 4924 | 71 | 4 | 12 | 38 | 4 | 12 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0003 | 0/0 | 4924 | 42 | 7 | 10 | 16 | 4 | 5 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0004 | 0/0 | 4924 | 31 | 27 | 4 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0005 | 0/0 | 4924 | 18 | 4 | 6 | 3 | 2 | 3 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0006 | 0/0 | 4923 | 17 | 1 | 2 | 9 | 1 | 4 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4918): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0007 | 0/0 | 4925 | 10 | 10 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4920): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0008 | 0/0 | 4924 | 10 | 0 | 2 | 8 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0009 | 0/0 | 4924 | 5 | 2 | 1 | 0 | 0 | 2 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0010 | 0/0 | 4932 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4927): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0011 | 0/0 | 4932 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4927): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0012 | 0/0 | 4924 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0013 | 0/0 | 4924 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0014 | 0/0 | 4924 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0015 | 0/0 | 4924 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | CGCGA others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0016 | 0/0 | 4924 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0017 | 0/0 | 4924 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0018 | 0/0 | 4924 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0019 | 0/0 | 4932 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4927): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0020 | 0/0 | 4924 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0021 | 0/0 | 4932 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4927): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0022 | 0/0 | 4932 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4927): Show |
chr6 | 90508579 | 90592072 |
| a0001c0001t0023 | 0/0 | 4924 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0001c0002t0004 | 0/0 | 4924 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4919): Show |
chr6 | 90508579 | 90592072 |
| a0002c0003t0006 | 0/0 | 4923 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | GGCGG others(4918): Show |
chr6 | 90508579 | 90592072 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0260 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0004 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0005g0002 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0005g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0006g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0007g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0007g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0008g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0008g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0008g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0008g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0008g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0009g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0009g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0009g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0009g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0010g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0010g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0010g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0011g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0011g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0012g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0013g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0013g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0014g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0014g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0015g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0016g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0017g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0018g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0019g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0020g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0021g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0022g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0001t0023g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0002t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0001c0002t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| a0002c0003t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0103 | EUR | GBR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0136 | EUR | GBR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0180 | EUR | FIN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0098 | EUR | FIN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0065 | EUR | FIN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0048 | EUR | FIN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00597 | hp1 | a0001 | c0001 | t0008 | g0070 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0061 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00733 | hp2 | a0001 | c0001 | t0009 | g0126 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00735 | hp2 | a0001 | c0001 | t0020 | g0057 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0121 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0152 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0059 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0139 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0056 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01261 | hp2 | a0001 | c0001 | t0015 | g0044 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0094 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0149 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0114 | EUR | IBS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01515 | hp2 | a0001 | c0001 | t0017 | g0051 | EUR | IBS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0164 | EUR | IBS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0109 | EUR | IBS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0155 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01975 | hp2 | a0001 | c0001 | t0008 | g0112 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0147 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0148 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02129 | hp2 | a0001 | c0001 | t0012 | g0021 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02132 | hp1 | a0001 | c0001 | t0012 | g0021 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02132 | hp2 | a0001 | c0001 | t0008 | g0078 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02135 | hp1 | a0001 | c0001 | t0006 | g0145 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0161 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0162 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CDX | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | CDX | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CDX | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | CDX | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0154 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02273 | hp1 | a0001 | c0001 | t0008 | g0003 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0196 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0110 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0031 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0002 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0205 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02630 | hp2 | a0001 | c0001 | t0022 | g0047 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0045 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0033 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02698 | hp1 | a0001 | c0001 | t0009 | g0127 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02717 | hp1 | a0001 | c0001 | t0010 | g0043 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02717 | hp2 | a0001 | c0001 | t0021 | g0067 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0186 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02922 | hp1 | a0001 | c0001 | t0018 | g0254 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0093 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0031 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0066 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03130 | hp1 | a0001 | c0002 | t0004 | g0129 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03130 | hp2 | a0001 | c0001 | t0014 | g0116 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0263 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03139 | hp2 | a0001 | c0001 | t0013 | g0249 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0091 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0130 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0016 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0016 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0132 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0118 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0043 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0064 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0063 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03579 | hp2 | a0001 | c0001 | t0023 | g0068 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0140 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0012 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03942 | hp1 | a0001 | c0001 | t0009 | g0125 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0016 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0058 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0217 | AFR | YRI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | CHB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | YRI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | YRI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18944 | hp2 | a0001 | c0001 | t0006 | g0142 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0134 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18974 | hp1 | a0002 | c0003 | t0006 | g0146 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18977 | hp1 | a0001 | c0001 | t0006 | g0143 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18979 | hp2 | a0001 | c0001 | t0008 | g0101 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18982 | hp2 | a0001 | c0001 | t0006 | g0133 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18987 | hp1 | a0001 | c0001 | t0019 | g0227 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18987 | hp2 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18994 | hp2 | a0001 | c0001 | t0008 | g0157 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | LWK | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | LWK | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | LWK | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19060 | hp2 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19065 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19080 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | YRI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0115 | AFR | YRI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ASW | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0060 | AFR | ASW | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0182 | EUR | TSI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0002 | EUR | TSI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA20905 | hp1 | a0001 | c0001 | t0016 | g0046 | SAS | GIH | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | GIH | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0080 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0131 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG03471 | hp2 | a0001 | c0001 | t0013 | g0069 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | USA | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | USA | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | USA | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | USA | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | LWK | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | LWK | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0128 | REF | REF | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0260 | REF | REF | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:90536351 | T | A | 1 | a0002 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1342A>T | p.Thr448Ser | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1531/4932 | 1342/1821 | 448/606 | chr6 | 90536351 | |||
| chr6:90536362 | G | A | 1 | a0002 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1331C>T | p.Thr444Ile | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1520/4932 | 1331/1821 | 444/606 | chr6 | 90536362 | |||
| chr6:90536365 | A | C | 1 | a0002 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1328T>G | p.Leu443Trp | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1517/4932 | 1328/1821 | 443/606 | chr6 | 90536365 | |||
| chr6:90536378 | A | T | 1 | a0002 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1315T>A | p.Ser439Thr | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1504/4932 | 1315/1821 | 439/606 | chr6 | 90536378 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:90516567 | G | A | 1 | a0001c0002 | 2 | HG03130.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.1755C>T | p.Tyr585Tyr | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1944/4932 | 1755/1821 | 585/606 | chr6 | 90516567 | |||
| chr6:90536349 | T | A | 1 | a0002c0003 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.1344A>T | p.Thr448Thr | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1533/4932 | 1344/1821 | 448/606 | chr6 | 90536349 | |||
| chr6:90536352 | T | A | 1 | a0002c0003 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.1341A>T | p.Gly447Gly | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1530/4932 | 1341/1821 | 447/606 | chr6 | 90536352 | |||
| chr6:90536364 | C | T | 1 | a0002c0003 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.1329G>A | p.Leu443Leu | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1518/4932 | 1329/1821 | 443/606 | chr6 | 90536364 | |||
| chr6:90536367 | G | A | 1 | a0002c0003 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.1326C>T | p.Asp442Asp | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1515/4932 | 1326/1821 | 442/606 | chr6 | 90536367 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:90513648 | T | C | 1 | a0001c0001t0017 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2853A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 2853 | chr6 | 90513648 | ||||||
| chr6:90513723 | C | T | 2 | a0001c0001t0006 a0002c0003t0006 |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2778G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 2778 | chr6 | 90513723 | ||||||
| chr6:90513731 | G | A | 1 | a0001c0001t0013 | 2 | HG03139.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2770C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 2770 | chr6 | 90513731 | ||||||
| chr6:90513901 | C | T | 21 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(18): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*2600G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 2600 | chr6 | 90513901 | ||||||
| chr6:90514022 | G | C | 1 | a0001c0001t0022 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2479C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 2479 | chr6 | 90514022 | ||||||
| chr6:90514059 | AAATGTAA others(2): Show |
A | 19 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(16): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*2433_*2441delAATT others(5): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 2433 | chr6 | 90514059 | ||||||
| chr6:90514552 | C | CT | 21 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(18): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*1948dupA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1948 | chr6 | 90514552 | ||||||
| chr6:90514653 | C | T | 6 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(3): Show |
90 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1848G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1848 | chr6 | 90514653 | ||||||
| chr6:90514666 | C | T | 1 | a0001c0001t0010 | 4 | HG02451.hp1 HG02717.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1835G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1835 | chr6 | 90514666 | ||||||
| chr6:90514681 | G | A | 2 | a0001c0001t0006 a0002c0003t0006 |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1820C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1820 | chr6 | 90514681 | ||||||
| chr6:90514792 | A | G | 1 | a0001c0001t0020 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1709T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1709 | chr6 | 90514792 | ||||||
| chr6:90514860 | AT | A | 21 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(18): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*1640delA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1640 | chr6 | 90514860 | ||||||
| chr6:90515080 | A | C | 1 | a0001c0001t0021 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1421T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1421 | chr6 | 90515080 | ||||||
| chr6:90515198 | A | T | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(14): Show |
200 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*1303T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1303 | chr6 | 90515198 | ||||||
| chr6:90515326 | A | G | 1 | a0001c0001t0019 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1175T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1175 | chr6 | 90515326 | ||||||
| chr6:90515400 | T | A | 1 | a0001c0001t0014 | 2 | HG03130.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1101A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1101 | chr6 | 90515400 | ||||||
| chr6:90515416 | C | T | 9 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(6): Show |
125 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*1085G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1085 | chr6 | 90515416 | ||||||
| chr6:90515501 | G | A | 21 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(18): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*1000C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1000 | chr6 | 90515501 | ||||||
| chr6:90515536 | T | C | 1 | a0001c0001t0018 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*965A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 965 | chr6 | 90515536 | ||||||
| chr6:90515555 | A | G | 1 | a0001c0001t0021 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*946T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 946 | chr6 | 90515555 | ||||||
| chr6:90515563 | C | CT | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(14): Show |
200 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*937dupA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 937 | chr6 | 90515563 | ||||||
| chr6:90515621 | A | AT | 1 | a0001c0001t0007 | 10 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*879dupA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 879 | chr6 | 90515621 | ||||||
| chr6:90515642 | T | C | 2 | a0001c0001t0005 a0001c0001t0020 |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*859A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 859 | chr6 | 90515642 | ||||||
| chr6:90515999 | G | A | 2 | a0001c0001t0021 a0001c0001t0022 |
2 | HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*502C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 502 | chr6 | 90515999 | ||||||
| chr6:90516018 | C | T | 2 | a0001c0001t0006 a0002c0003t0006 |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*483G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 483 | chr6 | 90516018 | ||||||
| chr6:90516157 | G | A | 1 | a0001c0001t0023 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*344C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 344 | chr6 | 90516157 | ||||||
| chr6:90516323 | T | C | 2 | a0001c0001t0006 a0002c0003t0006 |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*178A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 178 | chr6 | 90516323 | ||||||
