Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4214 |
| ensemblid | ENSG00000095015.6 |
| hgncid | 6848 |
| symbol | MAP3K1 |
| name | mitogen-activated protein kinase kinase kinase 1 |
| refseq_nuc | NM_005921.2 |
| refseq_prot | NP_005912.1 |
| ensembl_nuc | ENST00000399503.4 |
| ensembl_prot | ENSP00000382423.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 56815549 |
| end | 56896152 |
| strand | + |
| ver | v1.2 |
| region | chr5:56815549-56896152 |
| region5000 | chr5:56810549-56901152 |
| regionname0 | MAP3K1_chr5_56815549_56896152 |
| regionname5000 | MAP3K1_chr5_56810549_56901152 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1511 | 149 | 42 | 30 | 51 | 8 | 18 | 42 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | MAAAA others(1506): Show |
chr5 | 56810549 | 56901152 |
| a0002 | 1/0 | 1512 | 133 | 20 | 25 | 73 | 2 | 12 | 54 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | MAAAA others(1507): Show |
chr5 | 56810549 | 56901152 |
| a0003 | 0/0 | 1511 | 86 | 18 | 9 | 44 | 2 | 13 | 33 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | MAAAA others(1506): Show |
chr5 | 56810549 | 56901152 |
| a0004 | 0/0 | 1511 | 4 | 0 | 3 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | MAAAA others(1506): Show |
chr5 | 56810549 | 56901152 |
| a0005 | 0/0 | 1511 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | MAAAA others(1506): Show |
chr5 | 56810549 | 56901152 |
| a0006 | 0/1 | 1511 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | MAAAA others(1506): Show |
chr5 | 56810549 | 56901152 |
| a0007 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | MAAAA others(1507): Show |
chr5 | 56810549 | 56901152 |
| a0008 | 0/0 | 1511 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | MAAAA others(1506): Show |
chr5 | 56810549 | 56901152 |
| a0009 | 0/0 | 1511 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | MAAAA others(1506): Show |
chr5 | 56810549 | 56901152 |
| a0010 | 0/0 | 1512 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | MAAAA others(1507): Show |
chr5 | 56810549 | 56901152 |
| a0011 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | MAAAA others(1507): Show |
chr5 | 56810549 | 56901152 |
| a0012 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | MAAAA others(1507): Show |
chr5 | 56810549 | 56901152 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4533 | 93 | 26 | 26 | 21 | 6 | 14 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4528): Show |
chr5 | 56810549 | 56901152 | ||
| a0001c0005 | 0/0 | 4533 | 26 | 5 | 0 | 18 | 0 | 3 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4528): Show |
chr5 | 56810549 | 56901152 | ||
| a0001c0006 | 0/0 | 4533 | 21 | 3 | 3 | 12 | 2 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4528): Show |
chr5 | 56810549 | 56901152 | ||
| a0001c0008 | 0/0 | 4533 | 5 | 5 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4528): Show |
chr5 | 56810549 | 56901152 | ||
| a0001c0011 | 0/0 | 4533 | 4 | 3 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4528): Show |
chr5 | 56810549 | 56901152 | ||
| a0002c0003 | 1/0 | 4536 | 80 | 16 | 10 | 47 | 1 | 5 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4531): Show |
chr5 | 56810549 | 56901152 | ||
| a0002c0004 | 0/0 | 4536 | 45 | 3 | 8 | 26 | 1 | 7 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4531): Show |
chr5 | 56810549 | 56901152 | ||
| a0002c0007 | 0/0 | 4536 | 8 | 1 | 7 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4531): Show |
chr5 | 56810549 | 56901152 | ||
| a0003c0002 | 0/0 | 4533 | 82 | 15 | 8 | 44 | 2 | 13 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4528): Show |
chr5 | 56810549 | 56901152 | ||
| a0003c0009 | 0/0 | 4533 | 4 | 3 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4528): Show |
chr5 | 56810549 | 56901152 | ||
| a0004c0010 | 0/0 | 4533 | 4 | 0 | 3 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4528): Show |
chr5 | 56810549 | 56901152 | ||
| a0005c0012 | 0/0 | 4533 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4528): Show |
chr5 | 56810549 | 56901152 | ||
| a0005c0015 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4528): Show |
chr5 | 56810549 | 56901152 | ||
| a0006c0013 | 0/1 | 4533 | 2 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4528): Show |
chr5 | 56810549 | 56901152 | ||
| a0007c0020 | 0/0 | 4536 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4531): Show |
chr5 | 56810549 | 56901152 | ||
| a0008c0017 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4528): Show |
chr5 | 56810549 | 56901152 | ||
| a0009c0016 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4528): Show |
chr5 | 56810549 | 56901152 | ||
| a0010c0014 | 0/0 | 4536 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4531): Show |
chr5 | 56810549 | 56901152 | ||
| a0011c0018 | 0/0 | 4536 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4531): Show |
chr5 | 56810549 | 56901152 | ||
| a0012c0019 | 0/0 | 4536 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | ATGGC others(4531): Show |
chr5 | 56810549 | 56901152 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 7034 | 68 | 11 | 25 | 13 | 6 | 13 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7029): Show |
chr5 | 56810549 | 56901152 |
| a0001c0001t0007 | 0/0 | 7035 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7030): Show |
chr5 | 56810549 | 56901152 |
| a0001c0001t0008 | 0/0 | 7035 | 9 | 3 | 0 | 6 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7030): Show |
chr5 | 56810549 | 56901152 |
| a0001c0001t0009 | 0/0 | 7034 | 9 | 9 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7029): Show |
chr5 | 56810549 | 56901152 |
| a0001c0001t0010 | 0/0 | 7033 | 3 | 1 | 1 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7028): Show |
chr5 | 56810549 | 56901152 |
| a0001c0001t0011 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7028): Show |
chr5 | 56810549 | 56901152 |
| a0001c0001t0015 | 0/0 | 7034 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7029): Show |
chr5 | 56810549 | 56901152 |
| a0001c0001t0017 | 0/0 | 7034 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7029): Show |
chr5 | 56810549 | 56901152 |
| a0001c0005t0001 | 0/0 | 7033 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7028): Show |
chr5 | 56810549 | 56901152 |
| a0001c0005t0003 | 0/0 | 7035 | 18 | 0 | 0 | 16 | 0 | 2 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7030): Show |
chr5 | 56810549 | 56901152 |
| a0001c0005t0004 | 0/0 | 7034 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7029): Show |
chr5 | 56810549 | 56901152 |
| a0001c0005t0007 | 0/0 | 7035 | 5 | 5 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7030): Show |
chr5 | 56810549 | 56901152 |
| a0001c0005t0013 | 0/0 | 7035 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7030): Show |
chr5 | 56810549 | 56901152 |
| a0001c0006t0001 | 0/0 | 7033 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7028): Show |
chr5 | 56810549 | 56901152 |
| a0001c0006t0003 | 0/0 | 7035 | 16 | 3 | 2 | 8 | 2 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7030): Show |
chr5 | 56810549 | 56901152 |
| a0001c0006t0004 | 0/0 | 7034 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7029): Show |
chr5 | 56810549 | 56901152 |
| a0001c0008t0007 | 0/0 | 7035 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7030): Show |
chr5 | 56810549 | 56901152 |
| a0001c0008t0011 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7028): Show |
chr5 | 56810549 | 56901152 |
| a0001c0011t0007 | 0/0 | 7035 | 4 | 3 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7030): Show |
chr5 | 56810549 | 56901152 |
| a0002c0003t0001 | 0/0 | 7036 | 44 | 15 | 5 | 19 | 1 | 4 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7031): Show |
chr5 | 56810549 | 56901152 |
| a0002c0003t0004 | 0/0 | 7037 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7032): Show |
chr5 | 56810549 | 56901152 |
| a0002c0003t0005 | 1/0 | 7036 | 21 | 0 | 2 | 18 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7031): Show |
chr5 | 56810549 | 56901152 |
| a0002c0003t0006 | 0/0 | 7035 | 8 | 0 | 2 | 6 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7030): Show |
chr5 | 56810549 | 56901152 |
| a0002c0003t0012 | 0/0 | 7036 | 2 | 0 | 0 | 1 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7031): Show |
chr5 | 56810549 | 56901152 |
| a0002c0003t0016 | 0/0 | 7037 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7032): Show |
chr5 | 56810549 | 56901152 |
| a0002c0003t0019 | 0/0 | 7036 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7031): Show |
chr5 | 56810549 | 56901152 |
| a0002c0003t0020 | 0/0 | 7036 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7031): Show |
chr5 | 56810549 | 56901152 |
| a0002c0004t0001 | 0/0 | 7036 | 23 | 3 | 5 | 12 | 1 | 2 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7031): Show |
chr5 | 56810549 | 56901152 |
| a0002c0004t0003 | 0/0 | 7038 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7033): Show |
chr5 | 56810549 | 56901152 |
| a0002c0004t0004 | 0/0 | 7037 | 19 | 0 | 3 | 11 | 0 | 5 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7032): Show |
chr5 | 56810549 | 56901152 |
| a0002c0004t0005 | 0/0 | 7036 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7031): Show |
chr5 | 56810549 | 56901152 |
| a0002c0007t0001 | 0/0 | 7036 | 8 | 1 | 7 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7031): Show |
chr5 | 56810549 | 56901152 |
| a0003c0002t0001 | 0/0 | 7033 | 58 | 2 | 6 | 37 | 2 | 11 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7028): Show |
chr5 | 56810549 | 56901152 |
| a0003c0002t0003 | 0/0 | 7035 | 3 | 1 | 2 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7030): Show |
chr5 | 56810549 | 56901152 |
| a0003c0002t0004 | 0/0 | 7034 | 9 | 1 | 0 | 7 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7029): Show |
chr5 | 56810549 | 56901152 |
| a0003c0002t0006 | 0/0 | 7032 | 9 | 9 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7027): Show |
chr5 | 56810549 | 56901152 |
| a0003c0002t0007 | 0/0 | 7035 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7030): Show |
chr5 | 56810549 | 56901152 |
| a0003c0002t0011 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7028): Show |
chr5 | 56810549 | 56901152 |
| a0003c0002t0014 | 0/0 | 7033 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7028): Show |
chr5 | 56810549 | 56901152 |
| a0003c0009t0001 | 0/0 | 7033 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7028): Show |
chr5 | 56810549 | 56901152 |
| a0003c0009t0004 | 0/0 | 7034 | 2 | 1 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7029): Show |
chr5 | 56810549 | 56901152 |
| a0004c0010t0003 | 0/0 | 7035 | 4 | 0 | 3 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7030): Show |
chr5 | 56810549 | 56901152 |
| a0005c0012t0008 | 0/0 | 7035 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7030): Show |
chr5 | 56810549 | 56901152 |
| a0005c0012t0010 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7028): Show |
chr5 | 56810549 | 56901152 |
| a0005c0015t0008 | 0/0 | 7035 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7030): Show |
chr5 | 56810549 | 56901152 |
| a0006c0013t0002 | 0/0 | 7034 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7029): Show |
chr5 | 56810549 | 56901152 |
| a0006c0013t0018 | 0/1 | 7032 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7027): Show |
chr5 | 56810549 | 56901152 |
| a0007c0020t0012 | 0/0 | 7036 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7031): Show |
chr5 | 56810549 | 56901152 |
| a0008c0017t0002 | 0/0 | 7034 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7029): Show |
chr5 | 56810549 | 56901152 |
| a0009c0016t0002 | 0/0 | 7034 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7029): Show |
chr5 | 56810549 | 56901152 |
| a0010c0014t0004 | 0/0 | 7037 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7032): Show |
chr5 | 56810549 | 56901152 |
| a0011c0018t0004 | 0/0 | 7037 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7032): Show |
chr5 | 56810549 | 56901152 |
| a0012c0019t0004 | 0/0 | 7037 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | GAGCG others(7032): Show |
chr5 | 56810549 | 56901152 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0005 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0012 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0008g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0008g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0008g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0008g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0008g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0008g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0008g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0009g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0009g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0009g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0009g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0009g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0009g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0009g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0009g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0010g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0010g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0010g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0011g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0015g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0001t0017g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0007g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0007g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0005t0013g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0003g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0004g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0006t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0008t0007g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0008t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0008t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0008t0011g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0011t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0011t0007g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0011t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0001c0011t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0005g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0005g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0005g0008 | 1/0 | 3 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0006g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0006g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0006g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0012g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0012g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0016g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0019g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0003t0020g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0004g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0004g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0004g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0004t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0007t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0007t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0007t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0007t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0007t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0007t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0002c0007t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0003g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0006g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0011g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0002t0014g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0009t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0009t0004g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0003c0009t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0004c0010t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0004c0010t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0004c0010t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0004c0010t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0005c0012t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0005c0012t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0005c0012t0010g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0005c0015t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0006c0013t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0006c0013t0018g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0007c0020t0012g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0008c0017t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0009c0016t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0010c0014t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0011c0018t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| a0012c0019t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0002 | t0001 | g0190 | EUR | GBR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0256 | EUR | FIN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00280 | hp2 | a0002 | c0004 | t0001 | g0045 | EUR | FIN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00423 | hp1 | a0002 | c0003 | t0006 | g0018 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00423 | hp2 | a0001 | c0006 | t0004 | g0011 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00438 | hp1 | a0001 | c0001 | t0008 | g0267 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00438 | hp2 | a0003 | c0002 | t0001 | g0010 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00544 | hp1 | a0002 | c0003 | t0005 | g0004 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00544 | hp2 | a0002 | c0004 | t0003 | g0076 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00558 | hp1 | a0003 | c0002 | t0001 | g0013 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00558 | hp2 | a0002 | c0003 | t0019 | g0002 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00597 | hp1 | a0002 | c0003 | t0005 | g0004 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00597 | hp2 | a0003 | c0002 | t0004 | g0167 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00609 | hp2 | a0002 | c0003 | t0006 | g0113 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00621 | hp1 | a0003 | c0002 | t0001 | g0151 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00621 | hp2 | a0002 | c0004 | t0001 | g0105 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00639 | hp1 | a0003 | c0002 | t0001 | g0159 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00642 | hp1 | a0002 | c0003 | t0001 | g0060 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00642 | hp2 | a0006 | c0013 | t0002 | g0294 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00673 | hp1 | a0003 | c0002 | t0001 | g0149 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00673 | hp2 | a0001 | c0005 | t0001 | g0227 | EAS | CHS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00738 | hp1 | a0002 | c0004 | t0001 | g0077 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG00741 | hp2 | a0002 | c0003 | t0006 | g0117 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01069 | hp1 | a0002 | c0004 | t0001 | g0074 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01069 | hp2 | a0003 | c0002 | t0003 | g0020 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01071 | hp1 | a0003 | c0002 | t0003 | g0020 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01081 | hp1 | a0002 | c0007 | t0001 | g0054 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01081 | hp2 | a0001 | c0011 | t0007 | g0199 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01109 | hp2 | a0003 | c0002 | t0001 | g0183 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01167 | hp2 | a0002 | c0003 | t0001 | g0055 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01168 | hp1 | a0002 | c0004 | t0001 | g0084 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01168 | hp2 | a0003 | c0002 | t0001 | g0189 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01169 | hp1 | a0002 | c0004 | t0001 | g0068 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01192 | hp1 | a0003 | c0002 | t0001 | g0191 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01243 | hp2 | a0003 | c0009 | t0004 | g0318 | AMR | PUR | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01255 | hp1 | a0003 | c0002 | t0001 | g0010 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01256 | hp1 | a0002 | c0004 | t0001 | g0142 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01261 | hp1 | a0001 | c0006 | t0001 | g0237 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01261 | hp2 | a0002 | c0003 | t0006 | g0056 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01346 | hp1 | a0002 | c0003 | t0001 | g0062 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01361 | hp1 | a0002 | c0007 | t0001 | g0096 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01361 | hp2 | a0001 | c0006 | t0003 | g0241 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01433 | hp1 | a0001 | c0006 | t0003 | g0243 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01433 | hp2 | a0002 | c0007 | t0001 | g0016 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01496 | hp1 | a0002 | c0003 | t0004 | g0061 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01496 | hp2 | a0003 | c0002 | t0001 | g0003 | AMR | CLM | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01516 | hp1 | a0001 | c0006 | t0003 | g0024 | EUR | IBS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0299 | EUR | IBS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01517 | hp1 | a0001 | c0006 | t0003 | g0024 | EUR | IBS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0291 | EUR | IBS | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01884 | hp1 | a0002 | c0003 | t0001 | g0139 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01884 | hp2 | a0001 | c0005 | t0007 | g0317 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0306 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01891 | hp2 | a0003 | c0002 | t0003 | g0039 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01928 | hp1 | a0004 | c0010 | t0003 | g0249 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01928 | hp2 | a0002 | c0003 | t0005 | g0132 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01934 | hp2 | a0002 | c0007 | t0001 | g0002 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01943 | hp1 | a0004 | c0010 | t0003 | g0248 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01943 | hp2 | a0002 | c0004 | t0004 | g0015 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0002 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01981 | hp2 | a0002 | c0004 | t0004 | g0079 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01993 | hp1 | a0002 | c0007 | t0001 | g0095 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02015 | hp1 | a0002 | c0004 | t0003 | g0119 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02015 | hp2 | a0007 | c0020 | t0012 | g0128 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02040 | hp1 | a0002 | c0003 | t0001 | g0115 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02040 | hp2 | a0002 | c0003 | t0001 | g0097 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02055 | hp2 | a0002 | c0003 | t0016 | g0098 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02056 | hp1 | a0002 | c0003 | t0005 | g0004 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02056 | hp2 | a0001 | c0006 | t0004 | g0245 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02071 | hp1 | a0002 | c0004 | t0004 | g0001 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02071 | hp2 | a0002 | c0003 | t0004 | g0112 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02080 | hp1 | a0001 | c0005 | t0003 | g0222 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02080 | hp2 | a0002 | c0004 | t0004 | g0073 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02083 | hp1 | a0003 | c0002 | t0001 | g0155 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02083 | hp2 | a0002 | c0004 | t0004 | g0072 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02129 | hp1 | a0001 | c0001 | t0008 | g0194 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02129 | hp2 | a0002 | c0004 | t0004 | g0001 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02132 | hp1 | a0003 | c0002 | t0001 | g0160 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02132 | hp2 | a0002 | c0003 | t0006 | g0114 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02135 | hp1 | a0003 | c0002 | t0004 | g0157 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02135 | hp2 | a0001 | c0006 | t0004 | g0011 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02145 | hp1 | a0005 | c0012 | t0010 | g0058 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0327 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02148 | hp1 | a0002 | c0004 | t0004 | g0006 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02148 | hp2 | a0002 | c0003 | t0005 | g0131 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02155 | hp1 | a0001 | c0006 | t0004 | g0011 | EAS | CDX | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02155 | hp2 | a0003 | c0002 | t0001 | g0148 | EAS | CDX | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02273 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02293 | hp1 | a0002 | c0007 | t0001 | g0016 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02293 | hp2 | a0004 | c0010 | t0003 | g0251 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02300 | hp1 | a0002 | c0007 | t0001 | g0087 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02300 | hp2 | a0001 | c0001 | t0010 | g0027 | AMR | PEL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02451 | hp1 | a0001 | c0005 | t0007 | g0316 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02523 | hp1 | a0003 | c0002 | t0004 | g0003 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02523 | hp2 | a0002 | c0003 | t0005 | g0004 | EAS | KHV | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0030 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02572 | hp2 | a0002 | c0004 | t0001 | g0006 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02615 | hp1 | a0002 | c0004 | t0001 | g0001 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02615 | hp2 | a0003 | c0002 | t0006 | g0042 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02622 | hp1 | a0002 | c0004 | t0001 | g0082 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02622 | hp2 | a0003 | c0002 | t0007 | g0037 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02630 | hp1 | a0003 | c0002 | t0006 | g0014 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02630 | hp2 | a0005 | c0012 | t0008 | g0059 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02683 | hp1 | a0002 | c0003 | t0001 | g0085 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02698 | hp2 | a0001 | c0005 | t0004 | g0231 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02717 | hp1 | a0001 | c0011 | t0007 | g0200 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02717 | hp2 | a0003 | c0002 | t0006 | g0043 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02723 | hp1 | a0001 | c0005 | t0007 | g0315 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02723 | hp2 | a0001 | c0011 | t0007 | g0198 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02735 | hp2 | a0002 | c0004 | t0004 | g0048 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02738 | hp1 | a0003 | c0002 | t0001 | g0182 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02738 | hp2 | a0008 | c0017 | t0002 | g0301 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02809 | hp1 | a0001 | c0008 | t0007 | g0202 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02818 | hp1 | a0001 | c0001 | t0008 | g0209 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0292 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0325 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02895 | hp2 | a0002 | c0003 | t0001 | g0049 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0140 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02896 | hp2 | a0003 | c0002 | t0004 | g0038 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0019 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02965 | hp1 | a0002 | c0003 | t0001 | g0091 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0323 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0053 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0326 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0122 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02976 | hp2 | a0003 | c0009 | t0004 | g0319 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03017 | hp1 | a0002 | c0003 | t0001 | g0090 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03041 | hp1 | a0003 | c0002 | t0006 | g0014 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03041 | hp2 | a0001 | c0005 | t0007 | g0314 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03098 | hp1 | a0003 | c0002 | t0001 | g0032 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03098 | hp2 | a0005 | c0015 | t0008 | g0208 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03139 | hp1 | a0003 | c0009 | t0001 | g0029 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03139 | hp2 | a0003 | c0002 | t0006 | g0040 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03195 | hp1 | a0003 | c0002 | t0001 | g0031 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03195 | hp2 | a0003 | c0009 | t0001 | g0029 | AFR | ESN | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03209 | hp1 | a0001 | c0011 | t0007 | g0201 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03209 | hp2 | a0002 | c0003 | t0001 | g0019 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03225 | hp1 | a0001 | c0008 | t0007 | g0022 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0307 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03239 | hp1 | a0003 | c0002 | t0014 | g0003 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03239 | hp2 | a0001 | c0005 | t0003 | g0225 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0030 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03486 | hp1 | a0003 | c0002 | t0006 | g0036 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0328 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03491 | hp2 | a0002 | c0004 | t0001 | g0015 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03492 | hp2 | a0002 | c0004 | t0004 | g0075 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03540 | hp1 | a0001 | c0008 | t0007 | g0022 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0321 | AFR | GWD | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03579 | hp1 | a0002 | c0003 | t0001 | g0089 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0320 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03654 | hp1 | a0003 | c0002 | t0001 | g0193 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03669 | hp1 | a0003 | c0002 | t0001 | g0146 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03669 | hp2 | a0002 | c0003 | t0012 | g0124 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03688 | hp1 | a0003 | c0002 | t0001 | g0172 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03688 | hp2 | a0009 | c0016 | t0002 | g0280 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03704 | hp1 | a0002 | c0004 | t0004 | g0103 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03704 | hp2 | a0001 | c0006 | t0003 | g0252 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0290 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03710 | hp2 | a0002 | c0003 | t0001 | g0093 | SAS | PJL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0262 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03831 | hp2 | a0001 | c0005 | t0003 | g0229 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03834 | hp1 | a0002 | c0004 | t0004 | g0120 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03834 | hp2 | a0003 | c0002 | t0001 | g0156 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03927 | hp1 | a0003 | c0002 | t0001 | g0147 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03927 | hp2 | a0001 | c0001 | t0017 | g0305 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03942 | hp1 | a0003 | c0002 | t0004 | g0186 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03942 | hp2 | a0010 | c0014 | t0004 | g0083 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG04115 | hp1 | a0002 | c0004 | t0001 | g0080 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG04115 | hp2 | a0003 | c0002 | t0001 | g0180 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0308 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG04184 | hp2 | a0002 | c0003 | t0001 | g0108 | SAS | BEB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG04199 | hp2 | a0003 | c0002 | t0001 | g0188 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG04204 | hp1 | a0003 | c0002 | t0001 | g0179 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG04204 | hp2 | a0003 | c0002 | t0001 | g0145 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG04228 | hp1 | a0003 | c0002 | t0001 | g0181 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0282 | SAS | STU | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0047 | AFR | YRI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18522 | hp2 | a0003 | c0002 | t0006 | g0041 | AFR | YRI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18612 | hp1 | a0003 | c0002 | t0004 | g0152 | EAS | CHB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18612 | hp2 | a0002 | c0003 | t0001 | g0017 | EAS | CHB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18942 | hp1 | a0002 | c0003 | t0020 | g0123 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18942 | hp2 | a0003 | c0002 | t0001 | g0165 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18945 | hp1 | a0003 | c0002 | t0001 | g0021 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18945 | hp2 | a0001 | c0005 | t0003 | g0221 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18946 | hp1 | a0003 | c0002 | t0001 | g0168 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18946 | hp2 | a0002 | c0004 | t0001 | g0051 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18947 | hp1 | a0002 | c0004 | t0001 | g0104 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18947 | hp2 | a0003 | c0002 | t0004 | g0010 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18948 | hp1 | a0001 | c0005 | t0003 | g0216 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18948 | hp2 | a0002 | c0004 | t0004 | g0081 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18953 | hp2 | a0002 | c0003 | t0005 | g0008 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18956 | hp1 | a0001 | c0006 | t0003 | g0247 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18956 | hp2 | a0003 | c0002 | t0001 | g0162 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18957 | hp1 | a0003 | c0002 | t0001 | g0175 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18957 | hp2 | a0002 | c0004 | t0001 | g0069 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18959 | hp1 | a0002 | c0004 | t0001 | g0065 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18959 | hp2 | a0001 | c0005 | t0003 | g0220 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18960 | hp1 | a0001 | c0001 | t0015 | g0265 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18960 | hp2 | a0001 | c0005 | t0003 | g0224 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18961 | hp1 | a0002 | c0003 | t0005 | g0099 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18961 | hp2 | a0002 | c0003 | t0001 | g0126 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18962 | hp1 | a0001 | c0001 | t0010 | g0268 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18962 | hp2 | a0002 | c0003 | t0005 | g0007 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18963 | hp1 | a0003 | c0002 | t0001 | g0185 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18964 | hp1 | a0003 | c0002 | t0001 | g0033 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18964 | hp2 | a0002 | c0004 | t0001 | g0067 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18965 | hp1 | a0002 | c0003 | t0001 | g0101 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18965 | hp2 | a0003 | c0002 | t0001 | g0034 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18966 | hp1 | a0002 | c0004 | t0001 | g0143 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18966 | hp2 | a0002 | c0003 | t0001 | g0107 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18968 | hp1 | a0001 | c0005 | t0003 | g0228 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18968 | hp2 | a0002 | c0003 | t0001 | g0109 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18969 | hp1 | a0001 | c0006 | t0003 | g0236 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18969 | hp2 | a0002 | c0004 | t0001 | g0138 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18971 | hp1 | a0002 | c0003 | t0005 | g0008 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18972 | hp1 | a0001 | c0006 | t0003 | g0233 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18972 | hp2 | a0002 | c0003 | t0006 | g0017 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18973 | hp1 | a0003 | c0002 | t0001 | g0144 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18973 | hp2 | a0002 | c0004 | t0004 | g0001 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18974 | hp1 | a0003 | c0002 | t0001 | g0013 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18974 | hp2 | a0002 | c0003 | t0001 | g0050 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18975 | hp1 | a0002 | c0004 | t0004 | g0001 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18975 | hp2 | a0003 | c0002 | t0001 | g0170 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18977 | hp1 | a0003 | c0002 | t0001 | g0174 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18977 | hp2 | a0002 | c0004 | t0001 | g0078 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18979 | hp1 | a0002 | c0003 | t0005 | g0133 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18979 | hp2 | a0003 | c0002 | t0001 | g0154 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18981 | hp2 | a0001 | c0005 | t0003 | g0023 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18982 | hp1 | a0003 | c0002 | t0001 | g0161 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18982 | hp2 | a0001 | c0005 | t0003 | g0218 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18983 | hp1 | a0002 | c0003 | t0005 | g0129 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18983 | hp2 | a0003 | c0002 | t0001 | g0003 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18985 | hp1 | a0001 | c0005 | t0003 | g0223 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18985 | hp2 | a0002 | c0003 | t0001 | g0116 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18986 | hp1 | a0003 | c0002 | t0001 | g0177 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18986 | hp2 | a0002 | c0003 | t0001 | g0066 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18987 | hp1 | a0002 | c0003 | t0005 | g0127 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18989 | hp1 | a0003 | c0002 | t0001 | g0166 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18989 | hp2 | a0002 | c0004 | t0001 | g0063 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18990 | hp1 | a0002 | c0003 | t0001 | g0135 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18990 | hp2 | a0002 | c0004 | t0005 | g0071 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18992 | hp1 | a0003 | c0002 | t0001 | g0163 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18992 | hp2 | a0002 | c0004 | t0004 | g0001 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18993 | hp1 | a0003 | c0002 | t0004 | g0187 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18993 | hp2 | a0001 | c0001 | t0008 | g0197 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18995 | hp2 | a0002 | c0003 | t0005 | g0004 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18998 | hp1 | a0003 | c0002 | t0001 | g0003 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18998 | hp2 | a0001 | c0006 | t0003 | g0242 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18999 | hp1 | a0003 | c0002 | t0001 | g0158 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18999 | hp2 | a0002 | c0004 | t0004 | g0001 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19001 | hp1 | a0001 | c0005 | t0003 | g0230 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19001 | hp2 | a0002 | c0003 | t0006 | g0018 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19002 | hp1 | a0004 | c0010 | t0003 | g0250 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19002 | hp2 | a0011 | c0018 | t0004 | g0064 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19003 | hp1 | a0001 | c0005 | t0003 | g0226 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19003 | hp2 | a0003 | c0002 | t0001 | g0150 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19005 | hp1 | a0003 | c0002 | t0004 | g0171 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19005 | hp2 | a0001 | c0001 | t0008 | g0271 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19006 | hp1 | a0003 | c0002 | t0001 | g0176 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19006 | hp2 | a0001 | c0006 | t0003 | g0235 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19007 | hp1 | a0001 | c0005 | t0003 | g0023 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19007 | hp2 | a0002 | c0003 | t0005 | g0137 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19009 | hp1 | a0003 | c0002 | t0001 | g0021 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19009 | hp2 | a0001 | c0005 | t0013 | g0232 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19011 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19011 | hp2 | a0003 | c0002 | t0001 | g0184 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19012 | hp1 | a0002 | c0003 | t0001 | g0118 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19043 | hp1 | a0001 | c0008 | t0007 | g0204 | AFR | LWK | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19043 | hp2 | a0001 | c0005 | t0007 | g0313 | AFR | LWK | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19054 | hp1 | a0001 | c0006 | t0003 | g0246 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19054 | hp2 | a0001 | c0001 | t0008 | g0195 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19056 | hp1 | a0003 | c0002 | t0001 | g0153 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19056 | hp2 | a0002 | c0003 | t0005 | g0007 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19057 | hp1 | a0012 | c0019 | t0004 | g0070 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19057 | hp2 | a0002 | c0003 | t0005 | g0007 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19058 | hp1 | a0002 | c0003 | t0001 | g0121 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19060 | hp1 | a0003 | c0002 | t0001 | g0003 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19060 | hp2 | a0001 | c0005 | t0003 | g0214 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19063 | hp1 | a0001 | c0006 | t0003 | g0238 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19063 | hp2 | a0002 | c0004 | t0001 | g0106 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19068 | hp1 | a0002 | c0003 | t0005 | g0134 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19068 | hp2 | a0003 | c0002 | t0001 | g0164 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19076 | hp1 | a0001 | c0005 | t0003 | g0215 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19076 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19077 | hp1 | a0003 | c0002 | t0001 | g0173 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19077 | hp2 | a0002 | c0003 | t0001 | g0052 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19078 | hp2 | a0002 | c0004 | t0004 | g0110 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19079 | hp2 | a0002 | c0003 | t0001 | g0100 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19080 | hp1 | a0001 | c0005 | t0003 | g0217 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19080 | hp2 | a0003 | c0002 | t0001 | g0169 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19081 | hp1 | a0002 | c0003 | t0006 | g0111 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19084 | hp1 | a0002 | c0003 | t0001 | g0125 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19084 | hp2 | a0002 | c0003 | t0012 | g0086 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19085 | hp2 | a0002 | c0004 | t0001 | g0046 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19088 | hp1 | a0002 | c0004 | t0004 | g0006 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19088 | hp2 | a0001 | c0005 | t0003 | g0219 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19090 | hp1 | a0002 | c0003 | t0005 | g0130 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19090 | hp2 | a0001 | c0001 | t0008 | g0196 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19091 | hp1 | a0002 | c0003 | t0005 | g0102 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19091 | hp2 | a0002 | c0003 | t0001 | g0136 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19240 | hp1 | a0003 | c0002 | t0011 | g0207 | AFR | YRI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA19240 | hp2 | a0003 | c0002 | t0006 | g0035 | AFR | YRI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0009 | AFR | ASW | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA20129 | hp2 | a0002 | c0007 | t0001 | g0094 | AFR | ASW | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0289 | EUR | TSI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0206 | EUR | TSI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA20805 | hp1 | a0002 | c0003 | t0001 | g0141 | EUR | TSI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA20805 | hp2 | a0003 | c0002 | t0001 | g0192 | EUR | TSI | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA20905 | hp1 | a0002 | c0004 | t0004 | g0001 | SAS | GIH | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | GIH | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02109 | hp1 | a0001 | c0006 | t0003 | g0244 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02109 | hp2 | a0005 | c0012 | t0008 | g0057 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02486 | hp1 | a0001 | c0006 | t0003 | g0239 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0092 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG02559 | hp2 | a0003 | c0002 | t0006 | g0044 | AFR | ACB | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03471 | hp1 | a0001 | c0001 | t0009 | g0322 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG03471 | hp2 | a0001 | c0008 | t0011 | g0203 | AFR | MSL | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG06807 | hp1 | a0001 | c0006 | t0003 | g0240 | AFR | USA | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | USA | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18955 | hp1 | a0003 | c0002 | t0001 | g0178 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA18955 | hp2 | a0001 | c0006 | t0003 | g0234 | EAS | JPT | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA20300 | hp1 | a0001 | c0001 | t0009 | g0324 | AFR | USA | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | USA | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | LWK | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| NA21309 | hp2 | a0002 | c0003 | t0001 | g0088 | AFR | LWK | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| homoSapiens | chm13v2 | a0006 | c0013 | t0018 | g0257 | REF | REF | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0005 | g0008 | REF | REF | MAP3K1_chr5_56810549_56901152 | MAP3K1 | chr5 | 56810549 | 56901152 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:56815806 | T | C | 1 | a0004 | 4 | HG01928.hp1 HG01943.hp1 HG02293.hp2 others(1): Show |
missense_variant | MODERATE | c.233T>C | p.Leu78Pro | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 258/7036 | 233/4539 | 78/1512 | chr5 | 56815806 | |||
| chr5:56815877 | G | A | 1 | a0010 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.304G>A | p.Gly102Arg | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 329/7036 | 304/4539 | 102/1512 | chr5 | 56815877 | |||
| chr5:56815967 | G | C | 1 | a0010 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.394G>C | p.Asp132His | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 419/7036 | 394/4539 | 132/1512 | chr5 | 56815967 | |||
| chr5:56859845 | A | G | 1 | a0005 | 4 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
missense_variant | MODERATE | c.764A>G | p.Asn255Ser | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/20 | 789/7036 | 764/4539 | 255/1512 | chr5 | 56859845 | |||
| chr5:56864836 | C | T | 1 | a0008 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.937C>T | p.Arg313Trp | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 4/20 | 962/7036 | 937/4539 | 313/1512 | chr5 | 56864836 | |||
| chr5:56881185 | T | C | 1 | a0007 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.2282T>C | p.Ile761Thr | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 13/20 | 2307/7036 | 2282/4539 | 761/1512 | chr5 | 56881185 | |||
| chr5:56881616 | G | A | 6 | a0001 a0004 a0005 others(3): Show |
160 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(157): Show |
missense_variant | MODERATE | c.2416G>A | p.Asp806Asn | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 2441/7036 | 2416/4539 | 806/1512 | chr5 | 56881616 | |||
| chr5:56881647 | C | G | 1 | a0009 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2447C>G | p.Ser816Cys | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 2472/7036 | 2447/4539 | 816/1512 | chr5 | 56881647 | |||
| chr5:56881916 | G | A | 7 | a0001 a0003 a0004 others(4): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
missense_variant | MODERATE | c.2716G>A | p.Val906Ile | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 2741/7036 | 2716/4539 | 906/1512 | chr5 | 56881916 | |||
| chr5:56882016 | C | G | 1 | a0006 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.2816C>G | p.Ser939Cys | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 2841/7036 | 2816/4539 | 939/1512 | chr5 | 56882016 | |||
| chr5:56882021 | TCAA | T | 7 | a0001 a0003 a0004 others(4): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
conservative_inframe_deletion | MODERATE | c.2845_2847delACA | p.Thr949del | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 2870/7036 | 2845/4539 | 949/1512 | INFO_REALIGN_3_PRIME | chr5 | 56882021 | ||
| chr5:56882315 | T | C | 1 | a0011 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.3115T>C | p.Ser1039Pro | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 3140/7036 | 3115/4539 | 1039/1512 | chr5 | 56882315 | |||
| chr5:56883573 | G | A | 1 | a0012 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.3713G>A | p.Arg1238Lys | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/20 | 3738/7036 | 3713/4539 | 1238/1512 | chr5 | 56883573 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:56815618 | G | A | 1 | a0003c0009 | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
synonymous_variant | LOW | c.45G>A | p.Pro15Pro | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 70/7036 | 45/4539 | 15/1512 | chr5 | 56815618 | |||
| chr5:56815654 | C | T | 1 | a0002c0007 | 8 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(5): Show |
synonymous_variant | LOW | c.81C>T | p.Gly27Gly | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 106/7036 | 81/4539 | 27/1512 | chr5 | 56815654 | |||
| chr5:56815738 | G | A | 1 | a0003c0009 | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
synonymous_variant | LOW | c.165G>A | p.Ala55Ala | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 190/7036 | 165/4539 | 55/1512 | chr5 | 56815738 | |||
| chr5:56815807 | C | T | 1 | a0004c0010 | 4 | HG01928.hp1 HG01943.hp1 HG02293.hp2 others(1): Show |
synonymous_variant | LOW | c.234C>T | p.Leu78Leu | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 259/7036 | 234/4539 | 78/1512 | chr5 | 56815807 | |||
| chr5:56815924 | G | C | 11 | a0001c0001 a0001c0005 a0001c0006 others(8): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
synonymous_variant | LOW | c.351G>C | p.Ala117Ala | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/20 | 376/7036 | 351/4539 | 117/1512 | chr5 | 56815924 | |||
| chr5:56859801 | G | A | 2 | a0005c0012 a0005c0015 |
4 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
synonymous_variant | LOW | c.720G>A | p.Ala240Ala | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/20 | 745/7036 | 720/4539 | 240/1512 | chr5 | 56859801 | |||
| chr5:56865960 | G | A | 17 | a0001c0001 a0001c0005 a0001c0006 others(14): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
synonymous_variant | LOW | c.1284G>A | p.Thr428Thr | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/20 | 1309/7036 | 1284/4539 | 428/1512 | chr5 | 56865960 | |||
| chr5:56872885 | C | T | 2 | a0001c0006 a0004c0010 |
25 | HG00423.hp2 HG01261.hp1 HG01361.hp2 others(22): Show |
synonymous_variant | LOW | c.1566C>T | p.Thr522Thr | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/20 | 1591/7036 | 1566/4539 | 522/1512 | chr5 | 56872885 | |||
| chr5:56872963 | A | G | 1 | a0003c0009 | 4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
synonymous_variant | LOW | c.1644A>G | p.Gln548Gln | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/20 | 1669/7036 | 1644/4539 | 548/1512 | chr5 | 56872963 | |||
| chr5:56875262 | G | A | 2 | a0001c0008 a0001c0011 |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
synonymous_variant | LOW | c.1917G>A | p.Leu639Leu | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/20 | 1942/7036 | 1917/4539 | 639/1512 | chr5 | 56875262 | |||
| chr5:56882284 | A | G | 5 | a0001c0005 a0001c0006 a0001c0008 others(2): Show |
60 | HG00423.hp2 HG00673.hp2 HG01081.hp2 others(57): Show |
synonymous_variant | LOW | c.3084A>G | p.Gln1028Gln | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 3109/7036 | 3084/4539 | 1028/1512 | chr5 | 56882284 | |||
| chr5:56882287 | C | T | 1 | a0001c0011 | 4 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
synonymous_variant | LOW | c.3087C>T | p.Phe1029Phe | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 3112/7036 | 3087/4539 | 1029/1512 | chr5 | 56882287 | |||
| chr5:56882390 | A | C | 13 | a0001c0001 a0001c0005 a0001c0006 others(10): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
synonymous_variant | LOW | c.3190A>C | p.Arg1064Arg | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 3215/7036 | 3190/4539 | 1064/1512 | chr5 | 56882390 | |||
| chr5:56882839 | A | G | 1 | a0005c0015 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.3639A>G | p.Gly1213Gly | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/20 | 3664/7036 | 3639/4539 | 1213/1512 | chr5 | 56882839 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:56894072 | G | T | 1 | a0002c0003t0020 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*392G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 392 | chr5 | 56894072 | ||||||
| chr5:56894081 | T | C | 1 | a0001c0005t0013 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*401T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 401 | chr5 | 56894081 | ||||||
| chr5:56894704 | G | A | 47 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(44): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
3_prime_UTR_variant | MODIFIER | c.*1024G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1024 | chr5 | 56894704 | ||||||
| chr5:56895007 | A | G | 1 | a0002c0003t0019 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1327A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1327 | chr5 | 56895007 | ||||||
| chr5:56895063 | G | C | 1 | a0003c0002t0014 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1383G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1383 | chr5 | 56895063 | ||||||
| chr5:56895159 | A | G | 21 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(18): Show |
117 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1479A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1479 | chr5 | 56895159 | ||||||
| chr5:56895283 | G | T | 2 | a0002c0003t0012 a0007c0020t0012 |
3 | HG02015.hp2 HG03669.hp2 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1603G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1603 | chr5 | 56895283 | ||||||
| chr5:56895364 | TTG | T | 12 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(9): Show |
90 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1686_*1687delGT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1686 | INFO_REALIGN_3_PRIME | chr5 | 56895364 | |||||
| chr5:56895366 | G | GT | 4 | a0001c0011t0007 a0002c0003t0005 a0002c0004t0001 others(1): Show |
7 | HG01081.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1701dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1702 | INFO_REALIGN_3_PRIME | chr5 | 56895366 | |||||
| chr5:56895366 | G | GTT | 3 | a0001c0005t0007 a0003c0009t0001 a0003c0009t0004 |
8 | HG01243.hp2 HG01884.hp2 HG02451.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1700_*1701dupTT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1702 | INFO_REALIGN_3_PRIME | chr5 | 56895366 | |||||
| chr5:56895366 | GT | G | 3 | a0002c0003t0001 a0002c0003t0006 a0003c0002t0001 |
6 | HG00741.hp2 HG01167.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1701delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1701 | INFO_REALIGN_3_PRIME | chr5 | 56895366 | |||||
| chr5:56895366 | GTT | G | 5 | a0001c0005t0003 a0003c0002t0001 a0003c0002t0003 others(2): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1700_*1701delTT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1700 | INFO_REALIGN_3_PRIME | chr5 | 56895366 | |||||
| chr5:56895373 | T | A | 12 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(9): Show |
