Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5605 |
| ensemblid | ENSG00000126934.15 |
| hgncid | 6842 |
| symbol | MAP2K2 |
| name | mitogen-activated protein kinase kinase 2 |
| refseq_nuc | NM_030662.4 |
| refseq_prot | NP_109587.1 |
| ensembl_nuc | ENST00000262948.10 |
| ensembl_prot | ENSP00000262948.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 4090321 |
| end | 4124122 |
| strand | - |
| ver | v1.2 |
| region | chr19:4090321-4124122 |
| region5000 | chr19:4085321-4129122 |
| regionname0 | MAP2K2_chr19_4090321_4124122 |
| regionname5000 | MAP2K2_chr19_4085321_4129122 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 400 | 326 | 83 | 74 | 111 | 10 | 46 | 80 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | MLARR others(395): Show |
chr19 | 4085321 | 4129122 |
| a0002 | 0/0 | 400 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | MLARR others(395): Show |
chr19 | 4085321 | 4129122 |
| a0003 | 0/0 | 400 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | MLARR others(395): Show |
chr19 | 4085321 | 4129122 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1200 | 145 | 49 | 30 | 43 | 2 | 20 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | ATGCT others(1195): Show |
chr19 | 4085321 | 4129122 | ||
| a0001c0002 | 0/0 | 1200 | 114 | 12 | 30 | 56 | 6 | 10 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | ATGCT others(1195): Show |
chr19 | 4085321 | 4129122 | ||
| a0001c0003 | 0/1 | 1200 | 24 | 2 | 6 | 5 | 2 | 8 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | ATGCT others(1195): Show |
chr19 | 4085321 | 4129122 | ||
| a0001c0004 | 0/0 | 1200 | 12 | 12 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | ATGCT others(1195): Show |
chr19 | 4085321 | 4129122 | ||
| a0001c0005 | 0/0 | 1200 | 12 | 2 | 3 | 0 | 0 | 7 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | ATGCT others(1195): Show |
chr19 | 4085321 | 4129122 | ||
| a0001c0006 | 0/0 | 1200 | 11 | 6 | 1 | 4 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | ATGCT others(1195): Show |
chr19 | 4085321 | 4129122 | ||
| a0001c0007 | 0/0 | 1200 | 5 | 0 | 4 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | ATGCT others(1195): Show |
chr19 | 4085321 | 4129122 | ||
| a0001c0009 | 0/0 | 1200 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | ATGCT others(1195): Show |
chr19 | 4085321 | 4129122 | ||
| a0001c0011 | 0/0 | 1200 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | ATGCT others(1195): Show |
chr19 | 4085321 | 4129122 | ||
| a0002c0008 | 0/0 | 1200 | 3 | 0 | 0 | 3 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | ATGCT others(1195): Show |
chr19 | 4085321 | 4129122 | ||
| a0003c0010 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | ATGCT others(1195): Show |
chr19 | 4085321 | 4129122 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1727 | 73 | 20 | 14 | 27 | 2 | 9 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0001t0002 | 0/0 | 1727 | 41 | 1 | 15 | 16 | 0 | 9 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0001t0003 | 0/0 | 1727 | 10 | 9 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0001t0004 | 0/0 | 1727 | 14 | 14 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTT others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0001t0005 | 0/0 | 1727 | 7 | 5 | 0 | 0 | 0 | 2 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0002t0001 | 0/0 | 1727 | 98 | 3 | 27 | 54 | 4 | 10 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0002t0002 | 0/0 | 1727 | 6 | 0 | 3 | 1 | 2 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0002t0003 | 0/0 | 1727 | 6 | 6 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0002t0007 | 0/0 | 1727 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0002t0009 | 0/0 | 1727 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0003t0001 | 0/1 | 1727 | 18 | 1 | 6 | 3 | 2 | 5 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0003t0002 | 0/0 | 1727 | 3 | 0 | 0 | 2 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0003t0005 | 0/0 | 1727 | 3 | 1 | 0 | 0 | 0 | 2 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0004t0001 | 0/0 | 1727 | 8 | 8 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0004t0006 | 0/0 | 1725 | 4 | 4 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1720): Show |
chr19 | 4085321 | 4129122 |
| a0001c0005t0001 | 0/0 | 1727 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0005t0003 | 0/0 | 1727 | 11 | 2 | 3 | 0 | 0 | 6 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0006t0001 | 0/0 | 1727 | 6 | 2 | 0 | 4 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0006t0004 | 0/0 | 1727 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTT others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0006t0007 | 0/0 | 1727 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0006t0008 | 0/0 | 1727 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTT others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0007t0001 | 0/0 | 1727 | 5 | 0 | 4 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0009t0001 | 0/0 | 1727 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0001c0011t0001 | 0/0 | 1727 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0002c0008t0001 | 0/0 | 1727 | 3 | 0 | 0 | 3 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| a0003c0010t0003 | 0/0 | 1727 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | CTCTC others(1722): Show |
chr19 | 4085321 | 4129122 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0001t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0001 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0007g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0002t0009g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0005g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0005g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0003t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0004t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0004t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0004t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0004t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0004t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0004t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0004t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0004t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0005t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0005t0003g0002 