| chr6:90516324 | T | A | 1 | a0001c0001t0009 | 5 | HG00733.hp2 HG02451.hp2 HG02698.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*177A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 177 | chr6 | 90516324 | ||||||
| chr6:90516489 | G | A | 1 | a0001c0001t0008 | 10 | HG00597.hp1 HG01975.hp2 HG02132.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*12C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 12 | chr6 | 90516489 | ||||||
| chr6:90586966 | C | G | 1 | a0001c0001t0016 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-83G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 83 | chr6 | 90586966 | ||||||
| chr6:90586990 | G | T | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-107C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | chr6 | 90586990 | |||||||
| chr6:90586991 | T | C | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-108A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 108 | chr6 | 90586991 | ||||||
| chr6:90586993 | C | G | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-110G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 110 | chr6 | 90586993 | ||||||
| chr6:90586995 | A | G | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-112T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 112 | chr6 | 90586995 | ||||||
| chr6:90586999 | C | G | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-116G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 116 | chr6 | 90586999 | ||||||
| chr6:90587015 | G | T | 1 | a0001c0001t0012 | 2 | HG02129.hp2 HG02132.hp1 |
5_prime_UTR_variant | MODIFIER | c.-132C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 132 | chr6 | 90587015 | ||||||
| chr6:90587023 | A | T | 1 | a0001c0001t0011 | 3 | HG01891.hp2 HG02258.hp2 HG02647.hp2 |
5_prime_UTR_variant | MODIFIER | c.-140T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 140 | chr6 | 90587023 | ||||||
| chr6:90587028 | G | T | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-145C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | chr6 | 90587028 | |||||||
| chr6:90587034 | A | T | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-151T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 151 | chr6 | 90587034 | ||||||
| chr6:90587042 | G | T | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-159C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 159 | chr6 | 90587042 | ||||||
| chr6:90587044 | C | T | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-161G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 161 | chr6 | 90587044 | ||||||
| chr6:90587046 | G | C | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-163C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 163 | chr6 | 90587046 | ||||||
| chr6:90587050 | C | G | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-167G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 167 | chr6 | 90587050 | ||||||
| chr6:90587051 | T | A | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-168A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | chr6 | 90587051 | |||||||
| chr6:90587052 | G | C | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-169C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 169 | chr6 | 90587052 | ||||||
| chr6:90587054 | C | G | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-171G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 171 | chr6 | 90587054 | ||||||
| chr6:90587055 | T | C | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-172A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 172 | chr6 | 90587055 | ||||||
| chr6:90587057 | C | G | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-174G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 174 | chr6 | 90587057 | ||||||
| chr6:90587058 | G | C | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-175C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 175 | chr6 | 90587058 | ||||||
| chr6:90587060 | T | A | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-177A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | chr6 | 90587060 | |||||||
| chr6:90587068 | C | T | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-185G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 185 | chr6 | 90587068 | ||||||
| chr6:90587072 | C | G | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-189G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 189 | chr6 | 90587072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:90517025 | C | T | 48 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(45): Show |
55 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1641-344G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517025 | |||||||
| chr6:90517108 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1641-427C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517108 | |||||||
| chr6:90517194 | T | C | 9 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0252 others(6): Show |
10 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1641-513A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517194 | |||||||
| chr6:90517229 | T | C | 1 | a0001c0001t0006g0149 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1641-548A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517229 | |||||||
| chr6:90517318 | G | T | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1641-637C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517318 | |||||||
| chr6:90517399 | ATAAC | A | 16 | a0001c0001t0001g0261 a0001c0001t0003g0033 a0001c0001t0003g0168 others(13): Show |
23 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1641-722_1641-719d others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517399 | |||||||
| chr6:90517628 | T | C | 1 | a0001c0002t0004g0129 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1640+819A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517628 | |||||||
| chr6:90517633 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0198 a0001c0001t0001g0233 others(2): Show |
8 | HG02129.hp1 NA18612.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.1640+814T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517633 | |||||||
| chr6:90517642 | T | C | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02109.hp2 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1640+805A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517642 | |||||||
| chr6:90517742 | C | A | 1 | a0001c0001t0007g0130 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1640+705G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517742 | |||||||
| chr6:90517877 | A | C | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02109.hp2 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1640+570T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517877 | |||||||
| chr6:90517909 | G | A | 171 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(168): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1640+538C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517909 | |||||||
| chr6:90517962 | C | T | 171 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(168): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1640+485G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517962 | |||||||
| chr6:90518087 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1640+360G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90518087 | |||||||
| chr6:90518194 | A | G | 2 | a0001c0001t0021g0067 a0001c0001t0022g0047 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1640+253T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90518194 | |||||||
| chr6:90518293 | T | C | 2 | a0001c0001t0004g0205 a0001c0001t0004g0217 |
2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1640+154A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90518293 | |||||||
| chr6:90518385 | T | A | 1 | a0001c0001t0001g0230 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1640+62A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90518385 | |||||||
| chr6:90518422 | T | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0232 a0001c0001t0001g0236 others(2): Show |
6 | HG02083.hp2 NA18942.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.1640+25A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90518422 | |||||||
| chr6:90518633 | A | G | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1525-71T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 15/16 | chr6 | 90518633 | |||||||
| chr6:90518704 | A | G | 48 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(45): Show |
55 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1525-142T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 15/16 | chr6 | 90518704 | |||||||
| chr6:90518705 | G | A | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1525-143C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 15/16 | chr6 | 90518705 | |||||||
| chr6:90518743 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1525-181A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 15/16 | chr6 | 90518743 | |||||||
| chr6:90519003 | A | C | 4 | a0001c0001t0003g0048 a0001c0001t0003g0050 a0001c0001t0003g0052 others(1): Show |
4 | HG00323.hp2 HG01358.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+255T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 15/16 | chr6 | 90519003 | |||||||
| chr6:90519214 | TAAG | T | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1524+41_1524+43del others(3): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 15/16 | chr6 | 90519214 | |||||||
| chr6:90519453 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0242 |
2 | NA18955.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1463-134A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90519453 | |||||||
| chr6:90519726 | C | T | 169 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(166): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1463-407G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90519726 | |||||||
| chr6:90519737 | A | G | 91 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(88): Show |
125 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1463-418T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90519737 | |||||||
| chr6:90519751 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1463-432C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90519751 | |||||||
| chr6:90519891 | A | G | 1 | a0001c0001t0003g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1463-572T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90519891 | |||||||
| chr6:90519952 | C | T | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1463-633G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90519952 | |||||||
| chr6:90519958 | C | G | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1463-639G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90519958 | |||||||
| chr6:90520292 | G | A | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02109.hp2 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1463-973C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90520292 | |||||||
| chr6:90520374 | GT | G | 39 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(36): Show |
45 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1463-1056delA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90520374 | |||||||
| chr6:90520565 | G | A | 1 | a0001c0001t0003g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1463-1246C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90520565 | |||||||
| chr6:90520593 | T | C | 1 | a0001c0001t0003g0151 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1463-1274A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90520593 | |||||||
| chr6:90520674 | ACTTACC | A | 18 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(15): Show |
20 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.1463-1361_1463-135 others(10): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90520674 | |||||||
| chr6:90521014 | C | T | 18 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(15): Show |
20 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.1463-1695G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521014 | |||||||
| chr6:90521048 | C | T | 171 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(168): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1463-1729G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521048 | |||||||
| chr6:90521114 | G | A | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02109.hp2 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1463-1795C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521114 | |||||||
| chr6:90521182 | A | T | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1463-1863T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521182 | |||||||
| chr6:90521257 | C | CGT | 11 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0192 others(8): Show |
16 | HG00733.hp1 HG01192.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1463-1940_1463-193 others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521257 | |||||||
| chr6:90521257 | CGT | C | 7 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0001g0207 others(4): Show |
7 | HG02109.hp2 HG02559.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1463-1940_1463-193 others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521257 | |||||||
| chr6:90521257 | CGTGT | C | 12 | a0001c0001t0003g0165 a0001c0001t0003g0169 a0001c0001t0004g0093 others(9): Show |
12 | HG00597.hp1 HG00639.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1463-1942_1463-193 others(8): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521257 | |||||||
| chr6:90521257 | CGTGTGT | C | 155 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(152): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1463-1944_1463-193 others(10): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521257 | |||||||
| chr6:90521257 | CGTGTGTG others(1): Show |
C | 2 | a0001c0001t0004g0028 a0001c0001t0004g0119 |
3 | HG02723.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1463-1946_1463-193 others(12): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521257 | |||||||
| chr6:90521257 | CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1463-1952_1463-193 others(18): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521257 | |||||||
| chr6:90521264 | G | A | 1 | a0001c0001t0003g0035 | 2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1463-1945C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521264 | |||||||
| chr6:90521497 | C | T | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1463-2178G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521497 | |||||||
| chr6:90521568 | A | G | 91 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(88): Show |
125 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1462+2110T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521568 | |||||||
| chr6:90521599 | C | T | 169 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(166): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1462+2079G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521599 | |||||||
| chr6:90521633 | C | A | 64 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(61): Show |
90 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1462+2045G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521633 | |||||||
| chr6:90521762 | CTAGATCC others(10): Show |
C | 1 | a0001c0001t0001g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1462+1899_1462+191 others(21): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521762 | |||||||
| chr6:90521791 | G | A | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1462+1887C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521791 | |||||||
| chr6:90521808 | T | G | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1462+1870A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521808 | |||||||
| chr6:90521826 | C | T | 1 | a0001c0001t0002g0013 | 3 | HG00558.hp1 NA18972.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1462+1852G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521826 | |||||||
| chr6:90521958 | G | C | 1 | a0001c0001t0002g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1462+1720C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521958 | |||||||
| chr6:90522052 | C | A | 171 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(168): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1462+1626G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522052 | |||||||
| chr6:90522260 | G | A | 171 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(168): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1462+1418C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522260 | |||||||
| chr6:90522407 | C | G | 61 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(58): Show |
74 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1462+1271G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522407 | |||||||
| chr6:90522407 | C | T | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1462+1271G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522407 | |||||||
| chr6:90522441 | C | T | 1 | a0001c0001t0006g0139 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1462+1237G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522441 | |||||||
| chr6:90522529 | T | A | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1462+1149A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522529 | |||||||
| chr6:90522894 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1462+784A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522894 | |||||||
| chr6:90522956 | T | A | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1462+722A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522956 | |||||||
| chr6:90523053 | C | T | 3 | a0001c0001t0002g0073 a0001c0001t0002g0083 a0001c0001t0023g0068 |
3 | HG01891.hp1 HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1462+625G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90523053 | |||||||
| chr6:90523264 | G | A | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1462+414C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90523264 | |||||||
| chr6:90523410 | C | T | 173 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(170): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1462+268G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90523410 | |||||||
| chr6:90523495 | G | A | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1462+183C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90523495 | |||||||
| chr6:90523840 | C | T | 20 | a0001c0001t0004g0004 a0001c0001t0004g0027 a0001c0001t0004g0028 others(17): Show |
28 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1357-57G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90523840 | |||||||
| chr6:90524020 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1357-237G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90524020 | |||||||
| chr6:90524260 | A | C | 2 | a0001c0001t0003g0175 a0001c0001t0003g0178 |
2 | NA18955.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1357-477T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90524260 | |||||||
| chr6:90524487 | A | C | 155 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(152): Show |
202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1357-704T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90524487 | |||||||
| chr6:90524640 | A | G | 48 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(45): Show |
55 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1357-857T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90524640 | |||||||
| chr6:90524707 | T | C | 173 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(170): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1357-924A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90524707 | |||||||
| chr6:90524798 | G | A | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-1015C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90524798 | |||||||
| chr6:90524860 | G | A | 31 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(28): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1357-1077C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90524860 | |||||||
| chr6:90525045 | TAA | T | 43 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(40): Show |
51 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1357-1264_1357-126 others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525045 | |||||||
| chr6:90525071 | C | T | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1357-1288G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525071 | |||||||