90 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1693T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1693 | chr5 | 56895373 | ||||||
| chr5:56895559 | T | G | 1 | a0001c0001t0015 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1879T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1879 | chr5 | 56895559 | ||||||
| chr5:56895634 | T | C | 1 | a0002c0003t0016 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1954T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 1954 | chr5 | 56895634 | ||||||
| chr5:56895976 | C | CA | 17 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0015 others(14): Show |
123 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2314dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 2315 | INFO_REALIGN_3_PRIME | chr5 | 56895976 | |||||
| chr5:56895976 | C | CAA | 14 | a0001c0001t0007 a0001c0001t0008 a0001c0005t0003 others(11): Show |
71 | HG00438.hp1 HG00544.hp2 HG01069.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2313_*2314dupAA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 2315 | INFO_REALIGN_3_PRIME | chr5 | 56895976 | |||||
| chr5:56895976 | CA | C | 2 | a0002c0003t0006 a0003c0002t0006 |
17 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2314delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 2314 | INFO_REALIGN_3_PRIME | chr5 | 56895976 | |||||
| chr5:56896108 | T | C | 1 | a0001c0001t0017 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2428T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 20/20 | 2428 | chr5 | 56896108 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:56816100 | C | T | 147 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(144): Show |
162 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.482+45C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816100 | |||||||
| chr5:56816118 | C | T | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.482+63C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816118 | |||||||
| chr5:56816171 | G | A | 4 | a0001c0001t0008g0194 a0001c0001t0008g0195 a0001c0001t0008g0196 others(1): Show |
4 | HG02129.hp1 NA18993.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+116G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816171 | |||||||
| chr5:56816270 | G | A | 2 | a0003c0002t0001g0031 a0003c0002t0001g0032 |
2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.482+215G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816270 | |||||||
| chr5:56816462 | G | A | 4 | a0001c0011t0007g0198 a0001c0011t0007g0199 a0001c0011t0007g0200 others(1): Show |
4 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+407G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816462 | |||||||
| chr5:56816554 | G | T | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+499G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816554 | |||||||
| chr5:56816717 | G | C | 1 | a0001c0011t0007g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.482+662G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816717 | |||||||
| chr5:56816718 | T | A | 1 | a0001c0011t0007g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.482+663T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816718 | |||||||
| chr5:56816762 | G | A | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+707G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816762 | |||||||
| chr5:56816767 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.482+712G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816767 | |||||||
| chr5:56816791 | A | C | 1 | a0003c0002t0001g0193 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.482+736A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816791 | |||||||
| chr5:56816824 | G | A | 3 | a0003c0002t0001g0013 a0003c0002t0001g0033 a0003c0002t0001g0034 |
4 | HG00558.hp1 NA18964.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+769G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816824 | |||||||
| chr5:56816871 | C | T | 59 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(56): Show |
65 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.482+816C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816871 | |||||||
| chr5:56816907 | C | T | 1 | a0002c0004t0001g0143 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.482+852C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56816907 | |||||||
| chr5:56817033 | G | A | 13 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(10): Show |
14 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.482+978G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817033 | |||||||
| chr5:56817087 | C | T | 3 | a0001c0008t0007g0022 a0001c0008t0007g0204 a0001c0008t0011g0203 |
4 | HG03225.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+1032C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817087 | |||||||
| chr5:56817211 | CTTGT | C | 7 | a0001c0005t0007g0313 a0001c0005t0007g0314 a0001c0005t0007g0315 others(4): Show |
7 | HG01192.hp1 HG01884.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+1167_482+1170d others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56817211 | ||||||
| chr5:56817262 | C | A | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+1207C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817262 | |||||||
| chr5:56817615 | C | T | 14 | a0003c0002t0001g0179 a0003c0002t0001g0180 a0003c0002t0001g0181 others(11): Show |
14 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.482+1560C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817615 | |||||||
| chr5:56817683 | T | G | 2 | a0003c0002t0001g0179 a0003c0002t0001g0180 |
2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.482+1628T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817683 | |||||||
| chr5:56817736 | T | A | 1 | a0001c0001t0002g0206 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.482+1681T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817736 | |||||||
| chr5:56817737 | G | T | 6 | a0003c0002t0006g0014 a0003c0002t0006g0040 a0003c0002t0006g0041 others(3): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+1682G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817737 | |||||||
| chr5:56817962 | G | C | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+1907G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56817962 | |||||||
| chr5:56818023 | G | T | 72 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(69): Show |
80 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.482+1968G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818023 | |||||||
| chr5:56818176 | G | A | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+2121G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818176 | |||||||
| chr5:56818313 | C | A | 1 | a0002c0004t0001g0045 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.482+2258C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818313 | |||||||
| chr5:56818348 | G | T | 2 | a0002c0004t0001g0045 a0002c0004t0001g0142 |
2 | HG00280.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.482+2293G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818348 | |||||||
| chr5:56818435 | C | T | 1 | a0002c0003t0001g0141 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.482+2380C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818435 | |||||||
| chr5:56818594 | G | A | 1 | a0003c0002t0001g0144 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.482+2539G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818594 | |||||||
| chr5:56818699 | T | G | 83 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(80): Show |
91 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.482+2644T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818699 | |||||||
| chr5:56818717 | G | C | 1 | a0001c0005t0003g0214 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.482+2662G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818717 | |||||||
| chr5:56818734 | A | G | 1 | a0001c0001t0009g0030 | 2 | HG02572.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.482+2679A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818734 | |||||||
| chr5:56818756 | A | G | 13 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(10): Show |
14 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.482+2701A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818756 | |||||||
| chr5:56818761 | A | G | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+2706A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818761 | |||||||
| chr5:56818908 | C | T | 1 | a0001c0001t0002g0312 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.482+2853C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818908 | |||||||
| chr5:56818959 | A | G | 217 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(214): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.482+2904A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818959 | |||||||
| chr5:56818993 | T | C | 1 | a0002c0004t0001g0046 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.482+2938T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56818993 | |||||||
| chr5:56819023 | A | G | 9 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(6): Show |
10 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.482+2968A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819023 | |||||||
| chr5:56819041 | TC | T | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.482+2988delC | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56819041 | ||||||
| chr5:56819158 | G | A | 1 | a0002c0003t0001g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.482+3103G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819158 | |||||||
| chr5:56819209 | A | G | 217 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(214): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.482+3154A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819209 | |||||||
| chr5:56819243 | G | T | 2 | a0001c0001t0002g0310 a0001c0001t0002g0311 |
2 | NA18981.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.482+3188G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819243 | |||||||
| chr5:56819438 | CA | C | 216 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(213): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.482+3393delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56819438 | ||||||
| chr5:56819525 | A | G | 3 | a0003c0002t0003g0039 a0003c0002t0004g0038 a0003c0002t0007g0037 |
3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+3470A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819525 | |||||||
| chr5:56819635 | ATCT | A | 4 | a0002c0003t0001g0009 a0002c0003t0001g0019 a0002c0003t0001g0139 others(1): Show |
7 | HG01884.hp1 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.482+3585_482+3587d others(5): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56819635 | ||||||
| chr5:56819675 | T | A | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+3620T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819675 | |||||||
| chr5:56819707 | C | G | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+3652C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819707 | |||||||
| chr5:56819714 | C | G | 1 | a0001c0008t0007g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.482+3659C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819714 | |||||||
| chr5:56819829 | A | G | 13 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(10): Show |
14 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.482+3774A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819829 | |||||||
| chr5:56819952 | A | G | 1 | a0001c0006t0003g0252 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.482+3897A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56819952 | |||||||
| chr5:56820129 | T | C | 1 | a0001c0011t0007g0199 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.482+4074T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820129 | |||||||
| chr5:56820145 | A | G | 1 | a0001c0008t0007g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.482+4090A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820145 | |||||||
| chr5:56820258 | A | G | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.482+4203A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820258 | |||||||
| chr5:56820277 | A | G | 2 | a0003c0002t0006g0035 a0003c0002t0006g0036 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.482+4222A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820277 | |||||||
| chr5:56820319 | A | G | 1 | a0002c0004t0001g0138 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.482+4264A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820319 | |||||||
| chr5:56820384 | T | G | 20 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(17): Show |
21 | HG00673.hp2 HG02080.hp1 HG02698.hp2 others(18): Show |
intron_variant | MODIFIER | c.482+4329T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820384 | |||||||
| chr5:56820424 | A | G | 3 | a0003c0002t0003g0039 a0003c0002t0004g0038 a0003c0002t0007g0037 |
3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+4369A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820424 | |||||||
| chr5:56820580 | A | G | 1 | a0001c0011t0007g0199 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.482+4525A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820580 | |||||||
| chr5:56820706 | C | T | 3 | a0003c0002t0001g0176 a0003c0002t0001g0177 a0003c0002t0001g0178 |
3 | NA18955.hp1 NA18986.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.482+4651C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820706 | |||||||
| chr5:56820806 | T | C | 1 | a0002c0003t0001g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.482+4751T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820806 | |||||||
| chr5:56820918 | C | T | 1 | a0003c0002t0003g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.482+4863C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820918 | |||||||
| chr5:56820945 | C | A | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.482+4890C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56820945 | |||||||
| chr5:56821079 | G | A | 1 | a0001c0001t0002g0253 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.482+5024G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821079 | |||||||
| chr5:56821271 | A | C | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+5216A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821271 | |||||||
| chr5:56821281 | G | C | 319 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(316): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.482+5226G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821281 | |||||||
| chr5:56821327 | G | A | 1 | a0001c0001t0002g0254 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.482+5272G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821327 | |||||||
| chr5:56821490 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.482+5435G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821490 | |||||||
| chr5:56821510 | A | T | 1 | a0001c0001t0002g0309 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.482+5455A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821510 | |||||||
| chr5:56821542 | A | C | 1 | a0002c0003t0005g0137 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.482+5487A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821542 | |||||||
| chr5:56821808 | C | T | 1 | a0002c0003t0001g0122 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.482+5753C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821808 | |||||||
| chr5:56821895 | A | C | 1 | a0001c0005t0013g0232 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.482+5840A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821895 | |||||||
| chr5:56821991 | T | G | 3 | a0003c0002t0001g0145 a0003c0002t0001g0146 a0003c0002t0001g0147 |
3 | HG03669.hp1 HG03927.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.482+5936T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56821991 | |||||||
| chr5:56822013 | C | T | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+5958C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822013 | |||||||
| chr5:56822100 | A | G | 1 | a0002c0003t0001g0121 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.482+6045A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822100 | |||||||
| chr5:56822125 | A | G | 93 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(90): Show |
102 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.482+6070A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822125 | |||||||
| chr5:56822398 | A | G | 3 | a0002c0003t0001g0019 a0002c0003t0001g0139 a0002c0003t0001g0140 |
4 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+6343A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822398 | |||||||
| chr5:56822439 | G | A | 1 | a0002c0004t0004g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.482+6384G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822439 | |||||||
| chr5:56822509 | G | A | 1 | a0001c0001t0002g0256 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.482+6454G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822509 | |||||||
| chr5:56822906 | A | T | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.482+6851A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822906 | |||||||
| chr5:56822922 | G | T | 1 | a0001c0005t0004g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.482+6867G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56822922 | |||||||
| chr5:56823037 | A | G | 13 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(10): Show |
14 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.482+6982A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56823037 | |||||||
| chr5:56823048 | G | A | 83 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(80): Show |
91 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.482+6993G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56823048 | |||||||
| chr5:56823068 | C | T | 4 | a0004c0010t0003g0248 a0004c0010t0003g0249 a0004c0010t0003g0250 others(1): Show |
4 | HG01928.hp1 HG01943.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+7013C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56823068 | |||||||
| chr5:56823203 | G | A | 1 | a0003c0002t0001g0031 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.482+7148G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56823203 | |||||||
| chr5:56823266 | C | T | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+7211C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56823266 | |||||||
| chr5:56823363 | C | A | 83 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(80): Show |
91 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.482+7308C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56823363 | |||||||
| chr5:56823649 | A | G | 2 | a0001c0005t0007g0316 a0001c0005t0007g0317 |
2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.482+7594A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56823649 | |||||||
| chr5:56824045 | A | G | 1 | a0001c0001t0002g0253 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.482+7990A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824045 | |||||||
| chr5:56824140 | C | G | 3 | a0003c0002t0003g0039 a0003c0002t0004g0038 a0003c0002t0007g0037 |
3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+8085C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824140 | |||||||
| chr5:56824326 | G | A | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+8271G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824326 | |||||||
| chr5:56824419 | T | C | 1 | a0001c0005t0004g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.482+8364T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824419 | |||||||
| chr5:56824523 | A | C | 4 | a0002c0003t0001g0009 a0002c0003t0001g0019 a0002c0003t0001g0139 others(1): Show |
7 | HG01884.hp1 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.482+8468A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824523 | |||||||
| chr5:56824528 | A | G | 45 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(42): Show |
51 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.482+8473A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824528 | |||||||
| chr5:56824546 | G | A | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.482+8491G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824546 | |||||||
| chr5:56824586 | C | T | 217 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(214): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.482+8531C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824586 | |||||||
| chr5:56824597 | A | G | 1 | a0002c0004t0004g0120 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.482+8542A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824597 | |||||||
| chr5:56824625 | T | G | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+8570T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824625 | |||||||
| chr5:56824819 | G | A | 83 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(80): Show |
91 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.482+8764G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824819 | |||||||
| chr5:56824859 | T | C | 83 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(80): Show |
91 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.482+8804T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824859 | |||||||
| chr5:56824919 | C | G | 3 | a0001c0005t0003g0228 a0001c0005t0003g0229 a0001c0005t0003g0230 |
3 | HG03831.hp2 NA18968.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.482+8864C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824919 | |||||||
| chr5:56824933 | T | A | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+8878T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824933 | |||||||
| chr5:56824942 | T | A | 216 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(213): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.482+8887T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824942 | |||||||
| chr5:56824943 | T | A | 156 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(153): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.482+8888T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824943 | |||||||
| chr5:56824967 | G | A | 1 | a0001c0001t0002g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.482+8912G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824967 | |||||||
| chr5:56824976 | A | G | 1 | a0001c0001t0002g0309 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.482+8921A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56824976 | |||||||
| chr5:56825170 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.482+9115A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825170 | |||||||
| chr5:56825304 | T | C | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.482+9249T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825304 | |||||||
| chr5:56825416 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.482+9361G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825416 | |||||||
| chr5:56825635 | T | C | 3 | a0003c0002t0003g0039 a0003c0002t0004g0038 a0003c0002t0007g0037 |
3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+9580T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825635 | |||||||
| chr5:56825785 | C | T | 1 | a0002c0004t0003g0119 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.482+9730C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825785 | |||||||
| chr5:56825821 | C | A | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+9766C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825821 | |||||||
| chr5:56825927 | A | G | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.482+9872A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825927 | |||||||
| chr5:56825959 | C | T | 3 | a0001c0011t0007g0199 a0003c0002t0001g0189 a0003c0002t0001g0190 |
3 | HG00099.hp1 HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.482+9904C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825959 | |||||||
| chr5:56825961 | G | C | 217 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(214): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.482+9906G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56825961 | |||||||
| chr5:56825967 | CT | C | 64 | a0001c0001t0002g0260 a0002c0003t0001g0049 a0002c0003t0001g0050 others(61): Show |
71 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.482+9924delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56825967 | ||||||
| chr5:56826006 | T | G | 1 | a0002c0004t0001g0051 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.482+9951T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56826006 | |||||||
| chr5:56826395 | G | C | 1 | a0001c0001t0002g0261 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.482+10340G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56826395 | |||||||
| chr5:56826475 | C | CA | 3 | a0001c0005t0003g0214 a0001c0005t0003g0215 a0001c0005t0003g0216 |
3 | NA18948.hp1 NA19060.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.482+10421dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56826475 | ||||||
| chr5:56826489 | CAGGGAA | C | 83 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(80): Show |
91 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.482+10436_482+1044 others(10): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56826489 | ||||||
| chr5:56826517 | A | G | 42 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(39): Show |
46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.482+10462A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56826517 | |||||||
| chr5:56826529 | T | A | 1 | a0002c0003t0001g0052 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.482+10474T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56826529 | |||||||
| chr5:56826664 | C | T | 2 | a0001c0006t0003g0246 a0001c0006t0003g0247 |
2 | NA18956.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.482+10609C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56826664 | |||||||
| chr5:56826749 | G | A | 6 | a0003c0002t0006g0014 a0003c0002t0006g0040 a0003c0002t0006g0041 others(3): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+10694G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56826749 | |||||||
| chr5:56826817 | G | T | 1 | a0003c0002t0001g0175 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.482+10762G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56826817 | |||||||
| chr5:56827064 | G | A | 1 | a0003c0002t0001g0181 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.482+11009G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827064 | |||||||
| chr5:56827096 | C | T | 1 | a0001c0001t0011g0320 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.482+11041C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827096 | |||||||
| chr5:56827189 | A | AGCTG | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.482+11136_482+1113 others(8): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56827189 | ||||||
| chr5:56827218 | G | A | 1 | a0002c0003t0001g0053 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.482+11163G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827218 | |||||||
| chr5:56827231 | G | A | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+11176G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827231 | |||||||
| chr5:56827260 | C | T | 1 | a0003c0002t0001g0031 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.482+11205C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827260 | |||||||
| chr5:56827282 | C | T | 1 | a0003c0002t0001g0032 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.482+11227C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827282 | |||||||
| chr5:56827605 | C | T | 83 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(80): Show |
91 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.482+11550C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827605 | |||||||
| chr5:56827616 | T | C | 331 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(328): Show |
371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.482+11561T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827616 | |||||||
| chr5:56827678 | A | T | 12 | a0002c0003t0001g0017 a0002c0003t0001g0115 a0002c0003t0001g0116 others(9): Show |
13 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.482+11623A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827678 | |||||||
| chr5:56827752 | T | C | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+11697T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827752 | |||||||
| chr5:56827864 | C | CA | 13 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(10): Show |
14 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.482+11821dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56827864 | ||||||
| chr5:56827875 | A | T | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.482+11820A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827875 | |||||||