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0005t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0005t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0005t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0005t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0005t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0005t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0005t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0006t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0006t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0006t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0006t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0006t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0006t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0006t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0006t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0006t0008g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0006t0008g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0006t0008g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0007t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0007t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0007t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0007t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0007t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0009t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0009t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0001c0011t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0002c0008t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0002c0008t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0002c0008t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| a0003c0010t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0217 | EUR | GBR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0101 | EUR | GBR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | FIN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00408 | hp2 | a0001 | c0006 | t0001 | g0025 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00609 | hp1 | a0002 | c0008 | t0001 | g0225 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00639 | hp1 | a0001 | c0005 | t0003 | g0267 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00733 | hp1 | a0001 | c0003 | t0001 | g0102 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0176 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0098 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0252 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01069 | hp1 | a0001 | c0007 | t0001 | g0234 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01070 | hp1 | a0001 | c0005 | t0003 | g0002 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01071 | hp1 | a0001 | c0005 | t0003 | g0002 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01071 | hp2 | a0001 | c0007 | t0001 | g0235 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0211 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01109 | hp2 | a0001 | c0006 | t0004 | g0297 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0095 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0097 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01175 | hp1 | a0001 | c0007 | t0001 | g0039 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01256 | hp1 | a0001 | c0007 | t0001 | g0248 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0169 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0162 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0228 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0251 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0239 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0262 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0222 | EUR | IBS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0201 | EUR | IBS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0184 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01884 | hp2 | a0001 | c0006 | t0008 | g0314 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0191 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0177 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0226 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0179 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02027 | hp1 | a0001 | c0002 | t0009 | g0282 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0038 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CDX | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02155 | hp2 | a0001 | c0009 | t0001 | g0175 | EAS | CDX | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | CDX | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | CDX | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0313 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02257 | hp2 | a0001 | c0006 | t0001 | g0279 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0223 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0311 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02615 | hp1 | a0001 | c0004 | t0001 | g0197 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02622 | hp1 | a0001 | c0002 | t0007 | g0285 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0076 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0312 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02683 | hp2 | a0001 | c0005 | t0003 | g0268 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0253 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0276 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0128 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0290 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02738 | hp2 | a0001 | c0005 | t0003 | g0042 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02809 | hp1 | a0001 | c0002 | t0007 | g0284 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0292 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02886 | hp2 | a0001 | c0005 | t0003 | g0272 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0304 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02896 | hp2 | a0001 | c0002 | t0003 | g0187 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02897 | hp1 | a0001 | c0004 | t0006 | g0196 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02897 | hp2 | a0001 | c0002 | t0003 | g0185 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0291 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0306 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0309 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03098 | hp1 | a0001 | c0006 | t0008 | g0299 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0301 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0303 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03209 | hp1 | a0001 | c0005 | t0003 | g0269 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0288 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0310 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03225 | hp2 | a0001 | c0004 | t0006 | g0194 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03453 | hp1 | a0001 | c0006 | t0007 | g0295 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0293 