| chr6:90525084 | T | C | 2 | a0001c0001t0004g0029 a0001c0001t0004g0123 |
3 | HG01109.hp1 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1357-1301A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525084 | |||||||
| chr6:90525098 | G | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(21): Show |
33 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1357-1315C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525098 | |||||||
| chr6:90525109 | T | TA | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-1327dupT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525109 | |||||||
| chr6:90525516 | T | C | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1357-1733A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525516 | |||||||
| chr6:90525650 | C | G | 1 | a0001c0001t0005g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1357-1867G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525650 | |||||||
| chr6:90525770 | G | A | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-1987C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525770 | |||||||
| chr6:90525902 | C | G | 178 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0001g0207 others(175): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1357-2119G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525902 | |||||||
| chr6:90525925 | G | T | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-2142C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525925 | |||||||
| chr6:90526009 | T | C | 48 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(45): Show |
55 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1357-2226A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90526009 | |||||||
| chr6:90526245 | G | A | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-2462C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90526245 | |||||||
| chr6:90526527 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0001g0256 |
2 | HG00438.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1357-2744C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90526527 | |||||||
| chr6:90526675 | T | C | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1357-2892A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90526675 | |||||||
| chr6:90526700 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0190 |
3 | HG00558.hp2 HG02165.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1357-2917C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90526700 | |||||||
| chr6:90526820 | G | C | 2 | a0001c0001t0003g0176 a0001c0001t0003g0177 |
2 | HG03492.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1357-3037C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90526820 | |||||||
| chr6:90526870 | T | C | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-3087A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90526870 | |||||||
| chr6:90527425 | G | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1357-3642C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527425 | |||||||
| chr6:90527433 | T | A | 1 | a0001c0001t0007g0130 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1357-3650A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527433 | |||||||
| chr6:90527451 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1357-3668T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527451 | |||||||
| chr6:90527624 | T | C | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-3841A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527624 | |||||||
| chr6:90527784 | T | C | 39 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(36): Show |
45 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1357-4001A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527784 | |||||||
| chr6:90527791 | T | A | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1357-4008A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527791 | |||||||
| chr6:90527832 | A | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0095 |
2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1357-4049T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527832 | |||||||
| chr6:90527856 | TTCATAAG others(314): Show |
T | 173 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(170): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1357-4394_1357-407 others(4): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527856 | |||||||
| chr6:90527866 | C | CT | 20 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(17): Show |
23 | HG00438.hp2 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1357-4084dupA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527866 | |||||||
| chr6:90527866 | CT | C | 12 | a0001c0001t0001g0011 a0001c0001t0001g0204 a0001c0001t0001g0207 others(9): Show |
12 | HG01168.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1357-4084delA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527866 | |||||||
| chr6:90527866 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1357-4093_1357-408 others(14): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527866 | |||||||
| chr6:90527866 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0253 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1357-4095_1357-408 others(16): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527866 | |||||||
| chr6:90528180 | A | G | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-4397T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528180 | |||||||
| chr6:90528587 | C | T | 48 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(45): Show |
55 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1357-4804G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528587 | |||||||
| chr6:90528592 | C | G | 1 | a0001c0001t0001g0228 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1357-4809G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528592 | |||||||
| chr6:90528635 | ATAG | A | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-4855_1357-485 others(7): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528635 | |||||||
| chr6:90528655 | G | A | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-4872C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528655 | |||||||
| chr6:90528838 | G | A | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-5055C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528838 | |||||||
| chr6:90528848 | G | C | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1357-5065C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528848 | |||||||
| chr6:90528866 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1357-5083G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528866 | |||||||
| chr6:90529207 | T | C | 61 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(58): Show |
74 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1357-5424A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529207 | |||||||
| chr6:90529284 | C | T | 172 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(169): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1357-5501G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529284 | |||||||
| chr6:90529362 | CAT | C | 39 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(36): Show |
45 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1357-5581_1357-558 others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529362 | |||||||
| chr6:90529404 | C | T | 154 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(151): Show |
201 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1357-5621G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529404 | |||||||
| chr6:90529466 | T | C | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1357-5683A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529466 | |||||||
| chr6:90529512 | G | C | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-5729C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529512 | |||||||
| chr6:90529734 | T | C | 5 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0123 others(2): Show |
7 | HG01109.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1357-5951A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529734 | |||||||
| chr6:90529781 | T | C | 154 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(151): Show |
201 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1357-5998A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529781 | |||||||
| chr6:90529983 | T | A | 2 | a0001c0001t0002g0032 a0001c0001t0002g0077 |
3 | HG02735.hp2 HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1357-6200A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529983 | |||||||
| chr6:90529989 | A | G | 6 | a0001c0001t0006g0133 a0001c0001t0006g0134 a0001c0001t0006g0135 others(3): Show |
6 | HG02056.hp1 NA18944.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1357-6206T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529989 | |||||||
| chr6:90530187 | G | A | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1356+6150C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530187 | |||||||
| chr6:90530376 | A | G | 2 | a0001c0001t0002g0079 a0001c0001t0002g0156 |
2 | HG01081.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1356+5961T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530376 | |||||||
| chr6:90530451 | T | C | 93 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(90): Show |
127 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1356+5886A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530451 | |||||||
| chr6:90530454 | C | G | 93 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(90): Show |
127 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1356+5883G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530454 | |||||||
| chr6:90530469 | T | G | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1356+5868A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530469 | |||||||
| chr6:90530638 | A | G | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1356+5699T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530638 | |||||||
| chr6:90530689 | T | C | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1356+5648A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530689 | |||||||
| chr6:90530717 | A | G | 9 | a0001c0001t0007g0031 a0001c0001t0007g0080 a0001c0001t0007g0130 others(6): Show |
10 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1356+5620T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530717 | |||||||
| chr6:90530838 | C | T | 93 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(90): Show |
127 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1356+5499G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530838 | |||||||
| chr6:90531426 | T | A | 9 | a0001c0001t0004g0004 a0001c0001t0004g0027 a0001c0001t0004g0028 others(6): Show |
15 | HG00735.hp1 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1356+4911A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531426 | |||||||
| chr6:90531540 | A | T | 1 | a0001c0001t0001g0229 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1356+4797T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531540 | |||||||
| chr6:90531592 | G | A | 1 | a0001c0001t0006g0149 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1356+4745C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531592 | |||||||
| chr6:90531654 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1356+4683C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531654 | |||||||
| chr6:90531690 | C | T | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1356+4647G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531690 | |||||||
| chr6:90531709 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1356+4628A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531709 | |||||||
| chr6:90531770 | G | T | 172 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(169): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1356+4567C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531770 | |||||||
| chr6:90531798 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1356+4539T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531798 | |||||||
| chr6:90531904 | G | A | 7 | a0001c0001t0007g0080 a0001c0001t0007g0130 a0001c0001t0007g0131 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1356+4433C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531904 | |||||||
| chr6:90531940 | C | G | 171 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(168): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1356+4397G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531940 | |||||||
| chr6:90531956 | G | GA | 22 | a0001c0001t0001g0203 a0001c0001t0001g0220 a0001c0001t0002g0087 others(19): Show |
24 | HG00099.hp2 HG00733.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.1356+4380dupT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531956 | |||||||
| chr6:90532202 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1356+4135A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532202 | |||||||
| chr6:90532215 | T | C | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1356+4122A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532215 | |||||||
| chr6:90532319 | A | G | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1356+4018T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532319 | |||||||
| chr6:90532434 | T | C | 12 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0056 others(9): Show |
18 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1356+3903A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532434 | |||||||
| chr6:90532590 | G | A | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1356+3747C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532590 | |||||||
| chr6:90532700 | AG | A | 3 | a0001c0001t0001g0228 a0001c0001t0001g0259 a0001c0001t0001g0264 |
3 | HG01074.hp2 HG01243.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1356+3636delC | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532700 | |||||||
| chr6:90532779 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1356+3558C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532779 | |||||||
| chr6:90532818 | T | A | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1356+3519A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532818 | |||||||
| chr6:90532830 | A | G | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1356+3507T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532830 | |||||||
| chr6:90532957 | G | C | 1 | a0001c0001t0002g0006 | 4 | NA18983.hp1 NA19072.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1356+3380C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532957 | |||||||
| chr6:90533351 | G | T | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1356+2986C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90533351 | |||||||
| chr6:90533373 | G | C | 7 | a0001c0001t0004g0066 a0001c0001t0004g0093 a0001c0001t0004g0094 others(4): Show |
7 | HG01496.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1356+2964C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90533373 | |||||||
| chr6:90533416 | A | T | 172 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(169): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1356+2921T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90533416 | |||||||
| chr6:90533479 | G | A | 1 | a0001c0001t0005g0056 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1356+2858C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90533479 | |||||||
| chr6:90533482 | C | G | 1 | a0001c0001t0004g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1356+2855G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90533482 | |||||||
| chr6:90533707 | T | A | 1 | a0001c0001t0004g0117 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1356+2630A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90533707 | |||||||
| chr6:90533847 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1356+2490T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90533847 | |||||||
| chr6:90534025 | A | G | 1 | a0001c0001t0005g0065 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1356+2312T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534025 | |||||||
| chr6:90534112 | A | C | 1 | a0001c0001t0001g0226 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1356+2225T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534112 | |||||||
| chr6:90534205 | C | A | 48 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(45): Show |
55 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1356+2132G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534205 | |||||||
| chr6:90534371 | C | T | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1356+1966G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534371 | |||||||
| chr6:90534777 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1356+1560A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534777 | |||||||
| chr6:90534797 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1356+1540A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534797 | |||||||
| chr6:90534846 | T | C | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1356+1491A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534846 | |||||||
| chr6:90534914 | A | C | 2 | a0001c0002t0004g0115 a0001c0002t0004g0129 |
2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1356+1423T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534914 | |||||||
| chr6:90535010 | C | A | 6 | a0001c0001t0002g0053 a0001c0001t0002g0085 a0001c0001t0002g0089 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1356+1327G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535010 | |||||||
| chr6:90535033 | A | G | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1356+1304T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535033 | |||||||
| chr6:90535062 | A | G | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1356+1275T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535062 | |||||||
| chr6:90535102 | GATTTT | G | 39 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(36): Show |
45 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1356+1230_1356+123 others(9): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535102 | |||||||
| chr6:90535110 | TTA | T | 3 | a0001c0001t0006g0136 a0001c0001t0006g0139 a0001c0001t0006g0162 |
3 | HG00099.hp2 HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1356+1225_1356+122 others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535110 | |||||||
| chr6:90535113 | T | C | 92 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(89): Show |
126 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1356+1224A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535113 | |||||||
| chr6:90535185 | C | G | 4 | a0001c0001t0003g0034 a0001c0001t0003g0151 a0001c0001t0003g0184 others(1): Show |
5 | HG01071.hp1 HG01074.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1356+1152G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535185 | |||||||
| chr6:90535306 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1356+1031T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535306 | |||||||
| chr6:90535474 | T | C | 7 | a0001c0001t0007g0080 a0001c0001t0007g0130 a0001c0001t0007g0131 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1356+863A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535474 | |||||||
| chr6:90535811 | C | G | 7 | a0001c0001t0004g0066 a0001c0001t0004g0093 a0001c0001t0004g0094 others(4): Show |
7 | HG01496.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1356+526G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535811 | |||||||
| chr6:90535993 | T | C | 172 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(169): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1356+344A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535993 | |||||||
| chr6:90536090 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1356+247T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90536090 | |||||||
| chr6:90536157 | T | A | 3 | a0001c0001t0006g0136 a0001c0001t0006g0139 a0001c0001t0006g0162 |
3 | HG00099.hp2 HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1356+180A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90536157 | |||||||
| chr6:90536179 | GT | G | 3 | a0001c0001t0001g0252 a0001c0001t0003g0033 a0001c0001t0003g0170 |
4 | HG00738.hp2 HG01433.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1356+157delA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90536179 | |||||||