| chr5:56827919 | C | T | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.482+11864C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56827919 | |||||||
| chr5:56828038 | T | TA | 3 | a0003c0002t0003g0039 a0003c0002t0004g0038 a0003c0002t0007g0037 |
3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+11984dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56828038 | ||||||
| chr5:56828130 | A | G | 2 | a0003c0002t0006g0035 a0003c0002t0006g0036 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.482+12075A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828130 | |||||||
| chr5:56828197 | G | A | 1 | a0002c0007t0001g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.482+12142G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828197 | |||||||
| chr5:56828284 | T | C | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.482+12229T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828284 | |||||||
| chr5:56828526 | A | G | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+12471A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828526 | |||||||
| chr5:56828596 | T | A | 217 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(214): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.482+12541T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828596 | |||||||
| chr5:56828622 | A | G | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.482+12567A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828622 | |||||||
| chr5:56828788 | G | A | 8 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0006g0014 others(5): Show |
9 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.482+12733G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828788 | |||||||
| chr5:56828809 | TA | T | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+12760delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56828809 | ||||||
| chr5:56828816 | G | T | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+12761G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828816 | |||||||
| chr5:56828828 | ACTT | A | 3 | a0001c0005t0001g0227 a0002c0003t0005g0131 a0002c0003t0005g0132 |
3 | HG00673.hp2 HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.482+12780_482+1278 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56828828 | ||||||
| chr5:56828882 | CTTTTT | C | 217 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(214): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.482+12833_482+1283 others(9): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56828882 | ||||||
| chr5:56828902 | A | G | 2 | a0003c0002t0006g0035 a0003c0002t0006g0036 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.482+12847A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828902 | |||||||
| chr5:56828967 | G | C | 42 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(39): Show |
46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.482+12912G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56828967 | |||||||
| chr5:56829287 | A | G | 1 | a0001c0001t0009g0328 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.482+13232A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56829287 | |||||||
| chr5:56829349 | A | AT | 147 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(144): Show |
162 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.482+13313dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56829349 | ||||||
| chr5:56829349 | A | ATT | 8 | a0001c0001t0002g0213 a0001c0001t0002g0261 a0001c0001t0002g0308 others(5): Show |
8 | HG02056.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.482+13312_482+1331 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56829349 | ||||||
| chr5:56829437 | C | T | 1 | a0002c0003t0001g0107 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.482+13382C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56829437 | |||||||
| chr5:56829526 | A | G | 80 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(77): Show |
88 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.482+13471A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56829526 | |||||||
| chr5:56829529 | A | T | 1 | a0003c0002t0004g0186 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.482+13474A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56829529 | |||||||
| chr5:56829662 | T | C | 2 | a0002c0003t0001g0055 a0002c0003t0006g0056 |
2 | HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.482+13607T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56829662 | |||||||
| chr5:56829698 | G | A | 1 | a0001c0001t0009g0321 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.482+13643G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56829698 | |||||||
| chr5:56829869 | T | A | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.482+13814T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56829869 | |||||||
| chr5:56830077 | T | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(82): Show |
93 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.482+14022T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56830077 | |||||||
| chr5:56830101 | G | T | 5 | a0001c0005t0007g0313 a0001c0005t0007g0314 a0001c0005t0007g0315 others(2): Show |
5 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.482+14046G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56830101 | |||||||
| chr5:56830164 | A | G | 2 | a0001c0001t0008g0307 a0001c0001t0010g0306 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.482+14109A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56830164 | |||||||
| chr5:56830813 | A | G | 4 | a0002c0004t0001g0104 a0002c0004t0001g0105 a0002c0004t0001g0106 others(1): Show |
4 | HG00621.hp2 NA18947.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+14758A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56830813 | |||||||
| chr5:56830885 | G | GT | 11 | a0003c0002t0003g0039 a0003c0002t0004g0038 a0003c0002t0006g0014 others(8): Show |
12 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.482+14840dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56830885 | ||||||
| chr5:56830885 | G | T | 2 | a0003c0002t0001g0031 a0003c0002t0001g0032 |
2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.482+14830G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56830885 | |||||||
| chr5:56830916 | A | AT | 63 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0212 others(60): Show |
70 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.482+14873dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56830916 | ||||||
| chr5:56830964 | A | G | 3 | a0003c0002t0003g0039 a0003c0002t0004g0038 a0003c0002t0007g0037 |
3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+14909A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56830964 | |||||||
| chr5:56831003 | C | T | 1 | a0007c0020t0012g0128 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.482+14948C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831003 | |||||||
| chr5:56831013 | A | G | 59 | a0001c0001t0017g0305 a0002c0004t0004g0103 a0003c0002t0001g0003 others(56): Show |
65 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.482+14958A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831013 | |||||||
| chr5:56831107 | T | C | 4 | a0003c0002t0011g0207 a0003c0009t0001g0029 a0003c0009t0004g0318 others(1): Show |
5 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.482+15052T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831107 | |||||||
| chr5:56831184 | G | GT | 6 | a0002c0003t0001g0002 a0002c0003t0001g0100 a0002c0003t0001g0108 others(3): Show |
6 | HG02622.hp1 HG04115.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.482+15147dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56831184 | ||||||
| chr5:56831184 | GT | G | 120 | a0001c0001t0002g0300 a0001c0001t0007g0327 a0001c0001t0009g0030 others(117): Show |
132 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.482+15147delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56831184 | ||||||
| chr5:56831184 | GTT | G | 95 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(92): Show |
105 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.482+15146_482+1514 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56831184 | ||||||
| chr5:56831286 | A | G | 2 | a0001c0001t0002g0256 a0003c0002t0001g0190 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.482+15231A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831286 | |||||||
| chr5:56831403 | C | G | 1 | a0001c0001t0002g0304 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.482+15348C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831403 | |||||||
| chr5:56831458 | C | T | 1 | a0001c0001t0002g0303 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.482+15403C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831458 | |||||||
| chr5:56831734 | C | T | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+15679C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831734 | |||||||
| chr5:56831852 | C | G | 1 | a0001c0001t0002g0012 | 3 | HG01952.hp2 NA20300.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.482+15797C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831852 | |||||||
| chr5:56831971 | T | C | 3 | a0003c0002t0003g0039 a0003c0002t0004g0038 a0003c0002t0007g0037 |
3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+15916T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56831971 | |||||||
| chr5:56832039 | G | A | 59 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(56): Show |
66 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.482+15984G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832039 | |||||||
| chr5:56832214 | A | C | 2 | a0002c0003t0001g0101 a0002c0003t0005g0102 |
2 | NA18965.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.482+16159A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832214 | |||||||
| chr5:56832258 | G | T | 2 | a0003c0002t0001g0031 a0003c0002t0001g0032 |
2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.482+16203G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832258 | |||||||
| chr5:56832314 | A | G | 3 | a0001c0001t0002g0206 a0001c0001t0002g0259 a0001c0001t0002g0302 |
3 | HG00639.hp2 HG01175.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.482+16259A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832314 | |||||||
| chr5:56832320 | G | A | 6 | a0003c0002t0006g0014 a0003c0002t0006g0040 a0003c0002t0006g0041 others(3): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+16265G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832320 | |||||||
| chr5:56832578 | T | C | 1 | a0003c0002t0001g0179 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.482+16523T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832578 | |||||||
| chr5:56832628 | G | A | 1 | a0002c0003t0001g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.482+16573G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832628 | |||||||
| chr5:56832714 | G | T | 5 | a0001c0005t0007g0313 a0001c0005t0007g0314 a0001c0005t0007g0315 others(2): Show |
5 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.482+16659G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832714 | |||||||
| chr5:56832903 | C | T | 10 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0006g0014 others(7): Show |
11 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.482+16848C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56832903 | |||||||
| chr5:56833021 | A | G | 59 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(56): Show |
65 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.482+16966A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833021 | |||||||
| chr5:56833070 | C | T | 1 | a0001c0005t0003g0226 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.482+17015C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833070 | |||||||
| chr5:56833093 | A | T | 1 | a0008c0017t0002g0301 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.482+17038A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833093 | |||||||
| chr5:56833112 | C | T | 42 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(39): Show |
46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.482+17057C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833112 | |||||||
| chr5:56833149 | C | T | 2 | a0001c0001t0002g0212 a0001c0001t0002g0213 |
2 | HG01109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.482+17094C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833149 | |||||||
| chr5:56833172 | G | C | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.482+17117G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833172 | |||||||
| chr5:56833224 | C | T | 2 | a0003c0002t0001g0173 a0003c0002t0001g0174 |
2 | NA18977.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.482+17169C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833224 | |||||||
| chr5:56833270 | G | A | 4 | a0002c0003t0001g0060 a0002c0003t0001g0062 a0002c0003t0001g0108 others(1): Show |
4 | HG00642.hp1 HG01346.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+17215G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833270 | |||||||
| chr5:56833333 | G | A | 1 | a0002c0004t0001g0063 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.482+17278G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833333 | |||||||
| chr5:56833358 | A | G | 3 | a0003c0002t0003g0039 a0003c0002t0004g0038 a0003c0002t0007g0037 |
3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+17303A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833358 | |||||||
| chr5:56833499 | A | G | 4 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(1): Show |
4 | HG00735.hp2 HG01516.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+17444A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833499 | |||||||
| chr5:56833507 | A | G | 1 | a0001c0001t0008g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.482+17452A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833507 | |||||||
| chr5:56833533 | C | T | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.482+17478C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833533 | |||||||
| chr5:56833869 | T | G | 1 | a0001c0001t0002g0308 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.482+17814T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833869 | |||||||
| chr5:56833942 | G | A | 1 | a0001c0008t0007g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.482+17887G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833942 | |||||||
| chr5:56833976 | T | A | 59 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(56): Show |
65 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.482+17921T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56833976 | |||||||
| chr5:56834139 | G | GTAA | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.482+18086_482+1808 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56834139 | ||||||
| chr5:56834150 | C | A | 1 | a0001c0001t0002g0262 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.482+18095C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834150 | |||||||
| chr5:56834311 | G | C | 1 | a0001c0001t0002g0303 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.482+18256G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834311 | |||||||
| chr5:56834413 | A | G | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+18358A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834413 | |||||||
| chr5:56834436 | G | A | 1 | a0003c0002t0001g0151 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.482+18381G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834436 | |||||||
| chr5:56834495 | T | C | 265 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(262): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.482+18440T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834495 | |||||||
| chr5:56834707 | T | G | 42 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(39): Show |
46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.482+18652T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834707 | |||||||
| chr5:56834713 | CAAA | C | 4 | a0001c0005t0007g0314 a0001c0005t0007g0315 a0001c0005t0007g0316 others(1): Show |
4 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+18659_482+1866 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834713 | |||||||
| chr5:56834844 | A | ATTT | 5 | a0001c0005t0007g0313 a0001c0005t0007g0314 a0001c0005t0007g0315 others(2): Show |
5 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.482+18791_482+1879 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56834844 | ||||||
| chr5:56834856 | T | C | 14 | a0001c0001t0002g0025 a0001c0001t0002g0263 a0001c0001t0002g0264 others(11): Show |
15 | HG00438.hp1 HG01175.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.482+18801T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56834856 | |||||||
| chr5:56835097 | T | G | 20 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(17): Show |
21 | HG00673.hp2 HG02080.hp1 HG02698.hp2 others(18): Show |
intron_variant | MODIFIER | c.482+19042T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835097 | |||||||
| chr5:56835284 | A | AGACAGGA others(59): Show |
2 | a0002c0003t0005g0133 a0002c0003t0020g0123 |
2 | NA18942.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.482+19344_482+1940 others(70): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835284 | ||||||
| chr5:56835284 | AGACAGGA others(59): Show |
A | 199 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(196): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.482+19344_482+1940 others(70): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835284 | ||||||
| chr5:56835289 | G | A | 1 | a0001c0001t0011g0320 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.482+19234G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835289 | |||||||
| chr5:56835306 | AGACAGGA others(37): Show |
A | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.482+19278_482+1932 others(48): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835306 | ||||||
| chr5:56835319 | G | A | 1 | a0002c0003t0005g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19264G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835319 | |||||||
| chr5:56835323 | A | G | 1 | a0002c0003t0005g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19268A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835323 | |||||||
| chr5:56835324 | G | C | 1 | a0002c0003t0005g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19269G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835324 | |||||||
| chr5:56835325 | A | C | 1 | a0002c0003t0005g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19270A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835325 | |||||||
| chr5:56835326 | G | T | 1 | a0002c0003t0005g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19271G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835326 | |||||||
| chr5:56835331 | CAAGGAGG others(56): Show |
C | 1 | a0003c0002t0001g0191 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.482+19277_482+1933 others(67): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835331 | |||||||
| chr5:56835332 | A | C | 1 | a0002c0003t0005g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19277A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835332 | |||||||
| chr5:56835336 | A | C | 1 | a0002c0003t0005g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19281A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835336 | |||||||
| chr5:56835337 | G | T | 1 | a0002c0003t0005g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19282G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835337 | |||||||
| chr5:56835345 | A | T | 1 | a0002c0003t0005g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19290A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835345 | |||||||
| chr5:56835346 | G | T | 1 | a0002c0003t0005g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19291G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835346 | |||||||
| chr5:56835349 | T | G | 1 | a0002c0003t0005g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19294T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835349 | |||||||
| chr5:56835350 | T | A | 1 | a0002c0003t0005g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.482+19295T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835350 | |||||||
| chr5:56835350 | TGACAGGA others(81): Show |
T | 11 | a0001c0001t0002g0262 a0001c0001t0007g0327 a0001c0001t0009g0030 others(8): Show |
12 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.482+19328_482+1941 others(92): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835350 | ||||||
| chr5:56835357 | AAGGCAGG others(37): Show |
A | 2 | a0003c0002t0003g0039 a0003c0002t0004g0038 |
2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.482+19316_482+1935 others(48): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835357 | ||||||
| chr5:56835372 | A | AGACAGGA others(15): Show |
2 | a0001c0001t0002g0210 a0001c0001t0008g0209 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.482+19337_482+1933 others(26): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835372 | ||||||
| chr5:56835372 | AGACAGGA others(37): Show |
A | 1 | a0001c0001t0017g0305 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.482+19344_482+1938 others(48): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835372 | ||||||
| chr5:56835393 | G | T | 10 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0006g0014 others(7): Show |
11 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.482+19338G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835393 | |||||||
| chr5:56835394 | A | T | 10 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0006g0014 others(7): Show |
11 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.482+19339A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835394 | |||||||
| chr5:56835394 | AGACAAGG others(15): Show |
A | 1 | a0001c0001t0010g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.482+19344_482+1936 others(26): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835394 | ||||||
| chr5:56835399 | A | G | 12 | a0001c0001t0002g0210 a0001c0001t0008g0209 a0003c0002t0001g0031 others(9): Show |
13 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.482+19344A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835399 | |||||||
| chr5:56835401 | G | A | 12 | a0001c0001t0002g0210 a0001c0001t0008g0209 a0003c0002t0001g0031 others(9): Show |
13 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.482+19346G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835401 | |||||||
| chr5:56835413 | A | G | 5 | a0001c0005t0003g0223 a0001c0005t0003g0224 a0001c0005t0003g0228 others(2): Show |
5 | HG03831.hp2 NA18960.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.482+19358A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835413 | |||||||
| chr5:56835416 | TGACAGGA others(15): Show |
T | 1 | a0002c0004t0003g0119 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.482+19394_482+1941 others(26): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56835416 | ||||||
| chr5:56835523 | G | T | 59 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(56): Show |
66 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.482+19468G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835523 | |||||||
| chr5:56835594 | A | G | 331 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(328): Show |
371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.482+19539A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835594 | |||||||
| chr5:56835608 | T | A | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.482+19553T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835608 | |||||||
| chr5:56835702 | G | C | 1 | a0003c0002t0001g0031 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.482+19647G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835702 | |||||||
| chr5:56835725 | G | A | 1 | a0003c0002t0001g0032 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.482+19670G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835725 | |||||||
| chr5:56835978 | T | A | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.482+19923T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56835978 | |||||||
| chr5:56836288 | C | G | 98 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(95): Show |
107 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.482+20233C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56836288 | |||||||
| chr5:56836327 | A | AG | 265 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(262): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.482+20272_483-2027 others(5): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56836327 | |||||||
| chr5:56836353 | G | A | 1 | a0008c0017t0002g0301 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.483-20247G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56836353 | |||||||
| chr5:56836621 | G | A | 1 | a0003c0002t0007g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483-19979G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56836621 | |||||||
| chr5:56836629 | G | C | 1 | a0002c0003t0001g0060 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.483-19971G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56836629 | |||||||
| chr5:56836800 | T | C | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.483-19800T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56836800 | |||||||
| chr5:56837039 | A | G | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-19561A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837039 | |||||||
| chr5:56837049 | C | G | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-19551C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837049 | |||||||
| chr5:56837212 | A | G | 1 | a0001c0001t0002g0296 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.483-19388A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837212 | |||||||
| chr5:56837391 | T | C | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-19209T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837391 | |||||||
| chr5:56837728 | G | A | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.483-18872G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837728 | |||||||
| chr5:56837786 | C | T | 1 | a0001c0011t0007g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.483-18814C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837786 | |||||||
| chr5:56837921 | G | C | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(83): Show |
94 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.483-18679G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837921 | |||||||
| chr5:56837934 | G | A | 1 | a0002c0003t0006g0117 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.483-18666G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56837934 | |||||||
| chr5:56838040 | T | G | 2 | a0003c0002t0001g0177 a0003c0002t0011g0207 |
2 | NA18986.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.483-18560T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838040 | |||||||
| chr5:56838127 | G | C | 1 | a0003c0002t0001g0175 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.483-18473G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838127 | |||||||
| chr5:56838243 | T | TTC | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.483-18356_483-1835 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56838243 | ||||||
| chr5:56838317 | A | G | 6 | a0003c0002t0006g0014 a0003c0002t0006g0040 a0003c0002t0006g0041 others(3): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.483-18283A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838317 | |||||||
| chr5:56838342 | A | C | 3 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0213 |
3 | HG01109.hp1 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.483-18258A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838342 | |||||||
| chr5:56838380 | A | G | 2 | a0003c0002t0003g0039 a0003c0002t0004g0038 |
2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.483-18220A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838380 | |||||||
| chr5:56838449 | A | G | 42 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(39): Show |
46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.483-18151A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838449 | |||||||
| chr5:56838476 | T | A | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-18124T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838476 | |||||||
| chr5:56838539 | G | A | 1 | a0001c0005t0007g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.483-18061G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838539 | |||||||
| chr5:56838733 | T | G | 22 | a0001c0006t0001g0237 a0001c0006t0003g0024 a0001c0006t0003g0233 others(19): Show |
25 | HG00423.hp2 HG01261.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.483-17867T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838733 | |||||||
| chr5:56838895 | T | TTTTTG | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-17689_483-1768 others(9): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56838895 | ||||||