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0186 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0157 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03490 | hp2 | a0001 | c0011 | t0001 | g0265 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0158 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03516 | hp1 | a0001 | c0006 | t0008 | g0298 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0192 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03540 | hp1 | a0001 | c0004 | t0006 | g0195 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0305 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0289 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03654 | hp1 | a0001 | c0005 | t0003 | g0072 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0083 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0283 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0037 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03704 | hp1 | a0001 | c0003 | t0005 | g0287 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0216 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0052 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03710 | hp2 | a0001 | c0005 | t0003 | g0002 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03834 | hp2 | a0001 | c0005 | t0003 | g0002 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0071 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0049 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG04115 | hp2 | a0001 | c0003 | t0002 | g0145 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0082 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0204 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG04199 | hp2 | a0001 | c0005 | t0003 | g0266 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0058 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG04204 | hp2 | a0001 | c0003 | t0005 | g0286 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG04228 | hp1 | a0001 | c0005 | t0001 | g0271 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18612 | hp1 | a0001 | c0003 | t0001 | g0028 | EAS | CHB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | CHB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18747 | hp2 | a0001 | c0006 | t0001 | g0023 | EAS | CHB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18906 | hp1 | a0001 | c0003 | t0005 | g0296 | AFR | YRI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18906 | hp2 | a0001 | c0004 | t0001 | g0264 | AFR | YRI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18954 | hp2 | a0001 | c0009 | t0001 | g0200 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18962 | hp1 | a0002 | c0008 | t0001 | g0208 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18970 | hp2 | a0001 | c0003 | t0002 | g0140 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18981 | hp1 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18983 | hp1 | a0001 | c0007 | t0001 | g0019 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0280 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18999 | hp2 | a0001 | c0006 | t0001 | g0024 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19010 | hp1 | a0001 | c0003 | t0002 | g0150 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0067 | AFR | LWK | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19030 | hp2 | a0001 | c0002 | t0007 | g0294 | AFR | LWK | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19059 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19059 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19067 | hp1 | a0001 | c0006 | t0001 | g0022 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19081 | hp2 | a0002 | c0008 | t0001 | g0224 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0183 | AFR | YRI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0193 | AFR | YRI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0096 | AFR | ASW | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | ASW | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0249 | EUR | TSI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0236 | EUR | TSI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0203 | EUR | TSI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | GIH | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0135 | SAS | GIH | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0059 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02486 | hp1 | a0003 | c0010 | t0003 | g0270 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0308 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0263 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03471 | hp1 | a0001 | c0006 | t0001 | g0273 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0300 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0307 | AFR | USA | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | USA | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA20300 | hp1 | a0001 | c0004 | t0006 | g0066 | AFR | USA | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | USA | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0027 | REF | REF | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0031 | REF | REF | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4090639 | G | A | 1 | a0003 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1162C>T | p.Arg388Trp | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 11/11 | 1409/1727 | 1162/1203 | 388/400 | chr19 | 4090639 | |||
| chr19:4099227 | G | A | 1 | a0002 | 3 | HG00609.hp1 NA18962.hp1 NA19081.hp2 |
missense_variant | MODERATE | c.893C>T | p.Pro298Leu | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/11 | 1140/1727 | 893/1203 | 298/400 | chr19 | 4099227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4101064 | G | T | 6 | a0001c0002 a0001c0005 a0001c0007 others(3): Show |
137 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(134): Show |
synonymous_variant | LOW | c.660C>A | p.Ile220Ile | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/11 | 907/1727 | 660/1203 | 220/400 | chr19 | 4101064 | |||
| chr19:4102451 | G | A | 3 | a0001c0003 a0001c0007 a0001c0011 |
29 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(26): Show |
splice_region_variant&synonymous_variant | LOW | c.453C>T | p.Asp151Asp | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/11 | 700/1727 | 453/1203 | 151/400 | chr19 | 4102451 | |||
| chr19:4110554 | C | G | 1 | a0001c0004 | 12 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(9): Show |
synonymous_variant | LOW | c.405G>C | p.Gly135Gly | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/11 | 652/1727 | 405/1203 | 135/400 | chr19 | 4110554 | |||
| chr19:4117431 | G | T | 1 | a0001c0009 | 2 | HG02155.hp2 NA18954.hp2 |