| chr6:90536288 | T | A | 16 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(13): Show |
18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1356+49A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90536288 | |||||||
| chr6:90536405 | T | G | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | splice_region_variant&intron_variant | LOW | c.1292-4A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536405 | |||||||
| chr6:90536408 | A | T | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | splice_region_variant&intron_variant | LOW | c.1292-7T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536408 | |||||||
| chr6:90536410 | A | G | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-9T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536410 | |||||||
| chr6:90536418 | A | T | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-17T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536418 | |||||||
| chr6:90536423 | T | G | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-22A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536423 | |||||||
| chr6:90536432 | A | G | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-31T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536432 | |||||||
| chr6:90536433 | A | T | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-32T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536433 | |||||||
| chr6:90536435 | A | T | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-34T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536435 | |||||||
| chr6:90536440 | G | C | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-39C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536440 | |||||||
| chr6:90536444 | A | G | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-43T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536444 | |||||||
| chr6:90536453 | A | T | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-52T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536453 | |||||||
| chr6:90536458 | G | T | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-57C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536458 | |||||||
| chr6:90536460 | G | T | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-59C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536460 | |||||||
| chr6:90536463 | A | G | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-62T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536463 | |||||||
| chr6:90536486 | T | G | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-85A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536486 | |||||||
| chr6:90536487 | T | A | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-86A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536487 | |||||||
| chr6:90536488 | T | A | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-87A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536488 | |||||||
| chr6:90536489 | G | T | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-88C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536489 | |||||||
| chr6:90536502 | T | C | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-101A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536502 | |||||||
| chr6:90536514 | G | A | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-113C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536514 | |||||||
| chr6:90536515 | T | C | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-114A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536515 | |||||||
| chr6:90536518 | G | A | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-117C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536518 | |||||||
| chr6:90536519 | T | G | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-118A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536519 | |||||||
| chr6:90536524 | A | G | 1 | a0002c0003t0006g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-123T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536524 | |||||||
| chr6:90536619 | G | T | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1292-218C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536619 | |||||||
| chr6:90536706 | T | C | 1 | a0001c0001t0014g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1292-305A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536706 | |||||||
| chr6:90537105 | C | T | 1 | a0001c0001t0004g0121 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1292-704G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90537105 | |||||||
| chr6:90537590 | T | G | 3 | a0001c0001t0007g0080 a0001c0001t0013g0069 a0001c0001t0013g0249 |
3 | HG02486.hp2 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1292-1189A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90537590 | |||||||
| chr6:90537609 | G | A | 1 | a0001c0001t0004g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1292-1208C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90537609 | |||||||
| chr6:90537808 | A | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0095 |
2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1292-1407T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90537808 | |||||||
| chr6:90537981 | A | G | 10 | a0001c0001t0003g0033 a0001c0001t0003g0151 a0001c0001t0003g0152 others(7): Show |
11 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-1580T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90537981 | |||||||
| chr6:90538114 | G | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0221 |
3 | NA18979.hp1 NA19001.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1292-1713C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90538114 | |||||||
| chr6:90538472 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1292-2071T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90538472 | |||||||
| chr6:90538692 | T | G | 1 | a0001c0001t0006g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1292-2291A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90538692 | |||||||
| chr6:90538737 | C | T | 1 | a0001c0001t0004g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1292-2336G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90538737 | |||||||
| chr6:90538780 | T | C | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1292-2379A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90538780 | |||||||
| chr6:90538844 | T | C | 4 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0123 others(1): Show |
6 | HG01109.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-2443A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90538844 | |||||||
| chr6:90538991 | G | A | 8 | a0001c0001t0007g0031 a0001c0001t0007g0130 a0001c0001t0007g0131 others(5): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-2590C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90538991 | |||||||
| chr6:90539024 | T | C | 13 | a0001c0001t0002g0013 a0001c0001t0002g0015 a0001c0001t0002g0032 others(10): Show |
19 | HG00558.hp1 HG01069.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.1292-2623A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539024 | |||||||
| chr6:90539053 | A | T | 2 | a0001c0001t0001g0223 a0001c0001t0001g0256 |
2 | HG00438.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1292-2652T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539053 | |||||||
| chr6:90539069 | T | C | 1 | a0001c0001t0002g0024 | 2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1292-2668A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539069 | |||||||
| chr6:90539100 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1292-2699C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539100 | |||||||
| chr6:90539101 | T | C | 14 | a0001c0001t0003g0034 a0001c0001t0005g0002 a0001c0001t0005g0012 others(11): Show |
21 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1292-2700A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539101 | |||||||
| chr6:90539164 | T | C | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1292-2763A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539164 | |||||||
| chr6:90539249 | C | G | 171 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(168): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1292-2848G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539249 | |||||||
| chr6:90539499 | G | A | 168 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(165): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1292-3098C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539499 | |||||||
| chr6:90539632 | C | T | 174 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0001g0207 others(171): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1292-3231G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539632 | |||||||
| chr6:90539633 | C | T | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1292-3232G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539633 | |||||||
| chr6:90539865 | A | G | 171 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(168): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1292-3464T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539865 | |||||||
| chr6:90539985 | C | T | 4 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0174 others(1): Show |
4 | NA18939.hp2 NA18948.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-3584G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539985 | |||||||
| chr6:90540035 | C | T | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1292-3634G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540035 | |||||||
| chr6:90540137 | G | T | 36 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(33): Show |
42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1292-3736C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540137 | |||||||
| chr6:90540192 | G | C | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1292-3791C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540192 | |||||||
| chr6:90540200 | T | C | 1 | a0001c0001t0003g0052 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1292-3799A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540200 | |||||||
| chr6:90540522 | C | T | 146 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(143): Show |
193 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1291+4030G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540522 | |||||||
| chr6:90540729 | A | G | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1291+3823T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540729 | |||||||
| chr6:90540761 | G | A | 2 | a0001c0001t0004g0004 a0001c0001t0004g0159 |
6 | HG00735.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291+3791C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540761 | |||||||
| chr6:90540965 | T | C | 1 | a0001c0001t0004g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1291+3587A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540965 | |||||||
| chr6:90541094 | T | G | 1 | a0001c0001t0001g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1291+3458A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90541094 | |||||||
| chr6:90541128 | T | A | 1 | a0001c0001t0006g0149 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1291+3424A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90541128 | |||||||
| chr6:90541476 | C | A | 4 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0004g0093 others(1): Show |
4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+3076G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90541476 | |||||||
| chr6:90541671 | T | C | 1 | a0001c0001t0005g0062 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1291+2881A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90541671 | |||||||
| chr6:90541717 | C | T | 3 | a0001c0001t0003g0007 a0001c0001t0003g0181 a0001c0001t0003g0183 |
6 | HG02165.hp2 NA18612.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291+2835G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90541717 | |||||||
| chr6:90541793 | G | T | 1 | a0001c0001t0005g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1291+2759C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90541793 | |||||||
| chr6:90542114 | AAAACAAT others(6): Show |
A | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1291+2425_1291+243 others(17): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542114 | |||||||
| chr6:90542130 | A | T | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1291+2422T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542130 | |||||||
| chr6:90542539 | A | G | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1291+2013T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542539 | |||||||
| chr6:90542570 | T | G | 6 | a0001c0001t0006g0133 a0001c0001t0006g0134 a0001c0001t0006g0135 others(3): Show |
6 | HG02056.hp1 NA18944.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291+1982A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542570 | |||||||
| chr6:90542636 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1291+1916T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542636 | |||||||
| chr6:90542708 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1291+1844C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542708 | |||||||
| chr6:90542817 | AT | A | 6 | a0001c0001t0007g0130 a0001c0001t0007g0131 a0001c0001t0007g0132 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291+1734delA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542817 | |||||||
| chr6:90542912 | G | C | 4 | a0001c0001t0003g0048 a0001c0001t0003g0050 a0001c0001t0003g0052 others(1): Show |
4 | HG00323.hp2 HG01358.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+1640C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542912 | |||||||
| chr6:90543090 | GGTAT | G | 146 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(143): Show |
193 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1291+1458_1291+146 others(8): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90543090 | |||||||
| chr6:90543127 | C | T | 1 | a0001c0001t0005g0060 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1291+1425G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90543127 | |||||||
| chr6:90543867 | A | G | 64 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(61): Show |
90 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1291+685T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90543867 | |||||||
| chr6:90544033 | A | T | 36 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(33): Show |
42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1291+519T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90544033 | |||||||
| chr6:90544162 | G | A | 1 | a0001c0001t0003g0049 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1291+390C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90544162 | |||||||
| chr6:90544437 | G | A | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1291+115C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90544437 | |||||||
| chr6:90544677 | C | G | 2 | a0001c0001t0005g0002 a0001c0001t0005g0058 |
6 | HG01099.hp1 HG01934.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1211-45G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90544677 | |||||||
| chr6:90544974 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1211-342C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90544974 | |||||||
| chr6:90544978 | A | T | 1 | a0001c0001t0001g0232 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1211-346T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90544978 | |||||||
| chr6:90545147 | TTGTAG | T | 64 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(61): Show |
90 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1211-520_1211-516d others(7): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545147 | |||||||
| chr6:90545152 | G | A | 108 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0001g0207 others(105): Show |
131 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1211-520C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545152 | |||||||
| chr6:90545172 | T | C | 4 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0004g0093 others(1): Show |
4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211-540A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545172 | |||||||
| chr6:90545243 | G | A | 87 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(84): Show |
121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1211-611C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545243 | |||||||
| chr6:90545270 | A | C | 1 | a0001c0001t0004g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1211-638T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545270 | |||||||
| chr6:90545423 | T | C | 3 | a0001c0001t0003g0153 a0001c0001t0003g0163 a0001c0001t0003g0172 |
3 | HG00609.hp1 NA19075.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1211-791A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545423 | |||||||
| chr6:90545545 | G | T | 1 | a0001c0001t0002g0099 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1211-913C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545545 | |||||||
| chr6:90545615 | G | A | 57 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(54): Show |
70 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1211-983C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545615 | |||||||
| chr6:90545651 | G | A | 86 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(83): Show |
120 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1211-1019C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545651 | |||||||
| chr6:90545703 | G | A | 2 | a0001c0001t0007g0132 a0001c0001t0007g0161 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1211-1071C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545703 | |||||||
| chr6:90545821 | G | A | 8 | a0001c0001t0007g0031 a0001c0001t0007g0130 a0001c0001t0007g0131 others(5): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1211-1189C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545821 | |||||||
| chr6:90545839 | G | T | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1211-1207C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545839 | |||||||
| chr6:90545876 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1211-1244T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545876 | |||||||
| chr6:90545946 | T | C | 1 | a0001c0001t0005g0062 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1210+1312A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545946 | |||||||
| chr6:90546121 | A | G | 3 | a0001c0001t0001g0224 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | NA18955.hp2 NA19012.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1210+1137T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90546121 | |||||||
| chr6:90546330 | G | A | 1 | a0001c0001t0006g0149 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1210+928C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90546330 | |||||||
| chr6:90546373 | A | G | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1210+885T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90546373 | |||||||
| chr6:90546374 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1210+884A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90546374 | |||||||
| chr6:90546942 | G | C | 18 | a0001c0001t0004g0004 a0001c0001t0004g0027 a0001c0001t0004g0028 others(15): Show |
26 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1210+316C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90546942 | |||||||
| chr6:90546958 | CA | C | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1210+299delT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90546958 | |||||||
| chr6:90546959 | A | C | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0252 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1210+299T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90546959 | |||||||
| chr6:90547117 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0004g0093 others(1): Show |
4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1210+141G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90547117 | |||||||
| chr6:90547152 | A | T | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1210+106T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90547152 | |||||||
| chr6:90547209 | A | T | 64 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(61): Show |
90 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1210+49T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90547209 | |||||||