| chr5:56838943 | T | C | 2 | a0001c0001t0002g0212 a0001c0001t0002g0213 |
2 | HG01109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.483-17657T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838943 | |||||||
| chr5:56838995 | C | A | 3 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0213 |
3 | HG01109.hp1 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.483-17605C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56838995 | |||||||
| chr5:56839008 | G | A | 1 | a0001c0006t0003g0233 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.483-17592G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839008 | |||||||
| chr5:56839037 | T | C | 1 | a0005c0012t0008g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.483-17563T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839037 | |||||||
| chr5:56839072 | G | C | 1 | a0002c0003t0001g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.483-17528G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839072 | |||||||
| chr5:56839099 | G | C | 1 | a0002c0003t0012g0086 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.483-17501G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839099 | |||||||
| chr5:56839219 | C | T | 1 | a0008c0017t0002g0301 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.483-17381C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839219 | |||||||
| chr5:56839238 | T | C | 4 | a0005c0012t0008g0057 a0005c0012t0008g0059 a0005c0012t0010g0058 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-17362T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839238 | |||||||
| chr5:56839429 | T | A | 1 | a0002c0007t0001g0087 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.483-17171T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839429 | |||||||
| chr5:56839627 | A | G | 1 | a0002c0003t0001g0009 | 3 | HG02486.hp2 HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.483-16973A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839627 | |||||||
| chr5:56839719 | T | C | 3 | a0002c0003t0001g0088 a0002c0003t0001g0089 a0002c0003t0001g0122 |
3 | HG02976.hp1 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.483-16881T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839719 | |||||||
| chr5:56839750 | A | G | 2 | a0003c0002t0003g0039 a0003c0002t0004g0038 |
2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.483-16850A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839750 | |||||||
| chr5:56839815 | A | C | 1 | a0002c0003t0001g0107 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.483-16785A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839815 | |||||||
| chr5:56839904 | C | CTTG | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.483-16694_483-1669 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56839904 | ||||||
| chr5:56839978 | C | T | 2 | a0001c0001t0002g0212 a0001c0001t0002g0213 |
2 | HG01109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.483-16622C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839978 | |||||||
| chr5:56839989 | G | T | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-16611G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839989 | |||||||
| chr5:56839998 | T | A | 1 | a0002c0003t0001g0109 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.483-16602T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56839998 | |||||||
| chr5:56840246 | C | G | 1 | a0001c0001t0002g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.483-16354C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840246 | |||||||
| chr5:56840408 | A | G | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(83): Show |
94 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.483-16192A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840408 | |||||||
| chr5:56840448 | AAAT | A | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-16148_483-1614 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56840448 | ||||||
| chr5:56840513 | C | T | 1 | a0003c0002t0001g0185 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.483-16087C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840513 | |||||||
| chr5:56840516 | G | T | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.483-16084G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840516 | |||||||
| chr5:56840588 | C | A | 1 | a0001c0006t0003g0233 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.483-16012C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840588 | |||||||
| chr5:56840665 | A | G | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(83): Show |
94 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.483-15935A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840665 | |||||||
| chr5:56840737 | C | G | 1 | a0003c0002t0001g0144 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.483-15863C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840737 | |||||||
| chr5:56840741 | T | C | 3 | a0003c0002t0003g0039 a0003c0002t0004g0038 a0003c0002t0007g0037 |
3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.483-15859T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840741 | |||||||
| chr5:56840776 | C | G | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-15824C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56840776 | |||||||
| chr5:56840870 | G | GT | 67 | a0001c0001t0002g0025 a0001c0001t0002g0295 a0001c0006t0003g0243 others(64): Show |
75 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.483-15712dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56840870 | ||||||
| chr5:56840870 | GT | G | 18 | a0001c0001t0010g0268 a0001c0006t0003g0252 a0001c0008t0007g0022 others(15): Show |
19 | HG01081.hp2 HG01496.hp1 HG02717.hp1 others(16): Show |
intron_variant | MODIFIER | c.483-15712delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56840870 | ||||||
| chr5:56841025 | A | G | 1 | a0001c0001t0002g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.483-15575A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841025 | |||||||
| chr5:56841201 | T | TAA | 6 | a0001c0001t0002g0255 a0001c0001t0002g0269 a0001c0001t0002g0270 others(3): Show |
6 | HG02683.hp2 HG03654.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.483-15399_483-1539 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841201 | |||||||
| chr5:56841202 | T | A | 7 | a0001c0001t0002g0255 a0001c0001t0002g0269 a0001c0001t0002g0270 others(4): Show |
7 | HG02683.hp2 HG03654.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.483-15398T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841202 | |||||||
| chr5:56841202 | T | TA | 39 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0213 others(36): Show |
42 | HG00423.hp2 HG01109.hp1 HG01256.hp2 others(39): Show |
intron_variant | MODIFIER | c.483-15384dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56841202 | ||||||
| chr5:56841202 | T | TAA | 64 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(61): Show |
72 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.483-15385_483-1538 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56841202 | ||||||
| chr5:56841202 | TA | T | 42 | a0001c0005t0003g0230 a0002c0004t0001g0001 a0002c0004t0001g0006 others(39): Show |
49 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.483-15384delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56841202 | ||||||
| chr5:56841273 | T | G | 1 | a0002c0004t0001g0067 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.483-15327T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841273 | |||||||
| chr5:56841278 | C | T | 5 | a0001c0005t0007g0313 a0001c0005t0007g0314 a0001c0005t0007g0315 others(2): Show |
5 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.483-15322C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841278 | |||||||
| chr5:56841343 | G | C | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.483-15257G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841343 | |||||||
| chr5:56841386 | T | C | 2 | a0001c0005t0003g0223 a0001c0005t0003g0224 |
2 | NA18960.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.483-15214T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841386 | |||||||
| chr5:56841407 | C | T | 1 | a0001c0006t0003g0242 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.483-15193C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841407 | |||||||
| chr5:56841408 | G | C | 1 | a0003c0002t0001g0154 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.483-15192G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841408 | |||||||
| chr5:56841427 | A | G | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.483-15173A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841427 | |||||||
| chr5:56841487 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.483-15113T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841487 | |||||||
| chr5:56841541 | GGATTATA others(4): Show |
G | 1 | a0003c0002t0001g0151 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.483-15056_483-1504 others(15): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56841541 | ||||||
| chr5:56841605 | C | T | 61 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(58): Show |
68 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.483-14995C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841605 | |||||||
| chr5:56841626 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.483-14974C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841626 | |||||||
| chr5:56841630 | T | C | 3 | a0002c0003t0001g0053 a0002c0003t0001g0091 a0002c0003t0001g0092 |
3 | HG02559.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.483-14970T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841630 | |||||||
| chr5:56841960 | G | A | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.483-14640G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56841960 | |||||||
| chr5:56842009 | C | T | 1 | a0002c0004t0001g0082 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.483-14591C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56842009 | |||||||
| chr5:56842261 | A | G | 1 | a0001c0001t0002g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.483-14339A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56842261 | |||||||
| chr5:56842507 | C | T | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.483-14093C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56842507 | |||||||
| chr5:56842650 | T | C | 1 | a0001c0001t0009g0030 | 2 | HG02572.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.483-13950T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56842650 | |||||||
| chr5:56842655 | C | T | 10 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0006g0014 others(7): Show |
11 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.483-13945C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56842655 | |||||||
| chr5:56842951 | C | T | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-13649C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56842951 | |||||||
| chr5:56843147 | G | T | 1 | a0003c0002t0001g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.483-13453G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843147 | |||||||
| chr5:56843255 | C | T | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-13345C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843255 | |||||||
| chr5:56843355 | C | G | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-13245C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843355 | |||||||
| chr5:56843366 | A | T | 1 | a0003c0002t0001g0182 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.483-13234A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843366 | |||||||
| chr5:56843373 | T | C | 1 | a0002c0003t0001g0055 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.483-13227T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843373 | |||||||
| chr5:56843419 | T | C | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-13181T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843419 | |||||||
| chr5:56843444 | C | T | 1 | a0003c0009t0004g0319 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.483-13156C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843444 | |||||||
| chr5:56843482 | A | T | 2 | a0003c0002t0006g0035 a0003c0002t0006g0036 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.483-13118A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843482 | |||||||
| chr5:56843507 | G | C | 1 | a0001c0001t0002g0254 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.483-13093G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843507 | |||||||
| chr5:56843512 | A | G | 1 | a0002c0003t0001g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.483-13088A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843512 | |||||||
| chr5:56843717 | G | A | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.483-12883G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843717 | |||||||
| chr5:56843746 | T | C | 1 | a0001c0001t0008g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.483-12854T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843746 | |||||||
| chr5:56843930 | C | G | 1 | a0002c0003t0001g0089 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.483-12670C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843930 | |||||||
| chr5:56843963 | C | T | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-12637C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56843963 | |||||||
| chr5:56844082 | T | C | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-12518T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844082 | |||||||
| chr5:56844094 | A | G | 2 | a0003c0002t0006g0035 a0003c0002t0006g0036 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.483-12506A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844094 | |||||||
| chr5:56844177 | T | A | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-12423T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844177 | |||||||
| chr5:56844182 | G | GT | 2 | a0001c0006t0003g0024 a0001c0006t0003g0247 |
3 | HG01516.hp1 HG01517.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.483-12418_483-1241 others(5): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844182 | |||||||
| chr5:56844183 | G | GT | 113 | a0001c0001t0002g0026 a0001c0001t0002g0211 a0001c0001t0002g0213 others(110): Show |
129 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.483-12393dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56844183 | ||||||
| chr5:56844183 | G | GTT | 67 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0027 others(64): Show |
74 | HG00099.hp2 HG00639.hp2 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.483-12394_483-1239 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56844183 | ||||||
| chr5:56844183 | G | GTTT | 20 | a0001c0001t0002g0025 a0001c0001t0002g0028 a0001c0001t0002g0205 others(17): Show |
22 | HG00438.hp1 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.483-12395_483-1239 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56844183 | ||||||
| chr5:56844183 | G | T | 8 | a0001c0006t0003g0024 a0001c0006t0003g0241 a0001c0006t0003g0246 others(5): Show |
10 | HG01243.hp2 HG01361.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.483-12417G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844183 | |||||||
| chr5:56844183 | GT | G | 9 | a0001c0008t0007g0022 a0001c0008t0007g0204 a0001c0008t0011g0203 others(6): Show |
10 | HG01081.hp2 HG01169.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.483-12393delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56844183 | ||||||
| chr5:56844183 | GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0008g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.483-12407_483-1239 others(19): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56844183 | ||||||
| chr5:56844229 | G | A | 1 | a0003c0002t0007g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483-12371G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844229 | |||||||
| chr5:56844304 | C | T | 2 | a0003c0002t0007g0037 a0003c0002t0011g0207 |
2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.483-12296C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844304 | |||||||
| chr5:56844336 | T | C | 1 | a0002c0004t0001g0045 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.483-12264T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844336 | |||||||
| chr5:56844374 | T | C | 266 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(263): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.483-12226T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844374 | |||||||
| chr5:56844383 | G | C | 1 | a0002c0003t0001g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.483-12217G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844383 | |||||||
| chr5:56844415 | G | A | 1 | a0001c0005t0007g0314 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.483-12185G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844415 | |||||||
| chr5:56844422 | G | A | 1 | a0001c0001t0017g0305 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.483-12178G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844422 | |||||||
| chr5:56844430 | T | C | 1 | a0001c0001t0017g0305 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.483-12170T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844430 | |||||||
| chr5:56844452 | T | G | 1 | a0003c0002t0003g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.483-12148T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844452 | |||||||
| chr5:56844458 | T | C | 1 | a0003c0002t0001g0155 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.483-12142T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844458 | |||||||
| chr5:56844460 | T | A | 1 | a0002c0004t0001g0063 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.483-12140T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844460 | |||||||
| chr5:56844511 | G | C | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.483-12089G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844511 | |||||||
| chr5:56844599 | T | C | 1 | a0003c0002t0003g0039 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.483-12001T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844599 | |||||||
| chr5:56844641 | C | T | 1 | a0003c0002t0003g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.483-11959C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844641 | |||||||
| chr5:56844646 | G | A | 1 | a0007c0020t0012g0128 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.483-11954G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844646 | |||||||
| chr5:56844831 | C | T | 3 | a0001c0001t0002g0304 a0001c0001t0008g0267 a0001c0001t0015g0265 |
3 | HG00438.hp1 NA18960.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.483-11769C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844831 | |||||||
| chr5:56844859 | AAAG | A | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-11735_483-1173 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56844859 | ||||||
| chr5:56844900 | A | G | 41 | a0002c0004t0001g0001 a0002c0004t0001g0006 a0002c0004t0001g0015 others(38): Show |
48 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.483-11700A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844900 | |||||||
| chr5:56844991 | C | T | 1 | a0001c0001t0002g0303 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.483-11609C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56844991 | |||||||
| chr5:56845076 | T | G | 1 | a0001c0001t0002g0310 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.483-11524T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845076 | |||||||
| chr5:56845126 | A | G | 3 | a0003c0002t0003g0039 a0003c0002t0004g0038 a0003c0002t0007g0037 |
3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.483-11474A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845126 | |||||||
| chr5:56845206 | A | G | 1 | a0006c0013t0002g0294 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.483-11394A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845206 | |||||||
| chr5:56845328 | A | G | 22 | a0001c0006t0001g0237 a0001c0006t0003g0024 a0001c0006t0003g0233 others(19): Show |
25 | HG00423.hp2 HG01261.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.483-11272A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845328 | |||||||
| chr5:56845420 | CA | C | 9 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(6): Show |
10 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.483-11179delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845420 | |||||||
| chr5:56845532 | C | CTCTCTAG others(21): Show |
2 | a0003c0002t0007g0037 a0003c0002t0011g0207 |
2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.483-11066_483-1103 others(32): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56845532 | ||||||
| chr5:56845540 | G | T | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-11060G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845540 | |||||||
| chr5:56845568 | T | G | 1 | a0002c0004t0001g0077 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.483-11032T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845568 | |||||||
| chr5:56845685 | C | T | 2 | a0003c0002t0001g0031 a0003c0002t0001g0032 |
2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.483-10915C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845685 | |||||||
| chr5:56845709 | A | T | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.483-10891A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845709 | |||||||
| chr5:56845802 | G | A | 1 | a0001c0001t0002g0254 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.483-10798G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845802 | |||||||
| chr5:56845843 | G | A | 1 | a0001c0001t0008g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.483-10757G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845843 | |||||||
| chr5:56845950 | G | C | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.483-10650G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845950 | |||||||
| chr5:56845958 | A | G | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-10642A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56845958 | |||||||
| chr5:56846100 | G | A | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.483-10500G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846100 | |||||||
| chr5:56846169 | A | C | 1 | a0003c0002t0003g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.483-10431A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846169 | |||||||
| chr5:56846239 | G | A | 1 | a0003c0002t0007g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483-10361G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846239 | |||||||
| chr5:56846304 | G | C | 1 | a0001c0001t0002g0025 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.483-10296G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846304 | |||||||
| chr5:56846534 | A | G | 4 | a0003c0002t0001g0153 a0003c0002t0001g0164 a0003c0002t0001g0169 others(1): Show |
4 | NA18975.hp2 NA19056.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-10066A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846534 | |||||||
| chr5:56846554 | A | G | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.483-10046A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846554 | |||||||
| chr5:56846610 | G | A | 1 | a0001c0001t0008g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.483-9990G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846610 | |||||||
| chr5:56846720 | G | C | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.483-9880G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846720 | |||||||
| chr5:56846774 | G | A | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.483-9826G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846774 | |||||||
| chr5:56846816 | A | C | 4 | a0001c0011t0007g0198 a0001c0011t0007g0199 a0001c0011t0007g0200 others(1): Show |
4 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-9784A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846816 | |||||||
| chr5:56846866 | T | G | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.483-9734T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846866 | |||||||
| chr5:56846875 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.483-9725C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56846875 | |||||||
| chr5:56846993 | CTACATT | C | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-9605_483-9600d others(8): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56846993 | ||||||
| chr5:56847034 | A | G | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-9566A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847034 | |||||||
| chr5:56847172 | C | T | 42 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(39): Show |
46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.483-9428C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847172 | |||||||
| chr5:56847318 | C | T | 1 | a0001c0011t0007g0199 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.483-9282C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847318 | |||||||
| chr5:56847319 | G | A | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-9281G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847319 | |||||||
| chr5:56847332 | C | T | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-9268C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847332 | |||||||
| chr5:56847390 | A | C | 42 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(39): Show |
46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.483-9210A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847390 | |||||||
| chr5:56847592 | T | C | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(83): Show |
94 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.483-9008T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847592 | |||||||
| chr5:56847609 | A | G | 1 | a0005c0015t0008g0208 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.483-8991A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847609 | |||||||
| chr5:56847964 | A | G | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-8636A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56847964 | |||||||
| chr5:56848058 | A | G | 1 | a0002c0004t0003g0076 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.483-8542A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848058 | |||||||
| chr5:56848091 | G | A | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.483-8509G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848091 | |||||||
| chr5:56848102 | C | CA | 146 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(143): Show |
160 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.483-8488dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56848102 | ||||||
| chr5:56848102 | C | CAA | 60 | a0001c0006t0003g0233 a0003c0002t0001g0003 a0003c0002t0001g0010 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-8489_483-8488d others(4): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56848102 | ||||||
| chr5:56848189 | T | C | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-8411T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848189 | |||||||
| chr5:56848230 | T | A | 2 | a0001c0001t0002g0260 a0001c0001t0002g0282 |
2 | HG01256.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.483-8370T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848230 | |||||||
| chr5:56848325 | G | A | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.483-8275G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848325 | |||||||
| chr5:56848409 | T | C | 1 | a0003c0002t0003g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.483-8191T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848409 | |||||||
| chr5:56848437 | C | T | 1 | a0002c0004t0004g0075 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.483-8163C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848437 | |||||||
| chr5:56848509 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.483-8091G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848509 | |||||||
| chr5:56848526 | T | G | 1 | a0003c0002t0001g0034 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.483-8074T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848526 | |||||||
| chr5:56848582 | C | T | 331 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(328): Show |
371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.483-8018C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848582 | |||||||
| chr5:56848701 | T | G | 1 | a0002c0003t0001g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.483-7899T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848701 | |||||||
| chr5:56848775 | G | A | 1 | a0002c0007t0001g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.483-7825G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56848775 | |||||||
| chr5:56849104 | T | C | 1 | a0001c0006t0003g0234 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.483-7496T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849104 | |||||||