synonymous_variant | LOW | c.291C>A | p.Ile97Ile | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/11 | 538/1727 | 291/1203 | 97/400 | chr19 | 4117431 | |||
| chr19:4117530 | G | A | 4 | a0001c0005 a0001c0006 a0001c0011 others(1): Show |
25 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
synonymous_variant | LOW | c.192C>T | p.Val64Val | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/11 | 439/1727 | 192/1203 | 64/400 | chr19 | 4117530 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4090336 | CCT | C | 1 | a0001c0004t0006 | 4 | HG02897.hp1 HG03225.hp2 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*260_*261delAG | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 11/11 | 260 | chr19 | 4090336 | ||||||
| chr19:4090424 | G | T | 8 | a0001c0001t0003 a0001c0001t0004 a0001c0002t0003 others(5): Show |
47 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*174C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 11/11 | 174 | chr19 | 4090424 | ||||||
| chr19:4090574 | G | A | 3 | a0001c0001t0002 a0001c0002t0002 a0001c0003t0002 |
50 | HG00099.hp1 HG00423.hp2 HG00597.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*24C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 11/11 | 24 | chr19 | 4090574 | ||||||
| chr19:4123982 | G | A | 1 | a0001c0002t0009 | 1 | HG02027.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-107C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/11 | chr19 | 4123982 | |||||||
| chr19:4124081 | C | A | 4 | a0001c0001t0005 a0001c0002t0007 a0001c0003t0005 others(1): Show |
14 | HG02622.hp1 HG02735.hp2 HG02809.hp1 others(11): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-206G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/11 | chr19 | 4124081 | |||||||
| chr19:4124118 | G | A | 3 | a0001c0001t0004 a0001c0006t0004 a0001c0006t0008 |
18 | HG01109.hp2 HG01884.hp2 HG02257.hp1 others(15): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-243C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/11 | chr19 | 4124118 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4090714 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.1093-6T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4090714 | |||||||
| chr19:4090836 | C | T | 1 | a0001c0002t0001g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1093-128G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4090836 | |||||||
| chr19:4090855 | G | A | 1 | a0001c0002t0001g0254 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1093-147C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4090855 | |||||||
| chr19:4090981 | G | A | 3 | a0001c0001t0001g0275 a0001c0006t0001g0279 a0001c0006t0008g0314 |
3 | HG01884.hp2 HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1093-273C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4090981 | |||||||
| chr19:4090994 | C | T | 1 | a0001c0002t0001g0064 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1093-286G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4090994 | |||||||
| chr19:4091293 | G | A | 1 | a0001c0004t0006g0196 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1093-585C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091293 | |||||||
| chr19:4091356 | AT | A | 7 | a0001c0001t0001g0219 a0001c0001t0002g0146 a0001c0001t0005g0291 others(4): Show |
7 | HG01168.hp1 HG01169.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1093-649delA | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091356 | |||||||
| chr19:4091395 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1093-687G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091395 | |||||||
| chr19:4091438 | C | T | 74 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0063 others(71): Show |
78 | HG00099.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1093-730G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091438 | |||||||
| chr19:4091445 | C | T | 1 | a0001c0002t0001g0070 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1093-737G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091445 | |||||||
| chr19:4091446 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1093-738C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091446 | |||||||
| chr19:4091572 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0088 a0001c0001t0001g0089 |
3 | NA18944.hp2 NA18945.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1093-864G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091572 | |||||||
| chr19:4091613 | G | A | 13 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0073 others(10): Show |
14 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1093-905C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091613 | |||||||
| chr19:4091618 | G | A | 7 | a0001c0001t0005g0288 a0001c0001t0005g0289 a0001c0001t0005g0291 others(4): Show |
7 | HG02886.hp1 HG02922.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-910C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091618 | |||||||
| chr19:4091781 | T | C | 8 | a0001c0001t0003g0122 a0001c0004t0001g0192 a0001c0004t0001g0193 others(5): Show |
8 | HG01891.hp1 HG02615.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1093-1073A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091781 | |||||||
| chr19:4092138 | C | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0274 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-1430G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092138 | |||||||
| chr19:4092374 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1093-1666C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092374 | |||||||
| chr19:4092537 | C | A | 2 | a0001c0001t0001g0174 a0001c0004t0001g0264 |
2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1093-1829G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092537 | |||||||
| chr19:4092660 | A | G | 1 | a0001c0002t0001g0250 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1092+1793T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092660 | |||||||
| chr19:4092683 | G | A | 6 | a0001c0001t0001g0174 a0001c0001t0001g0274 a0001c0001t0001g0281 others(3): Show |
6 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092+1770C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092683 | |||||||
| chr19:4092810 | A | G | 77 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0062 others(74): Show |
81 | HG00099.hp1 HG00423.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1092+1643T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092810 | |||||||
| chr19:4092888 | T | C | 2 | a0001c0001t0002g0034 a0001c0001t0002g0045 |
2 | HG02055.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1092+1565A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092888 | |||||||
| chr19:4092925 | C | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0274 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1092+1528G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092925 | |||||||