| chr6:90547772 | A | G | 2 | a0001c0001t0001g0223 a0001c0001t0001g0256 |
2 | HG00438.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1080+275T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 10/16 | chr6 | 90547772 | |||||||
| chr6:90547966 | T | C | 1 | a0001c0001t0018g0254 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1080+81A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 10/16 | chr6 | 90547966 | |||||||
| chr6:90548027 | C | G | 1 | a0001c0001t0003g0182 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1080+20G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 10/16 | chr6 | 90548027 | |||||||
| chr6:90548300 | T | C | 5 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.950-123A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548300 | |||||||
| chr6:90548301 | T | A | 5 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.950-124A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548301 | |||||||
| chr6:90548321 | A | G | 1 | a0001c0001t0003g0153 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.950-144T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548321 | |||||||
| chr6:90548485 | T | C | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.950-308A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548485 | |||||||
| chr6:90548538 | T | C | 36 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(33): Show |
42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.950-361A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548538 | |||||||
| chr6:90548726 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0018g0254 |
2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.950-549C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548726 | |||||||
| chr6:90548969 | C | T | 169 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(166): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.950-792G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548969 | |||||||
| chr6:90548985 | G | C | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.950-808C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548985 | |||||||
| chr6:90548994 | A | T | 1 | a0001c0002t0004g0129 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.950-817T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548994 | |||||||
| chr6:90549035 | C | T | 1 | a0001c0001t0003g0172 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.950-858G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549035 | |||||||
| chr6:90549160 | T | A | 3 | a0001c0001t0002g0025 a0001c0001t0002g0102 a0001c0001t0002g0158 |
4 | NA18946.hp2 NA18986.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.950-983A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549160 | |||||||
| chr6:90549200 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.950-1023A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549200 | |||||||
| chr6:90549282 | G | T | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.950-1105C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549282 | |||||||
| chr6:90549287 | G | A | 3 | a0001c0001t0002g0088 a0001c0001t0002g0090 a0001c0001t0002g0108 |
3 | HG03654.hp1 HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.950-1110C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549287 | |||||||
| chr6:90549289 | G | A | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.950-1112C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549289 | |||||||
| chr6:90549378 | C | T | 3 | a0001c0001t0003g0007 a0001c0001t0003g0181 a0001c0001t0003g0183 |
6 | HG02165.hp2 NA18612.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.949+1090G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549378 | |||||||
| chr6:90549450 | C | T | 1 | a0001c0001t0004g0094 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.949+1018G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549450 | |||||||
| chr6:90549476 | C | T | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.949+992G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549476 | |||||||
| chr6:90549750 | T | A | 1 | a0001c0001t0011g0045 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.949+718A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549750 | |||||||
| chr6:90549790 | A | G | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.949+678T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549790 | |||||||
| chr6:90550110 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.949+358C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90550110 | |||||||
| chr6:90550318 | G | A | 1 | a0001c0001t0003g0177 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.949+150C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90550318 | |||||||
| chr6:90550335 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0191 |
4 | HG01069.hp2 HG01071.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.949+133A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90550335 | |||||||
| chr6:90550397 | T | C | 89 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(86): Show |
123 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.949+71A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90550397 | |||||||
| chr6:90550599 | A | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0214 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.868-50T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90550599 | |||||||
| chr6:90550622 | T | C | 8 | a0001c0001t0007g0031 a0001c0001t0007g0130 a0001c0001t0007g0131 others(5): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.868-73A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90550622 | |||||||
| chr6:90550698 | T | G | 1 | a0001c0001t0001g0256 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.868-149A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90550698 | |||||||
| chr6:90550745 | T | C | 1 | a0001c0001t0006g0145 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.868-196A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90550745 | |||||||
| chr6:90550891 | G | C | 1 | a0001c0001t0003g0184 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.868-342C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90550891 | |||||||
| chr6:90550959 | G | A | 4 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0004g0093 others(1): Show |
4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-410C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90550959 | |||||||
| chr6:90551037 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.868-488G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551037 | |||||||
| chr6:90551148 | T | C | 146 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(143): Show |
193 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.868-599A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551148 | |||||||
| chr6:90551268 | A | G | 2 | a0001c0001t0005g0056 a0001c0001t0020g0057 |
2 | HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.868-719T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551268 | |||||||
| chr6:90551455 | A | C | 28 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0014 others(25): Show |
48 | HG00408.hp2 HG00597.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.867+594T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551455 | |||||||
| chr6:90551467 | T | TCA | 8 | a0001c0001t0007g0031 a0001c0001t0007g0130 a0001c0001t0007g0131 others(5): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.867+580_867+581dup others(2): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551467 | |||||||
| chr6:90551863 | GA | G | 146 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(143): Show |
193 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.867+185delT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551863 | |||||||
| chr6:90551938 | T | C | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.867+111A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551938 | |||||||
| chr6:90551985 | C | A | 1 | a0001c0001t0001g0222 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.867+64G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551985 | |||||||
| chr6:90552240 | T | A | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.737-61A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90552240 | |||||||
| chr6:90552263 | G | T | 1 | a0001c0002t0004g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.737-84C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90552263 | |||||||
| chr6:90552352 | T | C | 1 | a0001c0001t0003g0178 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.737-173A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90552352 | |||||||
| chr6:90552400 | A | C | 1 | a0001c0001t0006g0149 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.737-221T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90552400 | |||||||
| chr6:90552668 | A | G | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.737-489T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90552668 | |||||||
| chr6:90552946 | T | G | 1 | a0001c0001t0006g0147 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.736+512A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90552946 | |||||||
| chr6:90553022 | G | A | 2 | a0001c0001t0002g0083 a0001c0001t0002g0084 |
2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.736+436C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90553022 | |||||||
| chr6:90553196 | C | T | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.736+262G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90553196 | |||||||
| chr6:90553424 | A | C | 1 | a0001c0001t0009g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.736+34T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90553424 | |||||||
| chr6:90553611 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.608-25T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90553611 | |||||||
| chr6:90553713 | AACT | A | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.608-130_608-128del others(3): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90553713 | |||||||
| chr6:90553763 | G | A | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.608-177C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90553763 | |||||||
| chr6:90553895 | T | C | 8 | a0001c0001t0007g0031 a0001c0001t0007g0130 a0001c0001t0007g0131 others(5): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.608-309A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90553895 | |||||||
| chr6:90554167 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0002g0073 |
2 | HG01891.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.608-581C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554167 | |||||||
| chr6:90554175 | G | A | 1 | a0001c0001t0003g0177 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.608-589C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554175 | |||||||
| chr6:90554361 | C | T | 1 | a0001c0001t0006g0133 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.608-775G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554361 | |||||||
| chr6:90554374 | G | A | 21 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(18): Show |
23 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.608-788C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554374 | |||||||
| chr6:90554421 | T | C | 2 | a0001c0002t0004g0115 a0001c0002t0004g0129 |
2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.608-835A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554421 | |||||||
| chr6:90554552 | T | C | 64 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(61): Show |
90 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.608-966A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554552 | |||||||
| chr6:90554793 | G | C | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.608-1207C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554793 | |||||||
| chr6:90554812 | T | A | 1 | a0001c0001t0015g0044 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.608-1226A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554812 | |||||||
| chr6:90554925 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.608-1339C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554925 | |||||||
| chr6:90555047 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.607+1453A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555047 | |||||||
| chr6:90555079 | T | C | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.607+1421A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555079 | |||||||
| chr6:90555316 | C | T | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.607+1184G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555316 | |||||||
| chr6:90555317 | A | G | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.607+1183T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555317 | |||||||
| chr6:90555350 | G | A | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.607+1150C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555350 | |||||||
| chr6:90555396 | C | T | 1 | a0001c0001t0006g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.607+1104G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555396 | |||||||
| chr6:90555417 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.607+1083C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555417 | |||||||
| chr6:90555476 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.607+1024G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555476 | |||||||
| chr6:90555734 | G | A | 1 | a0001c0001t0004g0160 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.607+766C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555734 | |||||||
| chr6:90556027 | G | A | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.607+473C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90556027 | |||||||
| chr6:90556063 | G | A | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.607+437C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90556063 | |||||||
| chr6:90556166 | G | A | 1 | a0001c0001t0007g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.607+334C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90556166 | |||||||
| chr6:90556210 | G | A | 2 | a0001c0002t0004g0115 a0001c0002t0004g0129 |
2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.607+290C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90556210 | |||||||
| chr6:90556219 | T | C | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.607+281A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90556219 | |||||||
| chr6:90556630 | T | TA | 87 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(84): Show |
121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
splice_region_variant&intron_variant | LOW | c.483-7dupT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90556630 | |||||||
| chr6:90556631 | A | T | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.483-7T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90556631 | |||||||
| chr6:90556783 | C | T | 1 | a0001c0001t0011g0045 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.483-159G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90556783 | |||||||
| chr6:90556880 | G | C | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.483-256C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90556880 | |||||||
| chr6:90557023 | A | ATAATT | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.483-400_483-399ins others(5): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90557023 | |||||||
| chr6:90557147 | G | A | 1 | a0001c0001t0006g0139 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.483-523C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90557147 | |||||||
| chr6:90557275 | C | T | 10 | a0001c0001t0006g0133 a0001c0001t0006g0134 a0001c0001t0006g0135 others(7): Show |
10 | HG02027.hp1 HG02056.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.483-651G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90557275 | |||||||
| chr6:90557469 | T | A | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.483-845A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90557469 | |||||||
| chr6:90557520 | C | T | 1 | a0001c0001t0014g0116 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.483-896G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90557520 | |||||||
| chr6:90557608 | T | C | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.483-984A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90557608 | |||||||
| chr6:90558308 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0004g0093 others(1): Show |
4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-1684G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558308 | |||||||
| chr6:90558319 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0214 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.483-1695G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558319 | |||||||
| chr6:90558326 | T | A | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.483-1702A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558326 | |||||||
| chr6:90558333 | T | A | 1 | a0001c0001t0002g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.483-1709A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558333 | |||||||
| chr6:90558510 | C | G | 21 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(18): Show |
23 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.482+1566G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558510 | |||||||
| chr6:90558630 | A | T | 86 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(83): Show |
120 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.482+1446T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558630 | |||||||
| chr6:90558818 | C | T | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.482+1258G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558818 | |||||||
| chr6:90558829 | T | A | 8 | a0001c0001t0007g0031 a0001c0001t0007g0130 a0001c0001t0007g0131 others(5): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.482+1247A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558829 | |||||||
| chr6:90559221 | C | A | 1 | a0001c0001t0008g0157 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.482+855G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559221 | |||||||
| chr6:90559326 | T | C | 8 | a0001c0001t0007g0031 a0001c0001t0007g0130 a0001c0001t0007g0131 others(5): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.482+750A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559326 | |||||||
| chr6:90559383 | TG | T | 167 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0001g0225 others(164): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.482+692delC | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559383 | |||||||
| chr6:90559455 | G | C | 1 | a0001c0001t0001g0231 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.482+621C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559455 | |||||||
| chr6:90559614 | T | A | 86 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(83): Show |
120 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.482+462A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559614 | |||||||
| chr6:90559615 | C | A | 86 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(83): Show |
120 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.482+461G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559615 | |||||||
| chr6:90559791 | C | A | 21 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(18): Show |
23 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.482+285G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559791 | |||||||
| chr6:90559836 | T | C | 1 | a0001c0001t0006g0139 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.482+240A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559836 | |||||||
| chr6:90559870 | A | G | 1 | a0001c0001t0005g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.482+206T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559870 | |||||||
| chr6:90560047 | C | A | 1 | a0001c0001t0003g0174 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.482+29G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90560047 | |||||||
| chr6:90560223 | G | C | 2 | a0001c0001t0007g0031 a0001c0001t0007g0186 |
3 | HG02572.hp1 HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.344-9C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560223 | |||||||
| chr6:90560240 | A | G | 1 | a0001c0001t0003g0164 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.344-26T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560240 | |||||||