| chr5:56849230 | G | T | 160 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(157): Show |
175 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.483-7370G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849230 | |||||||
| chr5:56849241 | T | C | 160 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(157): Show |
175 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.483-7359T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849241 | |||||||
| chr5:56849241 | T | G | 14 | a0003c0002t0001g0179 a0003c0002t0001g0180 a0003c0002t0001g0181 others(11): Show |
14 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.483-7359T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849241 | |||||||
| chr5:56849243 | G | A | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-7357G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849243 | |||||||
| chr5:56849326 | G | A | 2 | a0003c0002t0003g0039 a0003c0002t0004g0038 |
2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.483-7274G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849326 | |||||||
| chr5:56849353 | TA | T | 195 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(192): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.483-7230delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56849353 | ||||||
| chr5:56849355 | A | T | 71 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(68): Show |
79 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.483-7245A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849355 | |||||||
| chr5:56849356 | A | T | 1 | a0001c0001t0002g0260 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.483-7244A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849356 | |||||||
| chr5:56849496 | A | G | 1 | a0002c0004t0004g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.483-7104A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849496 | |||||||
| chr5:56849502 | T | C | 1 | a0003c0002t0001g0033 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.483-7098T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849502 | |||||||
| chr5:56849502 | T | G | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-7098T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849502 | |||||||
| chr5:56849602 | G | A | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-6998G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849602 | |||||||
| chr5:56849719 | G | A | 1 | a0003c0002t0001g0178 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.483-6881G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849719 | |||||||
| chr5:56849754 | GTTTGGT | G | 72 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(69): Show |
80 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.483-6829_483-6824d others(8): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56849754 | ||||||
| chr5:56849783 | G | C | 1 | a0003c0002t0007g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483-6817G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849783 | |||||||
| chr5:56849977 | A | G | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.483-6623A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849977 | |||||||
| chr5:56849985 | C | T | 2 | a0003c0002t0007g0037 a0003c0002t0011g0207 |
2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.483-6615C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56849985 | |||||||
| chr5:56850038 | G | A | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-6562G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56850038 | |||||||
| chr5:56850069 | G | A | 2 | a0001c0005t0003g0225 a0001c0005t0003g0226 |
2 | HG03239.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.483-6531G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56850069 | |||||||
| chr5:56850170 | G | A | 17 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0028 others(14): Show |
23 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.483-6430G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56850170 | |||||||
| chr5:56850203 | T | C | 1 | a0003c0002t0006g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.483-6397T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56850203 | |||||||
| chr5:56850301 | T | A | 1 | a0003c0002t0007g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483-6299T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56850301 | |||||||
| chr5:56850866 | A | G | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.483-5734A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56850866 | |||||||
| chr5:56850989 | C | T | 1 | a0002c0003t0004g0061 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.483-5611C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56850989 | |||||||
| chr5:56851113 | AT | A | 95 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(92): Show |
104 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.483-5483delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56851113 | ||||||
| chr5:56851156 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.483-5444G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851156 | |||||||
| chr5:56851226 | A | G | 225 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(222): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.483-5374A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851226 | |||||||
| chr5:56851304 | C | G | 1 | a0003c0002t0007g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483-5296C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851304 | |||||||
| chr5:56851397 | C | T | 2 | a0003c0002t0006g0035 a0003c0002t0006g0036 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.483-5203C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851397 | |||||||
| chr5:56851595 | A | G | 2 | a0002c0003t0001g0091 a0002c0003t0001g0092 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.483-5005A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851595 | |||||||
| chr5:56851618 | G | A | 4 | a0001c0011t0007g0198 a0001c0011t0007g0199 a0001c0011t0007g0200 others(1): Show |
4 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-4982G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851618 | |||||||
| chr5:56851768 | G | A | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-4832G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851768 | |||||||
| chr5:56851937 | G | A | 1 | a0002c0003t0001g0115 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.483-4663G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56851937 | |||||||
| chr5:56852035 | A | G | 20 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(17): Show |
21 | HG00673.hp2 HG02080.hp1 HG02698.hp2 others(18): Show |
intron_variant | MODIFIER | c.483-4565A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852035 | |||||||
| chr5:56852083 | GA | G | 165 | a0001c0001t0017g0305 a0001c0005t0001g0227 a0001c0005t0003g0023 others(162): Show |
186 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.483-4503delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56852083 | ||||||
| chr5:56852083 | GAA | G | 94 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(91): Show |
103 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.483-4504_483-4503d others(4): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56852083 | ||||||
| chr5:56852085 | A | G | 1 | a0003c0002t0003g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.483-4515A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852085 | |||||||
| chr5:56852086 | A | G | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.483-4514A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852086 | |||||||
| chr5:56852113 | G | A | 3 | a0002c0003t0001g0125 a0002c0003t0012g0124 a0007c0020t0012g0128 |
3 | HG02015.hp2 HG03669.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.483-4487G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852113 | |||||||
| chr5:56852125 | T | C | 7 | a0002c0004t0001g0046 a0002c0004t0001g0063 a0002c0004t0001g0065 others(4): Show |
7 | NA18957.hp2 NA18959.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.483-4475T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852125 | |||||||
| chr5:56852289 | G | A | 3 | a0001c0001t0002g0205 a0001c0001t0002g0272 a0001c0001t0008g0292 |
3 | HG00738.hp2 HG01074.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.483-4311G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852289 | |||||||
| chr5:56852349 | C | T | 2 | a0003c0002t0003g0039 a0003c0002t0004g0038 |
2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.483-4251C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852349 | |||||||
| chr5:56852605 | T | C | 1 | a0002c0004t0001g0142 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.483-3995T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852605 | |||||||
| chr5:56852681 | G | A | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.483-3919G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852681 | |||||||
| chr5:56852783 | C | T | 2 | a0001c0001t0009g0324 a0001c0001t0009g0326 |
2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.483-3817C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852783 | |||||||
| chr5:56852914 | C | A | 81 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(78): Show |
89 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.483-3686C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56852914 | |||||||
| chr5:56853214 | A | G | 13 | a0001c0005t0007g0313 a0001c0005t0007g0314 a0001c0005t0007g0315 others(10): Show |
14 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.483-3386A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56853214 | |||||||
| chr5:56853329 | A | G | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-3271A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56853329 | |||||||
| chr5:56853405 | A | G | 1 | a0001c0001t0002g0296 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.483-3195A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56853405 | |||||||
| chr5:56853580 | G | C | 2 | a0003c0002t0007g0037 a0003c0002t0011g0207 |
2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.483-3020G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56853580 | |||||||
| chr5:56853602 | T | G | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.483-2998T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56853602 | |||||||
| chr5:56853716 | T | C | 1 | a0003c0002t0007g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483-2884T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56853716 | |||||||
| chr5:56853984 | C | T | 1 | a0009c0016t0002g0280 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.483-2616C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56853984 | |||||||
| chr5:56854306 | G | T | 1 | a0001c0001t0002g0210 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.483-2294G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854306 | |||||||
| chr5:56854384 | A | G | 1 | a0001c0001t0002g0293 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.483-2216A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854384 | |||||||
| chr5:56854432 | C | CA | 51 | a0001c0001t0002g0253 a0001c0001t0002g0279 a0001c0001t0002g0291 others(48): Show |
59 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.483-2150dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56854432 | ||||||
| chr5:56854432 | C | CAA | 179 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(176): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.483-2151_483-2150d others(4): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56854432 | ||||||
| chr5:56854432 | C | CAAA | 24 | a0001c0001t0002g0255 a0001c0001t0002g0269 a0001c0001t0002g0270 others(21): Show |
25 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.483-2152_483-2150d others(5): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56854432 | ||||||
| chr5:56854447 | A | G | 1 | a0002c0007t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.483-2153A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854447 | |||||||
| chr5:56854506 | G | A | 2 | a0003c0002t0001g0013 a0003c0002t0001g0033 |
3 | HG00558.hp1 NA18964.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.483-2094G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854506 | |||||||
| chr5:56854710 | A | G | 263 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(260): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.483-1890A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854710 | |||||||
| chr5:56854765 | G | A | 1 | a0001c0001t0002g0025 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.483-1835G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854765 | |||||||
| chr5:56854795 | G | C | 81 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(78): Show |
89 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.483-1805G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854795 | |||||||
| chr5:56854976 | T | G | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.483-1624T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56854976 | |||||||
| chr5:56855133 | CTCCTTTC others(6): Show |
C | 58 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(55): Show |
65 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.483-1466_483-1454d others(15): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855133 | |||||||
| chr5:56855173 | C | T | 6 | a0003c0002t0006g0014 a0003c0002t0006g0040 a0003c0002t0006g0041 others(3): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.483-1427C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855173 | |||||||
| chr5:56855230 | A | T | 1 | a0002c0003t0005g0127 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.483-1370A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855230 | |||||||
| chr5:56855272 | A | G | 17 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0028 others(14): Show |
23 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.483-1328A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855272 | |||||||
| chr5:56855535 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.483-1065C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855535 | |||||||
| chr5:56855685 | GGTATTTC others(5): Show |
G | 2 | a0002c0003t0001g0055 a0002c0003t0006g0056 |
2 | HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.483-904_483-893del others(12): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 56855685 | ||||||
| chr5:56855802 | C | T | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-798C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855802 | |||||||
| chr5:56855848 | A | G | 1 | a0003c0002t0001g0146 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.483-752A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855848 | |||||||
| chr5:56855853 | A | G | 2 | a0001c0001t0002g0255 a0001c0001t0002g0270 |
2 | HG02683.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.483-747A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855853 | |||||||
| chr5:56855917 | G | A | 81 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(78): Show |
89 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.483-683G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56855917 | |||||||
| chr5:56856271 | A | G | 1 | a0001c0006t0003g0238 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.483-329A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56856271 | |||||||
| chr5:56856466 | G | A | 1 | a0003c0002t0001g0184 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.483-134G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56856466 | |||||||
| chr5:56856583 | T | G | 1 | a0002c0004t0003g0076 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.483-17T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56856583 | |||||||
| chr5:56856589 | C | A | 160 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(157): Show |
175 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.483-11C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 1/19 | chr5 | 56856589 | |||||||
| chr5:56856968 | G | A | 18 | a0001c0006t0001g0237 a0001c0006t0003g0024 a0001c0006t0003g0233 others(15): Show |
21 | HG00423.hp2 HG01261.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.633+218G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56856968 | |||||||
| chr5:56857161 | A | G | 5 | a0001c0005t0007g0313 a0001c0005t0007g0314 a0001c0005t0007g0315 others(2): Show |
5 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.633+411A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857161 | |||||||
| chr5:56857214 | A | G | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.633+464A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857214 | |||||||
| chr5:56857265 | A | G | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.633+515A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857265 | |||||||
| chr5:56857393 | T | C | 2 | a0003c0002t0006g0035 a0003c0002t0006g0036 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.633+643T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857393 | |||||||
| chr5:56857539 | G | T | 5 | a0003c0002t0001g0021 a0003c0002t0001g0150 a0003c0002t0001g0151 others(2): Show |
6 | HG00621.hp1 NA18945.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.633+789G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857539 | |||||||
| chr5:56857553 | C | T | 2 | a0003c0002t0001g0184 a0003c0002t0001g0185 |
2 | NA18963.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.633+803C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857553 | |||||||
| chr5:56857565 | T | C | 42 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(39): Show |
46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.633+815T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857565 | |||||||
| chr5:56857643 | T | C | 1 | a0001c0006t0003g0024 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.633+893T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857643 | |||||||
| chr5:56857711 | A | C | 1 | a0002c0004t0001g0082 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.633+961A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857711 | |||||||
| chr5:56857944 | G | T | 4 | a0003c0002t0001g0148 a0003c0002t0001g0165 a0003c0002t0001g0168 others(1): Show |
4 | HG02155.hp2 NA18942.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.633+1194G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857944 | |||||||
| chr5:56857949 | G | A | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.633+1199G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56857949 | |||||||
| chr5:56858020 | G | C | 14 | a0003c0002t0001g0179 a0003c0002t0001g0180 a0003c0002t0001g0181 others(11): Show |
14 | HG00099.hp1 HG01109.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.633+1270G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858020 | |||||||
| chr5:56858072 | A | G | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.633+1322A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858072 | |||||||
| chr5:56858294 | G | C | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.634-1421G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858294 | |||||||
| chr5:56858438 | G | A | 2 | a0001c0001t0002g0275 a0001c0001t0002g0281 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.634-1277G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858438 | |||||||
| chr5:56858548 | G | A | 2 | a0001c0001t0002g0275 a0001c0001t0002g0281 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.634-1167G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858548 | |||||||
| chr5:56858757 | T | A | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.634-958T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858757 | |||||||
| chr5:56858808 | G | A | 20 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(17): Show |
21 | HG00673.hp2 HG02080.hp1 HG02698.hp2 others(18): Show |
intron_variant | MODIFIER | c.634-907G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858808 | |||||||
| chr5:56858817 | T | C | 3 | a0001c0005t0003g0217 a0001c0005t0003g0218 a0001c0005t0003g0221 |
3 | NA18945.hp2 NA18982.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.634-898T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858817 | |||||||
| chr5:56858993 | C | T | 1 | a0001c0006t0003g0024 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.634-722C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56858993 | |||||||
| chr5:56859065 | TA | T | 192 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(189): Show |
213 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.634-631delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 56859065 | ||||||
| chr5:56859065 | TAA | T | 6 | a0001c0001t0002g0274 a0001c0005t0007g0313 a0001c0006t0003g0234 others(3): Show |
7 | HG01243.hp2 HG02809.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.634-632_634-631del others(2): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 56859065 | ||||||
| chr5:56859199 | A | AACAC | 160 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(157): Show |
175 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.634-508_634-505dup others(4): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 56859199 | ||||||
| chr5:56859199 | A | AACACAC | 63 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(60): Show |
71 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.634-510_634-505dup others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 56859199 | ||||||
| chr5:56859422 | T | C | 1 | a0001c0001t0002g0264 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.634-293T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56859422 | |||||||
| chr5:56859455 | T | A | 1 | a0001c0001t0002g0254 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.634-260T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 2/19 | chr5 | 56859455 | |||||||
| chr5:56859924 | A | G | 2 | a0003c0002t0006g0035 a0003c0002t0006g0036 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.834+9A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56859924 | |||||||
| chr5:56860132 | C | T | 1 | a0001c0001t0002g0290 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.834+217C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860132 | |||||||
| chr5:56860385 | A | C | 1 | a0003c0002t0003g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.834+470A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860385 | |||||||
| chr5:56860545 | C | T | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.834+630C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860545 | |||||||
| chr5:56860581 | G | A | 94 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(91): Show |
103 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.834+666G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860581 | |||||||
| chr5:56860583 | T | G | 1 | a0001c0008t0007g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.834+668T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860583 | |||||||
| chr5:56860592 | T | C | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.834+677T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860592 | |||||||
| chr5:56860628 | G | A | 41 | a0002c0004t0001g0001 a0002c0004t0001g0006 a0002c0004t0001g0015 others(38): Show |
48 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.834+713G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860628 | |||||||
| chr5:56860650 | C | T | 1 | a0001c0006t0001g0237 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.834+735C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860650 | |||||||
| chr5:56860818 | A | G | 1 | a0001c0006t0003g0240 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.834+903A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860818 | |||||||
| chr5:56860856 | AAAAAAAA others(1): Show |
A | 50 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(47): Show |
55 | HG00423.hp2 HG00673.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.834+954_834+961del others(8): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56860856 | ||||||
| chr5:56860871 | A | G | 1 | a0003c0002t0003g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.834+956A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860871 | |||||||
| chr5:56860883 | T | G | 2 | a0002c0003t0006g0111 a0002c0003t0006g0114 |
2 | HG02132.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.834+968T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860883 | |||||||
| chr5:56860982 | T | C | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.834+1067T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56860982 | |||||||
| chr5:56860998 | A | AT | 9 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(6): Show |
10 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.834+1084dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56860998 | ||||||
| chr5:56861205 | T | C | 10 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0006g0014 others(7): Show |
11 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.834+1290T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861205 | |||||||
| chr5:56861374 | T | C | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.834+1459T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861374 | |||||||
| chr5:56861551 | C | T | 2 | a0003c0002t0006g0035 a0003c0002t0006g0036 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.834+1636C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861551 | |||||||
| chr5:56861568 | T | TA | 10 | a0002c0003t0001g0049 a0002c0003t0001g0100 a0002c0003t0004g0112 others(7): Show |
10 | HG01361.hp1 HG02071.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.834+1675dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56861568 | ||||||
| chr5:56861568 | TA | T | 9 | a0002c0003t0001g0055 a0002c0003t0001g0088 a0002c0003t0001g0089 others(6): Show |
9 | HG01167.hp2 HG01261.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.834+1675delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56861568 | ||||||
| chr5:56861569 | A | T | 1 | a0001c0001t0002g0290 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.834+1654A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861569 | |||||||
| chr5:56861586 | A | AG | 3 | a0003c0002t0001g0033 a0003c0002t0001g0150 a0003c0002t0001g0182 |
3 | HG02738.hp1 NA18964.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.834+1671_834+1672i others(3): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861586 | |||||||
| chr5:56861587 | A | AG | 47 | a0001c0001t0002g0255 a0001c0001t0002g0269 a0001c0001t0002g0270 others(44): Show |
53 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.834+1672_834+1673i others(3): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861587 | |||||||
| chr5:56861587 | A | G | 18 | a0001c0001t0002g0295 a0003c0002t0001g0033 a0003c0002t0001g0150 others(15): Show |
19 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.834+1672A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861587 | |||||||
| chr5:56861588 | A | AG | 71 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(68): Show |
81 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.834+1673_834+1674i others(3): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861588 | |||||||
| chr5:56861588 | A | AGG | 3 | a0003c0002t0001g0151 a0003c0002t0001g0162 a0003c0002t0001g0173 |
3 | HG00621.hp1 NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.834+1673_834+1674i others(4): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861588 | |||||||
| chr5:56861588 | A | G | 65 | a0001c0001t0002g0255 a0001c0001t0002g0269 a0001c0001t0002g0270 others(62): Show |
72 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.834+1673A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861588 | |||||||
| chr5:56861589 | A | AG | 54 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0213 others(51): Show |
59 | HG00423.hp2 HG00673.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.834+1674_834+1675i others(3): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861589 | |||||||
| chr5:56861589 | A | AGG | 10 | a0001c0001t0002g0253 a0001c0001t0002g0254 a0001c0001t0002g0261 others(7): Show |
10 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.834+1674_834+1675i others(4): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861589 | |||||||
| chr5:56861589 | A | G | 139 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.834+1674A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861589 | |||||||
| chr5:56861590 | A | AAAGG | 10 | a0003c0002t0001g0031 a0003c0002t0003g0039 a0003c0002t0004g0038 others(7): Show |
11 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.834+1675_834+1676i others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861590 | |||||||
| chr5:56861590 | A | AGG | 6 | a0001c0005t0003g0222 a0001c0005t0003g0223 a0001c0006t0003g0235 others(3): Show |
6 | HG01361.hp2 HG02056.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.834+1678_834+1679d others(4): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56861590 | ||||||