| chr19:4093128 | G | A | 1 | a0001c0002t0007g0284 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1092+1325C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4093128 | |||||||
| chr19:4093228 | AAAC | A | 8 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0092 others(5): Show |
9 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1092+1222_1092+122 others(7): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4093228 | |||||||
| chr19:4093435 | A | C | 1 | a0001c0004t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1092+1018T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4093435 | |||||||
| chr19:4093499 | T | A | 2 | a0001c0006t0001g0273 a0001c0006t0008g0299 |
2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1092+954A>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4093499 | |||||||
| chr19:4093573 | C | G | 1 | a0001c0002t0001g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1092+880G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4093573 | |||||||
| chr19:4094068 | A | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0063 others(23): Show |
27 | HG01168.hp2 HG01358.hp2 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.1092+385T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094068 | |||||||
| chr19:4094108 | C | G | 1 | a0001c0002t0001g0212 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1092+345G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094108 | |||||||
| chr19:4094112 | G | T | 156 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0061 others(153): Show |
167 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1092+341C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094112 | |||||||
| chr19:4094140 | A | G | 1 | a0001c0001t0003g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1092+313T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094140 | |||||||
| chr19:4094205 | G | A | 1 | a0001c0002t0001g0180 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1092+248C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094205 | |||||||
| chr19:4094270 | C | A | 1 | a0001c0001t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1092+183G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094270 | |||||||
| chr19:4094283 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1092+170A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094283 | |||||||
| chr19:4094326 | C | T | 3 | a0001c0001t0004g0301 a0001c0001t0004g0304 a0001c0001t0004g0305 |
3 | HG02896.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1092+127G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094326 | |||||||
| chr19:4094412 | C | A | 1 | a0001c0004t0006g0196 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1092+41G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094412 | |||||||
| chr19:4094529 | C | T | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1047-31G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094529 | |||||||
| chr19:4094577 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1047-79G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094577 | |||||||
| chr19:4094637 | G | GC | 7 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0274 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1047-140_1047-139i others(3): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094637 | |||||||
| chr19:4094710 | C | A | 1 | a0001c0002t0001g0213 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1047-212G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094710 | |||||||
| chr19:4094762 | G | T | 1 | a0001c0001t0003g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1047-264C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094762 | |||||||
| chr19:4094777 | G | A | 138 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0061 others(135): Show |
149 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1047-279C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094777 | |||||||
| chr19:4094828 | G | A | 4 | a0001c0001t0001g0056 a0001c0001t0003g0057 a0001c0001t0003g0090 others(1): Show |
4 | HG01099.hp2 HG01192.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047-330C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094828 | |||||||
| chr19:4094864 | C | A | 1 | a0001c0002t0002g0280 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1047-366G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094864 | |||||||
| chr19:4094889 | G | A | 2 | a0001c0001t0003g0057 a0001c0001t0003g0091 |
2 | HG01099.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1047-391C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094889 | |||||||
| chr19:4094937 | G | A | 1 | a0001c0006t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1047-439C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094937 | |||||||
| chr19:4095032 | C | A | 1 | a0001c0002t0002g0223 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1046+356G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4095032 | |||||||
| chr19:4095055 | G | A | 1 | a0001c0005t0003g0269 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1046+333C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4095055 | |||||||
| chr19:4095115 | C | T | 1 | a0001c0002t0001g0055 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1046+273G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4095115 | |||||||
| chr19:4095188 | G | A | 2 | a0001c0006t0001g0273 a0001c0006t0008g0299 |
2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1046+200C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4095188 | |||||||
| chr19:4095599 | G | C | 7 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0274 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.985-150C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4095599 | |||||||
| chr19:4095622 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.985-173C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4095622 | |||||||
| chr19:4095657 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.985-208C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4095657 | |||||||
| chr19:4095867 | G | A | 6 | a0001c0001t0001g0174 a0001c0001t0001g0274 a0001c0001t0001g0281 others(3): Show |
6 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.985-418C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4095867 | |||||||
| chr19:4095880 | T | C | 1 | a0001c0002t0001g0069 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.985-431A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4095880 | |||||||
| chr19:4096024 | TG | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0274 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.985-576delC | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096024 | |||||||