| chr6:90560324 | A | G | 1 | a0001c0001t0002g0114 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.344-110T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560324 | |||||||
| chr6:90560334 | T | A | 1 | a0001c0001t0003g0048 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.344-120A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560334 | |||||||
| chr6:90560340 | C | T | 4 | a0001c0001t0007g0130 a0001c0001t0007g0131 a0001c0001t0007g0132 others(1): Show |
4 | HG02145.hp1 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-126G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560340 | |||||||
| chr6:90560376 | T | C | 1 | a0001c0001t0002g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.344-162A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560376 | |||||||
| chr6:90560457 | G | A | 86 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(83): Show |
120 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.344-243C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560457 | |||||||
| chr6:90560464 | C | T | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.344-250G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560464 | |||||||
| chr6:90560729 | T | G | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02109.hp2 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.344-515A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560729 | |||||||
| chr6:90561077 | CAATT | C | 5 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(2): Show |
5 | HG00323.hp2 HG01358.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.343+541_343+544del others(4): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90561077 | |||||||
| chr6:90561468 | C | T | 4 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0174 others(1): Show |
4 | NA18939.hp2 NA18948.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.343+154G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90561468 | |||||||
| chr6:90561556 | G | A | 2 | a0001c0001t0007g0130 a0001c0001t0007g0131 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.343+66C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90561556 | |||||||
| chr6:90561613 | G | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0198 a0001c0001t0001g0233 others(2): Show |
8 | HG02129.hp1 NA18612.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.343+9C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90561613 | |||||||
| chr6:90561758 | T | C | 1 | a0001c0001t0005g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.298-91A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90561758 | |||||||
| chr6:90561808 | G | A | 1 | a0001c0001t0005g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.298-141C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90561808 | |||||||
| chr6:90561828 | G | A | 13 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0252 others(10): Show |
14 | HG01884.hp1 HG02451.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.298-161C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90561828 | |||||||
| chr6:90561859 | C | T | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.298-192G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90561859 | |||||||
| chr6:90562005 | C | T | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0215 |
3 | HG02109.hp2 HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.298-338G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562005 | |||||||
| chr6:90562126 | T | C | 1 | a0001c0001t0002g0111 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.298-459A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562126 | |||||||
| chr6:90562156 | G | A | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.298-489C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562156 | |||||||
| chr6:90562162 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.298-495C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562162 | |||||||
| chr6:90562278 | C | T | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.298-611G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562278 | |||||||
| chr6:90562361 | G | C | 1 | a0001c0001t0002g0022 | 2 | HG02056.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.298-694C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562361 | |||||||
| chr6:90562394 | C | T | 16 | a0001c0001t0004g0004 a0001c0001t0004g0027 a0001c0001t0004g0028 others(13): Show |
24 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.298-727G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562394 | |||||||
| chr6:90562438 | G | A | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.298-771C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562438 | |||||||
| chr6:90562446 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0192 a0001c0001t0001g0193 others(2): Show |
7 | HG00733.hp1 HG01192.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-779C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562446 | |||||||
| chr6:90562641 | C | G | 1 | a0001c0001t0001g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.298-974G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562641 | |||||||
| chr6:90563075 | T | C | 4 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0123 others(1): Show |
6 | HG01109.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-1408A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563075 | |||||||
| chr6:90563108 | C | A | 1 | a0001c0001t0007g0186 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.298-1441G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563108 | |||||||
| chr6:90563188 | G | A | 1 | a0001c0001t0005g0062 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.298-1521C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563188 | |||||||
| chr6:90563279 | C | A | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.298-1612G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563279 | |||||||
| chr6:90563456 | G | A | 1 | a0001c0001t0016g0046 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.298-1789C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563456 | |||||||
| chr6:90563521 | A | G | 8 | a0001c0001t0007g0031 a0001c0001t0007g0130 a0001c0001t0007g0131 others(5): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.298-1854T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563521 | |||||||
| chr6:90563543 | A | C | 36 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(33): Show |
42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.298-1876T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563543 | |||||||
| chr6:90563618 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.298-1951T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563618 | |||||||
| chr6:90563627 | C | T | 2 | a0001c0001t0009g0125 a0001c0001t0009g0127 |
2 | HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.298-1960G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563627 | |||||||
| chr6:90563671 | C | T | 2 | a0001c0001t0003g0165 a0001c0001t0003g0169 |
2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.298-2004G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563671 | |||||||
| chr6:90563734 | C | T | 1 | a0001c0001t0005g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.298-2067G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563734 | |||||||
| chr6:90563736 | C | T | 3 | a0001c0001t0003g0153 a0001c0001t0003g0163 a0001c0001t0003g0172 |
3 | HG00609.hp1 NA19075.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.298-2069G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563736 | |||||||
| chr6:90564133 | A | G | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.298-2466T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564133 | |||||||
| chr6:90564211 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.298-2544G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564211 | |||||||
| chr6:90564216 | C | T | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.298-2549G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564216 | |||||||
| chr6:90564284 | G | C | 36 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(33): Show |
42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.298-2617C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564284 | |||||||
| chr6:90564288 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.298-2621C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564288 | |||||||
| chr6:90564383 | G | C | 1 | a0001c0001t0001g0242 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.298-2716C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564383 | |||||||
| chr6:90564588 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.298-2921G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564588 | |||||||
| chr6:90564816 | G | A | 2 | a0001c0001t0007g0080 a0001c0001t0013g0069 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.298-3149C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564816 | |||||||
| chr6:90564926 | C | G | 1 | a0001c0001t0002g0107 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.298-3259G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564926 | |||||||
| chr6:90564927 | A | G | 1 | a0001c0001t0002g0107 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.298-3260T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564927 | |||||||
| chr6:90565115 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.297+3443A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565115 | |||||||
| chr6:90565119 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.297+3439T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565119 | |||||||
| chr6:90565248 | CA | C | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+3309delT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565248 | |||||||
| chr6:90565333 | A | G | 1 | a0001c0001t0009g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.297+3225T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565333 | |||||||
| chr6:90565358 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.297+3200G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565358 | |||||||
| chr6:90565415 | T | C | 5 | a0001c0001t0009g0091 a0001c0001t0009g0110 a0001c0001t0009g0125 others(2): Show |
5 | HG00733.hp2 HG02451.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+3143A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565415 | |||||||
| chr6:90565493 | C | A | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.297+3065G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565493 | |||||||
| chr6:90565557 | TG | T | 21 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(18): Show |
23 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.297+3000delC | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565557 | |||||||
| chr6:90565618 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.297+2940C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565618 | |||||||
| chr6:90565676 | C | T | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.297+2882G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565676 | |||||||
| chr6:90565797 | C | T | 2 | a0001c0002t0004g0115 a0001c0002t0004g0129 |
2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.297+2761G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565797 | |||||||
| chr6:90565798 | G | A | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.297+2760C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565798 | |||||||
| chr6:90565800 | T | C | 1 | a0001c0001t0002g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.297+2758A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565800 | |||||||
| chr6:90565953 | T | C | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+2605A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565953 | |||||||
| chr6:90566171 | A | G | 172 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0001g0207 others(169): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.297+2387T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566171 | |||||||
| chr6:90566263 | G | T | 86 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(83): Show |
120 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.297+2295C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566263 | |||||||
| chr6:90566287 | T | C | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.297+2271A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566287 | |||||||
| chr6:90566460 | C | T | 2 | a0001c0001t0003g0250 a0001c0001t0003g0251 |
2 | HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.297+2098G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566460 | |||||||
| chr6:90566576 | T | G | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+1982A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566576 | |||||||
| chr6:90566586 | T | C | 2 | a0001c0001t0002g0107 a0001c0001t0002g0111 |
2 | NA19001.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.297+1972A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566586 | |||||||
| chr6:90566747 | A | G | 10 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0056 others(7): Show |
16 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.297+1811T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566747 | |||||||
| chr6:90566748 | T | G | 1 | a0001c0001t0002g0084 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.297+1810A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566748 | |||||||
| chr6:90566810 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.297+1748G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566810 | |||||||
| chr6:90566816 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.297+1742A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566816 | |||||||
| chr6:90566843 | C | T | 19 | a0001c0001t0004g0004 a0001c0001t0004g0027 a0001c0001t0004g0028 others(16): Show |
28 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.297+1715G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566843 | |||||||
| chr6:90566871 | A | G | 1 | a0001c0001t0012g0021 | 2 | HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.297+1687T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566871 | |||||||
| chr6:90566989 | C | T | 1 | a0001c0001t0003g0153 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.297+1569G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566989 | |||||||
| chr6:90567011 | T | C | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.297+1547A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567011 | |||||||
| chr6:90567103 | A | G | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.297+1455T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567103 | |||||||
| chr6:90567273 | C | G | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+1285G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567273 | |||||||
| chr6:90567302 | G | A | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+1256C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567302 | |||||||
| chr6:90567382 | C | A | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.297+1176G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567382 | |||||||
| chr6:90567457 | G | T | 57 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(54): Show |
70 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.297+1101C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567457 | |||||||
| chr6:90567585 | G | C | 1 | a0001c0001t0003g0153 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.297+973C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567585 | |||||||
| chr6:90567608 | C | T | 168 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0001g0242 others(165): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.297+950G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567608 | |||||||
| chr6:90567717 | A | G | 21 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(18): Show |
23 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.297+841T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567717 | |||||||
| chr6:90567786 | C | G | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+772G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567786 | |||||||
| chr6:90567969 | A | C | 1 | a0001c0001t0003g0172 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.297+589T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567969 | |||||||
| chr6:90567980 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.297+578T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567980 | |||||||
| chr6:90568085 | G | C | 1 | a0001c0001t0002g0092 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.297+473C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90568085 | |||||||
| chr6:90568087 | TA | T | 167 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(164): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.297+470delT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90568087 | |||||||
| chr6:90568297 | G | A | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.297+261C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90568297 | |||||||
| chr6:90568314 | AT | A | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.297+243delA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90568314 | |||||||
| chr6:90568450 | T | C | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02109.hp2 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+108A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90568450 | |||||||
| chr6:90568467 | AC | A | 4 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0004g0093 others(1): Show |
4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+90delG | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90568467 | |||||||
| chr6:90568701 | T | C | 36 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(33): Show |
42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.232-78A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90568701 | |||||||
| chr6:90568703 | T | C | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.232-80A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90568703 | |||||||
| chr6:90568796 | C | T | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.232-173G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90568796 | |||||||
| chr6:90568832 | C | G | 86 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(83): Show |
120 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.232-209G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90568832 | |||||||
| chr6:90568949 | C | T | 44 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(41): Show |
51 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.232-326G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90568949 | |||||||
| chr6:90569067 | G | A | 18 | a0001c0001t0004g0004 a0001c0001t0004g0027 a0001c0001t0004g0028 others(15): Show |
26 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.232-444C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90569067 | |||||||
| chr6:90569259 | AC | A | 5 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(2): Show |
5 | HG00323.hp2 HG01358.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-637delG | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90569259 | |||||||
| chr6:90569406 | G | C | 64 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0013 others(61): Show |
90 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.232-783C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90569406 | |||||||
| chr6:90569475 | ACTT | A | 10 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0056 others(7): Show |
16 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.232-855_232-853del others(3): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90569475 | |||||||
| chr6:90569476 | C | CTTCT | 34 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(31): Show |
39 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.232-857_232-854dup others(4): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90569476 | |||||||
| chr6:90569635 | T | C | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02109.hp2 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.232-1012A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90569635 | |||||||
| chr6:90569752 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.232-1129C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90569752 | |||||||
| chr6:90570001 | T | C | 4 | a0001c0001t0003g0048 a0001c0001t0003g0050 a0001c0001t0003g0052 others(1): Show |