| chr5:56861590 | A | G | 204 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(201): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.834+1675A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861590 | |||||||
| chr5:56861710 | GAATCTTA others(17): Show |
G | 1 | a0003c0002t0004g0167 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.834+1796_834+1819d others(26): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861710 | |||||||
| chr5:56861726 | G | C | 1 | a0001c0001t0002g0290 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.834+1811G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861726 | |||||||
| chr5:56861780 | G | A | 4 | a0001c0001t0008g0194 a0001c0001t0008g0195 a0001c0001t0008g0196 others(1): Show |
4 | HG02129.hp1 NA18993.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+1865G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56861780 | |||||||
| chr5:56862086 | TGGGCAGG others(10): Show |
T | 1 | a0009c0016t0002g0280 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.834+2174_834+2190d others(19): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56862086 | ||||||
| chr5:56862108 | G | A | 1 | a0009c0016t0002g0280 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.834+2193G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862108 | |||||||
| chr5:56862110 | T | A | 1 | a0009c0016t0002g0280 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.834+2195T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862110 | |||||||
| chr5:56862124 | T | C | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.834+2209T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862124 | |||||||
| chr5:56862232 | C | G | 1 | a0001c0001t0007g0327 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.834+2317C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862232 | |||||||
| chr5:56862267 | C | T | 1 | a0006c0013t0002g0294 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.834+2352C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862267 | |||||||
| chr5:56862324 | T | A | 1 | a0002c0003t0001g0101 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.834+2409T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862324 | |||||||
| chr5:56862628 | C | T | 2 | a0003c0002t0007g0037 a0003c0002t0011g0207 |
2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.835-2106C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862628 | |||||||
| chr5:56862668 | C | T | 1 | a0003c0002t0001g0146 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.835-2066C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862668 | |||||||
| chr5:56862788 | TA | T | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.835-1945delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862788 | |||||||
| chr5:56862880 | A | G | 4 | a0001c0011t0007g0198 a0001c0011t0007g0199 a0001c0011t0007g0200 others(1): Show |
4 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-1854A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862880 | |||||||
| chr5:56862901 | G | C | 1 | a0002c0003t0001g0060 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.835-1833G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862901 | |||||||
| chr5:56862914 | C | T | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.835-1820C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862914 | |||||||
| chr5:56862944 | A | G | 1 | a0002c0004t0003g0119 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.835-1790A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862944 | |||||||
| chr5:56862953 | T | C | 1 | a0004c0010t0003g0251 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.835-1781T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56862953 | |||||||
| chr5:56863023 | A | G | 1 | a0002c0007t0001g0087 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.835-1711A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863023 | |||||||
| chr5:56863210 | T | A | 1 | a0003c0002t0004g0186 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.835-1524T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863210 | |||||||
| chr5:56863223 | G | A | 2 | a0001c0005t0003g0225 a0001c0005t0003g0226 |
2 | HG03239.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.835-1511G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863223 | |||||||
| chr5:56863344 | A | G | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.835-1390A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863344 | |||||||
| chr5:56863353 | A | C | 1 | a0001c0001t0002g0277 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.835-1381A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863353 | |||||||
| chr5:56863429 | T | A | 1 | a0003c0002t0001g0183 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.835-1305T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863429 | |||||||
| chr5:56863491 | T | G | 1 | a0002c0003t0001g0097 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.835-1243T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863491 | |||||||
| chr5:56863593 | A | G | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.835-1141A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863593 | |||||||
| chr5:56863682 | C | T | 1 | a0003c0002t0001g0183 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.835-1052C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863682 | |||||||
| chr5:56863751 | T | C | 148 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(145): Show |
162 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.835-983T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863751 | |||||||
| chr5:56863786 | A | G | 20 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(17): Show |
21 | HG00673.hp2 HG02080.hp1 HG02698.hp2 others(18): Show |
intron_variant | MODIFIER | c.835-948A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863786 | |||||||
| chr5:56863995 | C | T | 1 | a0003c0002t0006g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.835-739C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56863995 | |||||||
| chr5:56864055 | G | A | 21 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0028 others(18): Show |
27 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.835-679G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864055 | |||||||
| chr5:56864072 | A | G | 2 | a0001c0001t0008g0307 a0001c0001t0010g0306 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.835-662A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864072 | |||||||
| chr5:56864113 | A | G | 1 | a0003c0002t0001g0178 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.835-621A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864113 | |||||||
| chr5:56864159 | G | A | 1 | a0001c0005t0004g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.835-575G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864159 | |||||||
| chr5:56864325 | G | T | 1 | a0002c0004t0004g0103 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.835-409G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864325 | |||||||
| chr5:56864377 | TC | T | 4 | a0002c0003t0001g0115 a0002c0003t0001g0118 a0002c0003t0001g0121 others(1): Show |
4 | HG02040.hp1 HG02071.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.835-356delC | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864377 | |||||||
| chr5:56864378 | C | T | 1 | a0002c0003t0001g0116 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.835-356C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864378 | |||||||
| chr5:56864378 | CT | C | 210 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(207): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.835-339delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56864378 | ||||||
| chr5:56864378 | CTT | C | 6 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(3): Show |
6 | HG00735.hp2 HG01168.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.835-340_835-339del others(2): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56864378 | ||||||
| chr5:56864446 | C | T | 1 | a0001c0001t0011g0320 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.835-288C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | chr5 | 56864446 | |||||||
| chr5:56864714 | T | TA | 13 | a0001c0005t0007g0313 a0001c0005t0007g0314 a0001c0005t0007g0315 others(10): Show |
14 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.835-11dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 56864714 | ||||||
| chr5:56865520 | T | C | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+64T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 5/19 | chr5 | 56865520 | |||||||
| chr5:56866148 | C | T | 81 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(78): Show |
89 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1301+171C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56866148 | |||||||
| chr5:56866204 | G | A | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1301+227G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56866204 | |||||||
| chr5:56866231 | A | G | 2 | a0003c0002t0001g0189 a0003c0002t0001g0190 |
2 | HG00099.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1301+254A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56866231 | |||||||
| chr5:56866323 | G | A | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1301+346G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56866323 | |||||||
| chr5:56866419 | GTGTA | G | 4 | a0005c0012t0008g0057 a0005c0012t0008g0059 a0005c0012t0010g0058 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301+454_1301+457d others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 56866419 | ||||||
| chr5:56866439 | A | C | 1 | a0001c0005t0004g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1301+462A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56866439 | |||||||
| chr5:56866463 | A | T | 1 | a0001c0001t0002g0277 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1301+486A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56866463 | |||||||
| chr5:56867014 | T | C | 2 | a0003c0002t0006g0035 a0003c0002t0006g0036 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1301+1037T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867014 | |||||||
| chr5:56867150 | A | G | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301+1173A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867150 | |||||||
| chr5:56867224 | C | T | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1301+1247C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867224 | |||||||
| chr5:56867246 | T | A | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1301+1269T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867246 | |||||||
| chr5:56867333 | G | A | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1301+1356G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867333 | |||||||
| chr5:56867367 | A | G | 1 | a0002c0003t0001g0060 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1301+1390A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867367 | |||||||
| chr5:56867423 | TA | T | 21 | a0001c0001t0002g0025 a0001c0001t0002g0255 a0001c0001t0002g0263 others(18): Show |
22 | HG00438.hp1 HG01175.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1301+1447delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867423 | |||||||
| chr5:56867428 | C | A | 93 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(90): Show |
102 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1301+1451C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867428 | |||||||
| chr5:56867468 | A | G | 1 | a0002c0004t0001g0065 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1301+1491A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867468 | |||||||
| chr5:56867482 | G | A | 2 | a0003c0002t0006g0035 a0003c0002t0006g0036 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1301+1505G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867482 | |||||||
| chr5:56867573 | T | C | 1 | a0003c0002t0007g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1301+1596T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867573 | |||||||
| chr5:56867643 | A | G | 36 | a0002c0003t0001g0002 a0002c0003t0001g0017 a0002c0003t0001g0050 others(33): Show |
41 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1301+1666A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867643 | |||||||
| chr5:56867960 | G | A | 81 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(78): Show |
89 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1301+1983G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867960 | |||||||
| chr5:56867986 | A | G | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1301+2009A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56867986 | |||||||
| chr5:56868026 | G | A | 8 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0006g0014 others(5): Show |
9 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1301+2049G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868026 | |||||||
| chr5:56868251 | G | C | 4 | a0003c0002t0001g0145 a0003c0002t0001g0146 a0003c0002t0001g0147 others(1): Show |
4 | HG03669.hp1 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301+2274G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868251 | |||||||
| chr5:56868325 | T | TAAAAAAA others(312): Show |
1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1301+2361_1301+236 others(323): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 56868325 | ||||||
| chr5:56868325 | TA | T | 3 | a0002c0003t0001g0017 a0002c0003t0006g0017 a0002c0003t0006g0018 |
4 | HG00423.hp1 NA18612.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301+2356delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 56868325 | ||||||
| chr5:56868396 | C | T | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1301+2419C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868396 | |||||||
| chr5:56868446 | G | A | 6 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0213 others(3): Show |
7 | HG01109.hp1 HG01243.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1301+2469G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868446 | |||||||
| chr5:56868530 | G | A | 1 | a0003c0002t0001g0151 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1301+2553G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868530 | |||||||
| chr5:56868560 | A | G | 2 | a0001c0001t0008g0196 a0001c0001t0008g0197 |
2 | NA18993.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1301+2583A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868560 | |||||||
| chr5:56868605 | C | T | 1 | a0001c0008t0007g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1301+2628C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868605 | |||||||
| chr5:56868631 | G | A | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1301+2654G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868631 | |||||||
| chr5:56868777 | T | A | 2 | a0001c0001t0002g0012 a0001c0001t0002g0284 |
4 | HG01346.hp2 HG01952.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301+2800T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868777 | |||||||
| chr5:56868817 | G | T | 2 | a0001c0001t0002g0260 a0001c0001t0002g0282 |
2 | HG01256.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1301+2840G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868817 | |||||||
| chr5:56868858 | C | T | 1 | a0001c0001t0002g0266 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1301+2881C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868858 | |||||||
| chr5:56868877 | G | C | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1301+2900G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56868877 | |||||||
| chr5:56869086 | C | CA | 11 | a0001c0006t0003g0243 a0003c0002t0001g0031 a0003c0002t0001g0032 others(8): Show |
12 | HG01433.hp1 HG01891.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1302-2812dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 56869086 | ||||||
| chr5:56869097 | A | G | 1 | a0003c0002t0001g0160 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1302-2813A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869097 | |||||||
| chr5:56869116 | A | G | 94 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(91): Show |
103 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1302-2794A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869116 | |||||||
| chr5:56869189 | T | C | 10 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0006g0014 others(7): Show |
11 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302-2721T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869189 | |||||||
| chr5:56869230 | C | T | 4 | a0001c0001t0002g0254 a0001c0005t0003g0217 a0001c0005t0003g0218 others(1): Show |
4 | HG02055.hp1 NA18945.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302-2680C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869230 | |||||||
| chr5:56869370 | A | G | 1 | a0003c0002t0001g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1302-2540A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869370 | |||||||
| chr5:56869427 | A | G | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1302-2483A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869427 | |||||||
| chr5:56869487 | CA | C | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1302-2415delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 56869487 | ||||||
| chr5:56869686 | T | C | 1 | a0001c0001t0009g0030 | 2 | HG02572.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1302-2224T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869686 | |||||||
| chr5:56869928 | C | T | 9 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(6): Show |
10 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302-1982C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56869928 | |||||||
| chr5:56870087 | A | G | 42 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(39): Show |
46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.1302-1823A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870087 | |||||||
| chr5:56870187 | A | G | 4 | a0001c0001t0002g0210 a0001c0001t0002g0254 a0001c0001t0002g0274 others(1): Show |
4 | HG02055.hp1 HG02451.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302-1723A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870187 | |||||||
| chr5:56870201 | A | G | 41 | a0002c0004t0001g0001 a0002c0004t0001g0006 a0002c0004t0001g0015 others(38): Show |
48 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1302-1709A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870201 | |||||||
| chr5:56870243 | G | A | 6 | a0003c0002t0006g0014 a0003c0002t0006g0040 a0003c0002t0006g0041 others(3): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302-1667G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870243 | |||||||
| chr5:56870277 | G | A | 5 | a0003c0002t0001g0193 a0005c0012t0008g0057 a0005c0012t0008g0059 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302-1633G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870277 | |||||||
| chr5:56870361 | A | G | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1302-1549A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870361 | |||||||
| chr5:56870367 | C | T | 63 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(60): Show |
71 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1302-1543C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870367 | |||||||
| chr5:56870368 | G | A | 21 | a0001c0001t0002g0025 a0001c0001t0002g0255 a0001c0001t0002g0263 others(18): Show |
22 | HG00438.hp1 HG01175.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1302-1542G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870368 | |||||||
| chr5:56870795 | G | A | 1 | a0001c0001t0009g0326 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1302-1115G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56870795 | |||||||
| chr5:56871005 | A | G | 1 | a0003c0002t0001g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1302-905A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 6/19 | chr5 | 56871005 | |||||||
| chr5:56872160 | A | G | 6 | a0001c0001t0002g0262 a0001c0001t0002g0296 a0001c0001t0002g0297 others(3): Show |
6 | HG00735.hp2 HG01074.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1423+129A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 7/19 | chr5 | 56872160 | |||||||
| chr5:56872161 | A | G | 1 | a0002c0004t0001g0078 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1423+130A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 7/19 | chr5 | 56872161 | |||||||
| chr5:56872242 | G | A | 4 | a0001c0011t0007g0198 a0001c0011t0007g0199 a0001c0011t0007g0200 others(1): Show |
4 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1423+211G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 7/19 | chr5 | 56872242 | |||||||
| chr5:56872353 | A | G | 1 | a0001c0001t0002g0299 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1424-288A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 7/19 | chr5 | 56872353 | |||||||
| chr5:56872744 | G | A | 1 | a0003c0002t0003g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1505+22G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 8/19 | chr5 | 56872744 | |||||||
| chr5:56873756 | C | T | 1 | a0003c0002t0001g0159 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1686+751C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56873756 | |||||||
| chr5:56873864 | TA | T | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1686+860delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56873864 | |||||||
| chr5:56873874 | A | G | 1 | a0002c0003t0016g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1686+869A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56873874 | |||||||
| chr5:56874095 | C | G | 1 | a0002c0004t0001g0104 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1687-937C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874095 | |||||||
| chr5:56874110 | A | C | 1 | a0002c0004t0001g0104 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1687-922A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874110 | |||||||
| chr5:56874229 | T | G | 5 | a0001c0005t0007g0313 a0001c0005t0007g0314 a0001c0005t0007g0315 others(2): Show |
5 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1687-803T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874229 | |||||||
| chr5:56874246 | T | G | 1 | a0003c0002t0007g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1687-786T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874246 | |||||||
| chr5:56874376 | G | A | 2 | a0002c0004t0001g0068 a0002c0004t0001g0084 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1687-656G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874376 | |||||||
| chr5:56874473 | C | T | 1 | a0003c0002t0001g0158 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1687-559C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874473 | |||||||
| chr5:56874583 | A | T | 1 | a0002c0003t0001g0108 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1687-449A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874583 | |||||||
| chr5:56874648 | A | G | 6 | a0003c0002t0006g0014 a0003c0002t0006g0040 a0003c0002t0006g0041 others(3): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1687-384A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874648 | |||||||
| chr5:56874688 | A | G | 2 | a0001c0006t0003g0246 a0001c0006t0003g0247 |
2 | NA18956.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1687-344A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874688 | |||||||
| chr5:56874931 | G | A | 4 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(1): Show |
4 | HG00735.hp2 HG01516.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1687-101G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874931 | |||||||
| chr5:56874986 | C | G | 43 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(40): Show |
47 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.1687-46C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 9/19 | chr5 | 56874986 | |||||||
| chr5:56875534 | T | C | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1965+224T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56875534 | |||||||
| chr5:56875564 | G | T | 36 | a0002c0003t0001g0002 a0002c0003t0001g0017 a0002c0003t0001g0050 others(33): Show |
41 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1965+254G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56875564 | |||||||
| chr5:56875694 | T | TAAAAC | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1965+401_1965+405d others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr5 | 56875694 | ||||||
| chr5:56876148 | C | T | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1965+838C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876148 | |||||||
| chr5:56876174 | G | C | 42 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(39): Show |
46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.1965+864G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876174 | |||||||
| chr5:56876359 | T | C | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1965+1049T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876359 | |||||||
| chr5:56876377 | G | C | 4 | a0002c0004t0001g0104 a0002c0004t0001g0105 a0002c0004t0001g0106 others(1): Show |
4 | HG00621.hp2 NA18947.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1965+1067G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876377 | |||||||
| chr5:56876447 | G | A | 4 | a0003c0002t0006g0040 a0003c0002t0006g0042 a0003c0002t0006g0043 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1965+1137G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876447 | |||||||
| chr5:56876475 | G | C | 1 | a0001c0001t0002g0287 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1965+1165G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876475 | |||||||
| chr5:56876760 | T | G | 4 | a0001c0011t0007g0198 a0001c0011t0007g0199 a0001c0011t0007g0200 others(1): Show |
4 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1965+1450T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876760 | |||||||
| chr5:56876819 | T | C | 94 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(91): Show |
103 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1965+1509T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876819 | |||||||
| chr5:56876874 | C | T | 1 | a0001c0006t0003g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1965+1564C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876874 | |||||||
| chr5:56876937 | G | T | 4 | a0005c0012t0008g0057 a0005c0012t0008g0059 a0005c0012t0010g0058 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1965+1627G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876937 | |||||||
| chr5:56876951 | G | A | 160 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(157): Show |
175 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.1965+1641G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56876951 | |||||||
| chr5:56877119 | C | T | 1 | a0003c0002t0004g0186 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1965+1809C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877119 | |||||||
| chr5:56877343 | G | A | 1 | a0001c0011t0007g0200 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1966-1637G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877343 | |||||||
| chr5:56877411 | C | T | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1966-1569C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877411 | |||||||
| chr5:56877413 | A | C | 1 | a0001c0001t0008g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1966-1567A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877413 | |||||||
| chr5:56877479 | T | G | 1 | a0001c0005t0007g0314 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1966-1501T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877479 | |||||||
| chr5:56877489 | T | A | 1 | a0001c0001t0002g0254 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1966-1491T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877489 | |||||||
| chr5:56877519 | AAT | A | 3 | a0001c0001t0002g0311 a0003c0002t0001g0179 a0003c0002t0001g0180 |
3 | HG04115.hp2 HG04204.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1966-1460_1966-145 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877519 | |||||||
| chr5:56877520 | AT | A | 45 | a0001c0001t0002g0277 a0001c0001t0002g0286 a0001c0005t0001g0227 others(42): Show |
49 | HG00423.hp2 HG00673.hp2 HG01169.hp1 others(46): Show |
intron_variant | MODIFIER | c.1966-1443delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr5 | 56877520 | ||||||
| chr5:56877520 | ATT | A | 176 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(173): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1966-1444_1966-144 others(6): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr5 | 56877520 | ||||||
| chr5:56877627 | A | G | 1 | a0002c0003t0001g0115 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1966-1353A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56877627 | |||||||
| chr5:56878083 | A | G | 5 | a0001c0001t0008g0209 a0005c0012t0008g0057 a0005c0012t0008g0059 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1966-897A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878083 | |||||||