4 | HG00323.hp2 HG01358.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.232-1378A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570001 | |||||||
| chr6:90570002 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.232-1379G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570002 | |||||||
| chr6:90570014 | G | T | 22 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(19): Show |
24 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.232-1391C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570014 | |||||||
| chr6:90570193 | T | A | 1 | a0001c0001t0001g0256 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.231+1504A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570193 | |||||||
| chr6:90570204 | C | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.231+1493G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570204 | |||||||
| chr6:90570217 | C | T | 21 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(18): Show |
23 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.231+1480G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570217 | |||||||
| chr6:90570390 | G | A | 36 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(33): Show |
42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.231+1307C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570390 | |||||||
| chr6:90570582 | T | C | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.231+1115A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570582 | |||||||
| chr6:90570656 | A | G | 2 | a0001c0001t0005g0063 a0001c0001t0005g0064 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.231+1041T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570656 | |||||||
| chr6:90570809 | T | C | 18 | a0001c0001t0004g0004 a0001c0001t0004g0027 a0001c0001t0004g0028 others(15): Show |
26 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.231+888A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570809 | |||||||
| chr6:90570837 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.231+860A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570837 | |||||||
| chr6:90570946 | T | G | 1 | a0001c0001t0001g0223 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.231+751A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570946 | |||||||
| chr6:90571082 | C | G | 1 | a0001c0001t0002g0014 | 3 | HG01099.hp2 HG01952.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.231+615G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90571082 | |||||||
| chr6:90571089 | C | G | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.231+608G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90571089 | |||||||
| chr6:90571497 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0004g0093 others(1): Show |
4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+200G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90571497 | |||||||
| chr6:90571632 | TA | T | 13 | a0001c0001t0002g0013 a0001c0001t0002g0015 a0001c0001t0002g0032 others(10): Show |
19 | HG00558.hp1 HG01069.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.231+64delT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90571632 | |||||||
| chr6:90571915 | TA | T | 160 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0001g0239 others(157): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.121-109delT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90571915 | |||||||
| chr6:90571983 | A | G | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.121-176T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90571983 | |||||||
| chr6:90572187 | T | C | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.121-380A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572187 | |||||||
| chr6:90572254 | G | A | 2 | a0001c0001t0005g0063 a0001c0001t0005g0064 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.121-447C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572254 | |||||||
| chr6:90572270 | C | T | 8 | a0001c0001t0007g0031 a0001c0001t0007g0130 a0001c0001t0007g0131 others(5): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-463G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572270 | |||||||
| chr6:90572402 | T | G | 1 | a0001c0001t0006g0135 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.121-595A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572402 | |||||||
| chr6:90572536 | G | A | 1 | a0001c0001t0003g0179 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.121-729C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572536 | |||||||
| chr6:90572569 | T | TA | 15 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(12): Show |
21 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.121-763dupT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572569 | |||||||
| chr6:90572569 | T | TAA | 21 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(18): Show |
23 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.121-764_121-763dup others(2): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572569 | |||||||
| chr6:90572582 | C | A | 1 | a0001c0001t0007g0130 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.121-775G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572582 | |||||||
| chr6:90572685 | C | G | 2 | a0001c0001t0002g0083 a0001c0001t0002g0084 |
2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.121-878G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572685 | |||||||
| chr6:90572717 | A | C | 2 | a0001c0001t0004g0205 a0001c0001t0004g0217 |
2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.121-910T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572717 | |||||||
| chr6:90572738 | T | C | 1 | a0001c0001t0007g0155 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.121-931A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572738 | |||||||
| chr6:90572770 | A | G | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.121-963T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572770 | |||||||
| chr6:90572993 | G | C | 1 | a0001c0001t0016g0046 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.121-1186C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572993 | |||||||
| chr6:90573253 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.121-1446C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573253 | |||||||
| chr6:90573344 | T | C | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.121-1537A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573344 | |||||||
| chr6:90573347 | A | G | 2 | a0001c0001t0002g0082 a0001c0001t0002g0096 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.121-1540T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573347 | |||||||
| chr6:90573415 | TTAA | T | 8 | a0001c0001t0007g0031 a0001c0001t0007g0130 a0001c0001t0007g0131 others(5): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-1611_121-1609d others(5): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573415 | |||||||
| chr6:90573452 | C | T | 36 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(33): Show |
42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.121-1645G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573452 | |||||||
| chr6:90573645 | G | C | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | NA18955.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.121-1838C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573645 | |||||||
| chr6:90573665 | T | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0216 a0001c0001t0001g0224 |
4 | HG00408.hp1 HG02027.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-1858A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573665 | |||||||
| chr6:90573707 | G | A | 1 | a0001c0001t0006g0139 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.121-1900C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573707 | |||||||
| chr6:90573822 | G | A | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.121-2015C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573822 | |||||||
| chr6:90573854 | G | A | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.121-2047C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573854 | |||||||
| chr6:90573969 | T | C | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.121-2162A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573969 | |||||||
| chr6:90574121 | G | A | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.121-2314C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574121 | |||||||
| chr6:90574222 | T | C | 4 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0004g0093 others(1): Show |
4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-2415A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574222 | |||||||
| chr6:90574350 | C | T | 1 | a0001c0001t0003g0181 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.121-2543G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574350 | |||||||
| chr6:90574477 | T | C | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.121-2670A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574477 | |||||||
| chr6:90574531 | T | A | 1 | a0001c0001t0004g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.121-2724A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574531 | |||||||
| chr6:90574546 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.121-2739G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574546 | |||||||
| chr6:90574607 | G | A | 23 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(20): Show |
25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.121-2800C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574607 | |||||||
| chr6:90574723 | C | T | 1 | a0001c0001t0003g0171 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.121-2916G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574723 | |||||||
| chr6:90575113 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0054 |
3 | NA18939.hp1 NA18961.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.121-3306C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90575113 | |||||||
| chr6:90575145 | T | C | 1 | a0001c0001t0003g0180 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.121-3338A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90575145 | |||||||
| chr6:90575271 | T | G | 86 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(83): Show |
120 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.121-3464A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90575271 | |||||||
| chr6:90575610 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.121-3803A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90575610 | |||||||
| chr6:90575730 | C | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0004g0094 |
3 | HG01496.hp1 HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.121-3923G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90575730 | |||||||
| chr6:90576177 | A | G | 5 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(2): Show |
5 | HG00323.hp2 HG01358.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-4370T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576177 | |||||||
| chr6:90576205 | C | T | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.121-4398G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576205 | |||||||
| chr6:90576209 | G | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0004g0094 |
3 | HG01496.hp1 HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.121-4402C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576209 | |||||||
| chr6:90576418 | G | GTC | 5 | a0001c0001t0002g0032 a0001c0001t0002g0111 a0001c0001t0002g0113 others(2): Show |
7 | HG01975.hp2 HG02074.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.121-4613_121-4612d others(4): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576418 | |||||||
| chr6:90576419 | T | TCA | 15 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0041 others(12): Show |
22 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.121-4614_121-4613d others(4): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | |||||||
| chr6:90576419 | T | TCACA | 5 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01168.hp1 HG01261.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-4616_121-4613d others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | |||||||
| chr6:90576419 | T | TCACACA | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0245 |
3 | HG03704.hp2 NA18963.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.121-4618_121-4613d others(8): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | |||||||
| chr6:90576419 | T | TCACACAC others(1): Show |
3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0018g0254 |
3 | HG02698.hp2 HG02922.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.121-4620_121-4613d others(10): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | |||||||
| chr6:90576419 | T | TCTCACAC others(3): Show |
2 | a0001c0001t0002g0074 a0001c0001t0002g0114 |
2 | HG01515.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.121-4613_121-4612i others(12): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | |||||||
| chr6:90576419 | TCA | T | 46 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0017 others(43): Show |
65 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.121-4614_121-4613d others(4): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | |||||||
| chr6:90576419 | TCACA | T | 55 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0076 others(52): Show |
78 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.121-4616_121-4613d others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | |||||||
| chr6:90576419 | TCACACA | T | 50 | a0001c0001t0001g0037 a0001c0001t0001g0187 a0001c0001t0001g0188 others(47): Show |
54 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.121-4618_121-4613d others(8): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | |||||||
| chr6:90576419 | TCACACAC others(1): Show |
T | 23 | a0001c0001t0003g0033 a0001c0001t0003g0034 a0001c0001t0003g0049 others(20): Show |
27 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.121-4620_121-4613d others(10): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | |||||||
| chr6:90576419 | TCACACAC others(3): Show |
T | 13 | a0001c0001t0003g0048 a0001c0001t0003g0052 a0001c0001t0003g0250 others(10): Show |
19 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.121-4622_121-4613d others(12): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | |||||||
| chr6:90576419 | TCACACAC others(5): Show |
T | 1 | a0001c0001t0003g0164 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.121-4624_121-4613d others(14): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | |||||||
| chr6:90576419 | TCACACAC others(11): Show |
T | 2 | a0001c0001t0004g0121 a0001c0001t0004g0122 |
2 | HG00741.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.121-4630_121-4613d others(20): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | |||||||
| chr6:90576419 | TCACACAC others(13): Show |
T | 11 | a0001c0001t0004g0004 a0001c0001t0004g0027 a0001c0001t0004g0028 others(8): Show |
17 | HG00735.hp1 HG00735.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.121-4632_121-4613d others(22): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | |||||||
| chr6:90576421 | A | T | 10 | a0001c0001t0002g0015 a0001c0001t0002g0026 a0001c0001t0002g0075 others(7): Show |
12 | HG01069.hp1 HG01516.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.121-4614T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576421 | |||||||
| chr6:90576423 | A | T | 18 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0072 others(15): Show |
23 | HG00099.hp1 HG00280.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.121-4616T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576423 | |||||||
| chr6:90576425 | A | T | 27 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0014 others(24): Show |
44 | HG00408.hp2 HG00597.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.121-4618T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576425 | |||||||
| chr6:90576427 | A | T | 23 | a0001c0001t0002g0013 a0001c0001t0002g0077 a0001c0001t0002g0079 others(20): Show |
26 | HG00280.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.121-4620T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576427 | |||||||
| chr6:90576429 | A | T | 13 | a0001c0001t0003g0033 a0001c0001t0003g0034 a0001c0001t0003g0049 others(10): Show |
15 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.121-4622T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576429 | |||||||
| chr6:90576431 | A | G | 1 | a0001c0001t0005g0058 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.121-4624T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576431 | |||||||
| chr6:90576431 | A | T | 2 | a0001c0001t0003g0048 a0001c0001t0003g0052 |
2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.121-4624T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576431 | |||||||
| chr6:90576432 | C | G | 1 | a0001c0001t0005g0058 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.121-4625G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576432 | |||||||
| chr6:90576433 | A | T | 1 | a0001c0001t0003g0164 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.121-4626T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576433 | |||||||
| chr6:90576461 | ACACACAC others(4): Show |
A | 1 | a0001c0001t0009g0127 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.121-4665_121-4655d others(13): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576461 | |||||||
| chr6:90576715 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.121-4908G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576715 | |||||||
| chr6:90576851 | G | T | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.121-5044C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576851 | |||||||
| chr6:90577026 | G | A | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.121-5219C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90577026 | |||||||
| chr6:90577175 | A | T | 1 | a0001c0001t0002g0075 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.121-5368T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90577175 | |||||||
| chr6:90577470 | CAGTTGGA others(17): Show |
C | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.121-5687_121-5664d others(26): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90577470 | |||||||
| chr6:90577496 | T | A | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.121-5689A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90577496 | |||||||
| chr6:90577750 | T | C | 1 | a0001c0001t0001g0241 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.121-5943A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90577750 | |||||||
| chr6:90577936 | G | A | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.121-6129C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90577936 | |||||||
| chr6:90577960 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.121-6153A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90577960 | |||||||
| chr6:90578029 | G | A | 27 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(24): Show |
29 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.121-6222C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90578029 | |||||||
| chr6:90578054 | C | T | 1 | a0001c0001t0005g0056 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.121-6247G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90578054 | |||||||
| chr6:90578325 | T | G | 1 | a0001c0001t0006g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.121-6518A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90578325 | |||||||
| chr6:90578457 | T | C | 1 | a0001c0001t0003g0052 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.121-6650A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90578457 | |||||||
| chr6:90578463 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.121-6656G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90578463 | |||||||
| chr6:90578503 | G | C | 1 | a0001c0001t0003g0183 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.121-6696C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90578503 | |||||||
| chr6:90578950 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.121-7143G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90578950 | |||||||
| chr6:90579020 | T | C | 16 | a0001c0001t0004g0004 a0001c0001t0004g0027 a0001c0001t0004g0028 others(13): Show |
24 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.121-7213A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579020 | |||||||
| chr6:90579084 | G | C | 25 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(22): Show |
27 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.121-7277C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579084 | |||||||
| chr6:90579296 | T | C | 1 | a0001c0001t0003g0170 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.120+7468A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579296 | |||||||
| chr6:90579369 | A | G | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.120+7395T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579369 | |||||||
| chr6:90579376 | C | T | 36 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(33): Show |
42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.120+7388G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579376 | |||||||
| chr6:90579469 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.120+7295G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579469 | |||||||
| chr6:90579470 | T | C | 18 | a0001c0001t0004g0004 a0001c0001t0004g0027 a0001c0001t0004g0028 others(15): Show |
26 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.120+7294A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579470 | |||||||
| chr6:90579635 | A | C | 25 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(22): Show |
27 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.120+7129T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579635 | |||||||
| chr6:90579800 | C | T | 27 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(24): Show |
29 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.120+6964G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579800 | |||||||
| chr6:90579904 | G | C | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.120+6860C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579904 | |||||||
| chr6:90579961 | A | G | 2 | a0001c0001t0007g0154 a0001c0001t0007g0155 |
2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.120+6803T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579961 | |||||||
| chr6:90580009 | T | A | 4 | a0001c0001t0006g0145 a0001c0001t0006g0147 a0001c0001t0006g0148 others(1): Show |
4 | HG02027.hp1 HG02080.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+6755A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90580009 | |||||||
| chr6:90580165 | A | G | 36 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(33): Show |
42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.120+6599T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90580165 | |||||||
| chr6:90580610 | G | A | 15 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0056 others(12): Show |
21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.120+6154C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90580610 | |||||||
| chr6:90580619 | C | A | 36 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(33): Show |
42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.120+6145G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90580619 | |||||||
| chr6:90580716 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.120+6048G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90580716 | |||||||
| chr6:90580861 | T | C | 4 | a0001c0001t0007g0130 a0001c0001t0007g0131 a0001c0001t0007g0132 others(1): Show |
4 | HG02145.hp1 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+5903A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90580861 | |||||||
| chr6:90580913 | C | A | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | NA18955.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.120+5851G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90580913 | |||||||
| chr6:90581148 | C | T | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.120+5616G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90581148 | |||||||
| chr6:90581433 | C | G | 86 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(83): Show |
120 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.120+5331G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90581433 | |||||||
| chr6:90581597 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.120+5167G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90581597 | |||||||
| chr6:90581743 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.120+5021T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90581743 | |||||||
| chr6:90581815 | A | G | 39 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(36): Show |
46 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.120+4949T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90581815 | |||||||
| chr6:90581840 | C | T | 2 | a0001c0001t0002g0072 a0001c0001t0002g0073 |
2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.120+4924G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90581840 | |||||||
| chr6:90581992 | T | C | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.120+4772A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90581992 | |||||||
| chr6:90582043 | G | A | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.120+4721C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582043 | |||||||
| chr6:90582083 | C | T | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.120+4681G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582083 | |||||||
| chr6:90582101 | T | C | 1 | a0001c0001t0021g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.120+4663A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582101 | |||||||
| chr6:90582148 | ATCTGGCC others(3): Show |
A | 1 | a0001c0001t0005g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.120+4606_120+4615d others(12): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582148 | |||||||
| chr6:90582150 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.120+4614G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582150 | |||||||
| chr6:90582604 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.120+4160G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582604 | |||||||
| chr6:90582609 | T | C | 18 | a0001c0001t0003g0007 a0001c0001t0003g0035 a0001c0001t0003g0153 others(15): Show |
22 | HG00280.hp1 HG00609.hp1 HG02165.hp2 others(19): Show |
intron_variant | MODIFIER | c.120+4155A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582609 | |||||||
| chr6:90582678 | CAAA | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
5 | HG01169.hp1 HG02080.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+4083_120+4085d others(5): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582678 | |||||||
| chr6:90582880 | C | CT | 33 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0262 others(30): Show |
36 | HG00099.hp2 HG00597.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.120+3883dupA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582880 | |||||||
| chr6:90582880 | CT | C | 8 | a0001c0001t0001g0193 a0001c0001t0001g0244 a0001c0001t0001g0245 others(5): Show |
8 | HG00323.hp1 HG01074.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.120+3883delA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582880 | |||||||
| chr6:90582917 | C | T | 86 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(83): Show |
120 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.120+3847G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582917 | |||||||
| chr6:90582937 | C | T | 1 | a0001c0001t0003g0163 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.120+3827G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582937 | |||||||
| chr6:90583407 | C | G | 1 | a0001c0001t0016g0046 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.120+3357G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90583407 | |||||||
| chr6:90583423 | C | T | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.120+3341G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90583423 | |||||||
| chr6:90584205 | T | A | 3 | a0001c0001t0007g0031 a0001c0001t0007g0154 a0001c0001t0007g0155 |
4 | HG01884.hp2 HG02257.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2559A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90584205 | |||||||
| chr6:90584288 | T | G | 1 | a0001c0001t0001g0188 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.120+2476A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90584288 | |||||||
| chr6:90584383 | T | C | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.120+2381A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90584383 | |||||||
| chr6:90584534 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.120+2230A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90584534 | |||||||
| chr6:90584582 | G | A | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.120+2182C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90584582 | |||||||
| chr6:90584801 | A | G | 12 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0252 others(9): Show |
13 | HG01884.hp1 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.120+1963T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90584801 | |||||||
| chr6:90584971 | T | C | 2 | a0001c0001t0003g0184 a0001c0001t0003g0185 |
2 | HG01074.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.120+1793A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90584971 | |||||||
| chr6:90585074 | T | G | 1 | a0001c0002t0004g0129 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.120+1690A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585074 | |||||||
| chr6:90585138 | C | T | 25 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(22): Show |
27 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.120+1626G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585138 | |||||||
| chr6:90585285 | TTCTC | T | 26 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(23): Show |
28 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.120+1475_120+1478d others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585285 | |||||||
| chr6:90585320 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1444T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585320 | |||||||
| chr6:90585321 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1443T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585321 | |||||||
| chr6:90585322 | C | A | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.120+1442G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585322 | |||||||
| chr6:90585322 | C | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1442G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585322 | |||||||
| chr6:90585323 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1441T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585323 | |||||||
| chr6:90585324 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0194 a0001c0001t0001g0195 |
5 | HG00733.hp1 HG01192.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+1440A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585324 | |||||||
| chr6:90585325 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1439T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585325 | |||||||
| chr6:90585327 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1437T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585327 | |||||||
| chr6:90585330 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1434T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585330 | |||||||
| chr6:90585333 | C | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1431G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585333 | |||||||
| chr6:90585334 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1430T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585334 | |||||||
| chr6:90585335 | G | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1429C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585335 | |||||||
| chr6:90585337 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1427T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585337 | |||||||
| chr6:90585338 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1426T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585338 | |||||||
| chr6:90585340 | C | A | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1424G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585340 | |||||||
| chr6:90585341 | C | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1423G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585341 | |||||||
| chr6:90585342 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1422T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585342 | |||||||
| chr6:90585345 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1419T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585345 | |||||||
| chr6:90585346 | C | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1418G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585346 | |||||||
| chr6:90585348 | C | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1416G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585348 | |||||||
| chr6:90585351 | C | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1413G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585351 | |||||||
| chr6:90585352 | C | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1412G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585352 | |||||||
| chr6:90585353 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1411T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585353 | |||||||
| chr6:90585354 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1410T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585354 | |||||||
| chr6:90585355 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1409T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585355 | |||||||
| chr6:90585356 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1408T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585356 | |||||||
| chr6:90585357 | C | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1407G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585357 | |||||||
| chr6:90585358 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1406T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585358 | |||||||
| chr6:90585360 | G | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1404C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585360 | |||||||
| chr6:90585361 | C | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1403G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585361 | |||||||
| chr6:90585362 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1402T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585362 | |||||||
| chr6:90585363 | C | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1401G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585363 | |||||||
| chr6:90585364 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1400T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585364 | |||||||
| chr6:90585365 | G | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1399C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585365 | |||||||
| chr6:90585366 | G | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1398C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585366 | |||||||
| chr6:90585367 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1397T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585367 | |||||||
| chr6:90585368 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1396T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585368 | |||||||
| chr6:90585369 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1395T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585369 | |||||||
| chr6:90585370 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1394T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585370 | |||||||
| chr6:90585371 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1393T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585371 | |||||||
| chr6:90585372 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1392T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585372 | |||||||
| chr6:90585373 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1391T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585373 | |||||||
| chr6:90585374 | A | T | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1390T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585374 | |||||||
| chr6:90585600 | A | ATATATAT others(151): Show |
1 | a0001c0001t0007g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.120+1163_120+1164i others(160): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585600 | |||||||
| chr6:90585600 | A | ATATATAT others(152): Show |
1 | a0001c0001t0007g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.120+1163_120+1164i others(161): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585600 | |||||||
| chr6:90585600 | A | ATATATAT others(169): Show |
1 | a0001c0001t0007g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.120+1163_120+1164i others(178): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585600 | |||||||
| chr6:90585600 | A | ATATATAT others(180): Show |
1 | a0001c0001t0007g0130 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.120+1163_120+1164i others(189): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585600 | |||||||
| chr6:90585729 | G | GA | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0055 others(10): Show |
19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.120+1034dupT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585729 | |||||||
| chr6:90585742 | T | C | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.120+1022A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585742 | |||||||
| chr6:90585976 | T | C | 1 | a0001c0001t0023g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.120+788A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585976 | |||||||
| chr6:90586054 | T | C | 28 | a0001c0001t0004g0066 a0001c0001t0004g0137 a0001c0001t0004g0138 others(25): Show |
30 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.120+710A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586054 | |||||||
| chr6:90586095 | G | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.120+669C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586095 | |||||||
| chr6:90586099 | C | G | 166 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(163): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.120+665G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586099 | |||||||
| chr6:90586245 | G | C | 39 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0034 others(36): Show |
46 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.120+519C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586245 | |||||||
| chr6:90586265 | G | A | 86 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(83): Show |
120 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.120+499C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586265 | |||||||
| chr6:90586358 | G | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0192 a0001c0001t0001g0193 others(2): Show |
7 | HG00733.hp1 HG01192.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+406C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586358 | |||||||
| chr6:90586378 | C | CA | 34 | a0001c0001t0001g0262 a0001c0001t0001g0264 a0001c0001t0003g0007 others(31): Show |
40 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.120+385dupT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586378 | |||||||
| chr6:90586378 | CA | C | 168 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(165): Show |
237 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.120+385delT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586378 | |||||||
| chr6:90586378 | CAA | C | 10 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(7): Show |
10 | HG00323.hp2 HG01243.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.120+384_120+385del others(2): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586378 | |||||||
| chr6:90586378 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0007g0186 |
3 | HG02630.hp1 HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.120+376_120+385del others(10): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586378 | |||||||
| chr6:90586413 | C | T | 1 | a0001c0001t0022g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.120+351G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586413 | |||||||
| chr6:90586701 | C | G | 166 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0002g0001 others(163): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.120+63G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586701 |