| chr5:56878107 | G | A | 1 | a0003c0002t0001g0182 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1966-873G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878107 | |||||||
| chr5:56878169 | A | G | 1 | a0001c0001t0002g0263 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1966-811A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878169 | |||||||
| chr5:56878356 | C | T | 3 | a0001c0001t0002g0206 a0001c0001t0002g0259 a0001c0001t0002g0302 |
3 | HG00639.hp2 HG01175.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1966-624C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878356 | |||||||
| chr5:56878382 | A | G | 1 | a0003c0002t0003g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1966-598A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878382 | |||||||
| chr5:56878416 | G | A | 1 | a0001c0005t0007g0315 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1966-564G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878416 | |||||||
| chr5:56878618 | C | T | 1 | a0001c0006t0001g0237 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1966-362C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878618 | |||||||
| chr5:56878625 | A | G | 17 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0028 others(14): Show |
23 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1966-355A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878625 | |||||||
| chr5:56878920 | G | A | 1 | a0002c0004t0001g0065 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1966-60G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 10/19 | chr5 | 56878920 | |||||||
| chr5:56879395 | G | A | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2087+294G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879395 | |||||||
| chr5:56879399 | A | G | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.2087+298A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879399 | |||||||
| chr5:56879549 | C | CACTGAAT | 9 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(6): Show |
10 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2087+448_2087+449i others(9): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879549 | |||||||
| chr5:56879552 | A | T | 9 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(6): Show |
10 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2087+451A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879552 | |||||||
| chr5:56879557 | A | G | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2087+456A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879557 | |||||||
| chr5:56879565 | C | CA | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(83): Show |
94 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.2087+470dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr5 | 56879565 | ||||||
| chr5:56879614 | C | G | 6 | a0003c0002t0006g0014 a0003c0002t0006g0040 a0003c0002t0006g0041 others(3): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2087+513C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879614 | |||||||
| chr5:56879739 | C | G | 81 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(78): Show |
89 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.2087+638C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879739 | |||||||
| chr5:56879857 | A | G | 2 | a0001c0008t0007g0204 a0001c0008t0011g0203 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2087+756A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879857 | |||||||
| chr5:56879873 | C | T | 1 | a0002c0003t0006g0056 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2087+772C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879873 | |||||||
| chr5:56879935 | A | G | 1 | a0001c0006t0003g0243 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2088-776A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56879935 | |||||||
| chr5:56880046 | T | C | 3 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0213 |
3 | HG01109.hp1 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2088-665T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56880046 | |||||||
| chr5:56880144 | T | A | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.2088-567T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56880144 | |||||||
| chr5:56880163 | A | G | 1 | a0001c0006t0003g0243 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2088-548A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56880163 | |||||||
| chr5:56880479 | T | C | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2088-232T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56880479 | |||||||
| chr5:56880619 | C | T | 42 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(39): Show |
46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.2088-92C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56880619 | |||||||
| chr5:56880664 | G | T | 1 | a0002c0003t0016g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2088-47G>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56880664 | |||||||
| chr5:56880667 | T | G | 1 | a0001c0001t0010g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2088-44T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 11/19 | chr5 | 56880667 | |||||||
| chr5:56880815 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2179+13C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 12/19 | chr5 | 56880815 | |||||||
| chr5:56880871 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2179+69C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 12/19 | chr5 | 56880871 | |||||||
| chr5:56881321 | A | G | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2369+49A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 13/19 | chr5 | 56881321 | |||||||
| chr5:56881367 | A | T | 1 | a0001c0001t0002g0278 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2369+95A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 13/19 | chr5 | 56881367 | |||||||
| chr5:56881485 | G | C | 1 | a0003c0009t0001g0029 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2370-85G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 13/19 | chr5 | 56881485 | |||||||
| chr5:56881521 | T | G | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2370-49T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 13/19 | chr5 | 56881521 | |||||||
| chr5:56881542 | T | C | 1 | a0002c0004t0001g0077 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2370-28T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 13/19 | chr5 | 56881542 | |||||||
| chr5:56882891 | T | C | 2 | a0001c0001t0002g0260 a0001c0001t0002g0282 |
2 | HG01256.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3666+25T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/19 | chr5 | 56882891 | |||||||
| chr5:56883001 | C | G | 8 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(5): Show |
9 | HG01081.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3666+135C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/19 | chr5 | 56883001 | |||||||
| chr5:56883034 | T | G | 1 | a0001c0008t0011g0203 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3666+168T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/19 | chr5 | 56883034 | |||||||
| chr5:56883277 | A | G | 1 | a0002c0004t0004g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3667-250A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/19 | chr5 | 56883277 | |||||||
| chr5:56883385 | C | T | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.3667-142C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/19 | chr5 | 56883385 | |||||||
| chr5:56883486 | C | G | 1 | a0004c0010t0003g0250 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3667-41C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/19 | chr5 | 56883486 | |||||||
| chr5:56883514 | G | A | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.3667-13G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 14/19 | chr5 | 56883514 | |||||||
| chr5:56883760 | T | C | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.3819+81T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56883760 | |||||||
| chr5:56883812 | T | C | 1 | a0003c0002t0011g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3819+133T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56883812 | |||||||
| chr5:56883916 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3819+237A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56883916 | |||||||
| chr5:56884146 | C | A | 3 | a0001c0001t0002g0206 a0001c0001t0002g0259 a0001c0001t0002g0302 |
3 | HG00639.hp2 HG01175.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3819+467C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56884146 | |||||||
| chr5:56884146 | C | CA | 4 | a0001c0001t0017g0305 a0001c0006t0001g0237 a0001c0006t0003g0024 others(1): Show |
5 | HG01261.hp1 HG01361.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3819+476dupA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr5 | 56884146 | ||||||
| chr5:56884207 | C | A | 1 | a0001c0001t0002g0262 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3820-457C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56884207 | |||||||
| chr5:56884284 | GTGCGGTG others(6): Show |
G | 1 | a0001c0001t0002g0302 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3820-377_3820-365d others(15): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr5 | 56884284 | ||||||
| chr5:56884285 | T | G | 222 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(219): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.3820-379T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56884285 | |||||||
| chr5:56884298 | T | G | 1 | a0001c0001t0002g0302 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3820-366T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56884298 | |||||||
| chr5:56884469 | T | C | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3820-195T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56884469 | |||||||
| chr5:56884653 | A | G | 63 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(60): Show |
71 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.3820-11A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 15/19 | chr5 | 56884653 | |||||||
| chr5:56884954 | A | G | 4 | a0002c0003t0001g0060 a0002c0003t0001g0062 a0002c0003t0001g0108 others(1): Show |
4 | HG00642.hp1 HG01346.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.3982+128A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 16/19 | chr5 | 56884954 | |||||||
| chr5:56885090 | A | G | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.3982+264A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 16/19 | chr5 | 56885090 | |||||||
| chr5:56885281 | T | C | 1 | a0003c0002t0001g0031 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3982+455T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 16/19 | chr5 | 56885281 | |||||||
| chr5:56885388 | GTTC | G | 221 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.3983-541_3983-539d others(5): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr5 | 56885388 | ||||||
| chr5:56885542 | T | G | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.3983-390T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 16/19 | chr5 | 56885542 | |||||||
| chr5:56885604 | T | G | 13 | a0001c0005t0007g0313 a0001c0005t0007g0314 a0001c0005t0007g0315 others(10): Show |
14 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.3983-328T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 16/19 | chr5 | 56885604 | |||||||
| chr5:56886096 | A | G | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4114+33A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886096 | |||||||
| chr5:56886105 | T | G | 1 | a0001c0005t0007g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4114+42T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886105 | |||||||
| chr5:56886328 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4114+265C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886328 | |||||||
| chr5:56886529 | A | G | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.4114+466A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886529 | |||||||
| chr5:56886585 | A | T | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4114+522A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886585 | |||||||
| chr5:56886642 | A | G | 1 | a0002c0004t0003g0119 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4114+579A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886642 | |||||||
| chr5:56886762 | C | T | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.4115-616C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886762 | |||||||
| chr5:56886847 | T | C | 13 | a0001c0005t0007g0313 a0001c0005t0007g0314 a0001c0005t0007g0315 others(10): Show |
14 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.4115-531T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56886847 | |||||||
| chr5:56887005 | C | T | 1 | a0002c0004t0004g0075 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.4115-373C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56887005 | |||||||
| chr5:56887046 | A | G | 1 | a0001c0001t0009g0323 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4115-332A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56887046 | |||||||
| chr5:56887186 | G | A | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4115-192G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 17/19 | chr5 | 56887186 | |||||||
| chr5:56887578 | A | G | 1 | a0001c0001t0002g0309 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4257+58A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56887578 | |||||||
| chr5:56887715 | C | T | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.4257+195C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56887715 | |||||||
| chr5:56887739 | G | A | 1 | a0002c0003t0001g0053 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4257+219G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56887739 | |||||||
| chr5:56887810 | G | C | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.4257+290G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56887810 | |||||||
| chr5:56887898 | T | C | 1 | a0001c0006t0004g0245 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4258-328T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56887898 | |||||||
| chr5:56887916 | T | G | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.4258-310T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56887916 | |||||||
| chr5:56887970 | C | T | 1 | a0002c0003t0001g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4258-256C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56887970 | |||||||
| chr5:56888102 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4258-124G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56888102 | |||||||
| chr5:56888114 | C | G | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.4258-112C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 18/19 | chr5 | 56888114 | |||||||
| chr5:56888617 | T | C | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.4389+260T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56888617 | |||||||
| chr5:56888783 | C | T | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.4389+426C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56888783 | |||||||
| chr5:56888793 | G | A | 5 | a0001c0005t0007g0313 a0001c0005t0007g0314 a0001c0005t0007g0315 others(2): Show |
5 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4389+436G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56888793 | |||||||
| chr5:56888986 | T | G | 1 | a0001c0001t0002g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4389+629T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56888986 | |||||||
| chr5:56889099 | G | C | 42 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(39): Show |
46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.4389+742G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889099 | |||||||
| chr5:56889175 | G | A | 1 | a0012c0019t0004g0070 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4389+818G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889175 | |||||||
| chr5:56889201 | C | T | 2 | a0003c0002t0007g0037 a0003c0002t0011g0207 |
2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4389+844C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889201 | |||||||
| chr5:56889210 | C | T | 1 | a0001c0001t0002g0289 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4389+853C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889210 | |||||||
| chr5:56889300 | C | CT | 59 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(56): Show |
65 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.4389+944dupT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr5 | 56889300 | ||||||
| chr5:56889316 | G | A | 104 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(101): Show |
114 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.4389+959G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889316 | |||||||
| chr5:56889334 | A | G | 1 | a0001c0001t0011g0320 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4389+977A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889334 | |||||||
| chr5:56889454 | T | A | 223 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.4389+1097T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889454 | |||||||
| chr5:56889489 | A | G | 13 | a0001c0005t0007g0313 a0001c0005t0007g0314 a0001c0005t0007g0315 others(10): Show |
14 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.4389+1132A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889489 | |||||||
| chr5:56889969 | G | A | 1 | a0001c0001t0002g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4389+1612G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889969 | |||||||
| chr5:56889978 | G | A | 4 | a0002c0004t0001g0104 a0002c0004t0001g0105 a0002c0004t0001g0106 others(1): Show |
4 | HG00621.hp2 NA18947.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.4389+1621G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56889978 | |||||||
| chr5:56890035 | A | T | 4 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(1): Show |
5 | HG02809.hp1 HG03225.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.4389+1678A>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890035 | |||||||
| chr5:56890162 | C | T | 2 | a0003c0002t0001g0150 a0003c0002t0001g0163 |
2 | NA18992.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.4389+1805C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890162 | |||||||
| chr5:56890212 | C | T | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.4389+1855C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890212 | |||||||
| chr5:56890435 | C | G | 2 | a0002c0003t0005g0131 a0002c0003t0005g0132 |
2 | HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.4389+2078C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890435 | |||||||
| chr5:56890492 | G | A | 1 | a0002c0004t0001g0105 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4389+2135G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890492 | |||||||
| chr5:56890612 | G | A | 42 | a0001c0005t0001g0227 a0001c0005t0003g0023 a0001c0005t0003g0214 others(39): Show |
46 | HG00423.hp2 HG00673.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.4389+2255G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890612 | |||||||
| chr5:56890662 | C | T | 1 | a0002c0007t0001g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4389+2305C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890662 | |||||||
| chr5:56890819 | A | G | 13 | a0001c0005t0007g0313 a0001c0005t0007g0314 a0001c0005t0007g0315 others(10): Show |
14 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.4389+2462A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890819 | |||||||
| chr5:56890881 | C | A | 1 | a0001c0001t0002g0285 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4389+2524C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56890881 | |||||||
| chr5:56891036 | C | T | 2 | a0003c0002t0007g0037 a0003c0002t0011g0207 |
2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4390-2495C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891036 | |||||||
| chr5:56891148 | A | AC | 18 | a0001c0011t0007g0198 a0001c0011t0007g0199 a0001c0011t0007g0201 others(15): Show |
19 | HG00642.hp1 HG01081.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.4390-2371dupC | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr5 | 56891148 | ||||||
| chr5:56891148 | A | C | 1 | a0002c0003t0005g0008 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4390-2383A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891148 | |||||||
| chr5:56891148 | AC | A | 47 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0028 others(44): Show |
60 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.4390-2371delC | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr5 | 56891148 | ||||||
| chr5:56891148 | ACCC | A | 186 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 others(183): Show |
201 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.4390-2373_4390-237 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr5 | 56891148 | ||||||
| chr5:56891151 | C | A | 1 | a0001c0001t0002g0286 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4390-2380C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891151 | |||||||
| chr5:56891153 | C | A | 3 | a0001c0001t0011g0320 a0003c0002t0003g0039 a0003c0002t0004g0038 |
3 | HG01891.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4390-2378C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891153 | |||||||
| chr5:56891157 | C | A | 79 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0028 others(76): Show |
93 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.4390-2374C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891157 | |||||||
| chr5:56891159 | C | A | 140 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(137): Show |
157 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.4390-2372C>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891159 | |||||||
| chr5:56891160 | CA | C | 4 | a0001c0008t0007g0022 a0002c0004t0004g0075 a0002c0004t0004g0103 others(1): Show |
4 | HG03225.hp1 HG03492.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.4390-2370delA | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891160 | |||||||
| chr5:56891160 | CACA | C | 4 | a0001c0005t0007g0313 a0001c0005t0007g0314 a0001c0005t0007g0315 others(1): Show |
4 | HG02451.hp1 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.4390-2370_4390-236 others(7): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891160 | |||||||
| chr5:56891161 | A | C | 15 | a0001c0008t0007g0022 a0001c0008t0007g0202 a0001c0008t0007g0204 others(12): Show |
15 | HG01081.hp2 HG01943.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.4390-2370A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891161 | |||||||
| chr5:56891163 | A | C | 5 | a0001c0005t0007g0317 a0001c0008t0007g0022 a0001c0008t0007g0202 others(2): Show |
6 | HG01884.hp2 HG02809.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.4390-2368A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891163 | |||||||
| chr5:56891248 | G | A | 3 | a0001c0001t0002g0205 a0001c0001t0002g0272 a0001c0001t0008g0292 |
3 | HG00738.hp2 HG01074.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.4390-2283G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891248 | |||||||
| chr5:56891272 | G | A | 1 | a0001c0001t0002g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4390-2259G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891272 | |||||||
| chr5:56891370 | A | G | 1 | a0002c0003t0001g0122 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4390-2161A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891370 | |||||||
| chr5:56891506 | G | A | 1 | a0002c0004t0004g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4390-2025G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891506 | |||||||
| chr5:56891563 | T | C | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.4390-1968T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891563 | |||||||
| chr5:56891749 | A | C | 1 | a0001c0005t0001g0227 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4390-1782A>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891749 | |||||||
| chr5:56891988 | TTTTGGCT others(8): Show |
T | 1 | a0001c0005t0003g0226 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.4390-1542_4390-152 others(19): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56891988 | |||||||
| chr5:56892021 | C | T | 1 | a0002c0003t0016g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4390-1510C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892021 | |||||||
| chr5:56892185 | T | G | 12 | a0003c0002t0001g0031 a0003c0002t0001g0032 a0003c0002t0003g0039 others(9): Show |
13 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.4390-1346T>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892185 | |||||||
| chr5:56892544 | C | G | 60 | a0003c0002t0001g0003 a0003c0002t0001g0010 a0003c0002t0001g0013 others(57): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.4390-987C>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892544 | |||||||
| chr5:56892589 | A | G | 1 | a0001c0001t0002g0277 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4390-942A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892589 | |||||||
| chr5:56892742 | G | C | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.4390-789G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892742 | |||||||
| chr5:56892916 | T | C | 7 | a0003c0002t0001g0013 a0003c0002t0001g0033 a0003c0002t0001g0034 others(4): Show |
8 | HG00558.hp1 HG00597.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.4390-615T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892916 | |||||||
| chr5:56892967 | CT | C | 22 | a0001c0001t0002g0281 a0001c0001t0007g0327 a0001c0001t0009g0030 others(19): Show |
25 | HG00621.hp1 HG01167.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.4390-555delT | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr5 | 56892967 | ||||||
| chr5:56892972 | T | TA | 14 | a0001c0005t0003g0226 a0001c0005t0007g0313 a0001c0005t0007g0314 others(11): Show |
15 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.4390-559_4390-558i others(3): Show |
MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892972 | |||||||
| chr5:56892973 | T | A | 199 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(196): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.4390-558T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892973 | |||||||
| chr5:56892974 | T | A | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.4390-557T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892974 | |||||||
| chr5:56892975 | T | A | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.4390-556T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892975 | |||||||
| chr5:56892976 | T | A | 314 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(311): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.4390-555T>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56892976 | |||||||
| chr5:56893083 | T | C | 2 | a0001c0001t0002g0273 a0001c0001t0002g0288 |
2 | HG00609.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.4390-448T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893083 | |||||||
| chr5:56893100 | T | C | 1 | a0003c0002t0004g0157 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4390-431T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893100 | |||||||
| chr5:56893104 | T | C | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.4390-427T>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893104 | |||||||
| chr5:56893150 | G | A | 220 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0025 others(217): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.4390-381G>A | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893150 | |||||||
| chr5:56893204 | A | G | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.4390-327A>G | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893204 | |||||||
| chr5:56893290 | G | C | 1 | a0002c0003t0001g0091 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4390-241G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893290 | |||||||
| chr5:56893344 | G | C | 3 | a0003c0009t0001g0029 a0003c0009t0004g0318 a0003c0009t0004g0319 |
4 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4390-187G>C | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893344 | |||||||
| chr5:56893383 | C | T | 6 | a0003c0002t0006g0014 a0003c0002t0006g0040 a0003c0002t0006g0041 others(3): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.4390-148C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893383 | |||||||
| chr5:56893423 | C | T | 10 | a0001c0001t0007g0327 a0001c0001t0009g0030 a0001c0001t0009g0321 others(7): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.4390-108C>T | MAP3K1 | ENSG00000095015.6 | transcript | ENST00000399503.4 | protein_coding | 19/19 | chr5 | 56893423 |