| chr19:4096035 | A | G | 7 | a0001c0001t0005g0288 a0001c0001t0005g0289 a0001c0001t0005g0291 others(4): Show |
7 | HG02886.hp1 HG02922.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.985-586T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096035 | |||||||
| chr19:4096052 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.985-603G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096052 | |||||||
| chr19:4096128 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.985-679C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096128 | |||||||
| chr19:4096147 | C | A | 1 | a0001c0002t0001g0253 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.985-698G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096147 | |||||||
| chr19:4096157 | G | A | 6 | a0001c0001t0001g0174 a0001c0001t0001g0274 a0001c0001t0001g0281 others(3): Show |
6 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.985-708C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096157 | |||||||
| chr19:4096189 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.985-740G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096189 | |||||||
| chr19:4096214 | G | A | 110 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0065 others(107): Show |
118 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.985-765C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096214 | |||||||
| chr19:4096306 | G | A | 1 | a0001c0002t0001g0221 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.985-857C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096306 | |||||||
| chr19:4096321 | C | T | 1 | a0001c0006t0008g0299 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.985-872G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096321 | |||||||
| chr19:4096446 | G | A | 2 | a0001c0001t0001g0174 a0001c0004t0001g0264 |
2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.984+833C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096446 | |||||||
| chr19:4096512 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0274 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.984+767C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096512 | |||||||
| chr19:4096514 | G | A | 2 | a0001c0001t0001g0104 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.984+765C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096514 | |||||||
| chr19:4096681 | C | T | 2 | a0001c0001t0002g0034 a0001c0001t0002g0045 |
2 | HG02055.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.984+598G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096681 | |||||||
| chr19:4096781 | C | T | 110 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0065 others(107): Show |
118 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.984+498G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096781 | |||||||
| chr19:4096839 | C | T | 1 | a0001c0002t0001g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.984+440G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096839 | |||||||
| chr19:4096972 | G | A | 6 | a0001c0001t0001g0174 a0001c0001t0001g0274 a0001c0001t0001g0281 others(3): Show |
6 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.984+307C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096972 | |||||||
| chr19:4097027 | C | CA | 19 | a0001c0001t0001g0050 a0001c0001t0001g0074 a0001c0001t0001g0084 others(16): Show |
19 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.984+251dupT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4097027 | |||||||
| chr19:4097027 | CA | C | 174 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0061 others(171): Show |
185 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.984+251delT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4097027 | |||||||
| chr19:4097027 | CAA | C | 19 | a0001c0001t0001g0056 a0001c0001t0001g0219 a0001c0001t0002g0146 others(16): Show |
22 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.984+250_984+251del others(2): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4097027 | |||||||
| chr19:4097205 | T | TA | 211 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0036 others(208): Show |
226 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.984+73dupT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4097205 | |||||||
| chr19:4097205 | T | TAA | 17 | a0001c0001t0001g0085 a0001c0001t0001g0275 a0001c0001t0002g0047 others(14): Show |
17 | HG00741.hp1 HG00741.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.984+72_984+73dupTT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4097205 | |||||||
| chr19:4097367 | T | C | 8 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(5): Show |
8 | HG00639.hp2 HG02071.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.920-24A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4097367 | |||||||
| chr19:4097705 | C | A | 19 | a0001c0001t0003g0087 a0001c0001t0003g0172 a0001c0001t0003g0277 others(16): Show |
19 | HG01109.hp2 HG02109.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.920-362G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4097705 | |||||||
| chr19:4097867 | GTGGGCTG others(6): Show |
G | 134 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0061 others(131): Show |
145 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.920-537_920-525del others(13): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4097867 | |||||||
| chr19:4097868 | T | C | 7 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0274 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-525A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4097868 | |||||||
| chr19:4098007 | G | A | 1 | a0001c0002t0001g0226 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.920-664C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098007 | |||||||
| chr19:4098102 | A | C | 1 | a0001c0001t0002g0051 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.920-759T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098102 | |||||||
| chr19:4098146 | AT | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0274 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-804delA | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098146 | |||||||
| chr19:4098284 | A | T | 1 | a0001c0003t0002g0145 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.919+917T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098284 | |||||||
| chr19:4098478 | G | C | 4 | a0001c0001t0001g0056 a0001c0001t0003g0057 a0001c0001t0003g0090 others(1): Show |
4 | HG01099.hp2 HG01192.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+723C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098478 | |||||||
| chr19:4098642 | G | A | 8 | a0001c0002t0001g0076 a0001c0004t0001g0192 a0001c0004t0001g0193 others(5): Show |
8 | HG02615.hp1 HG02647.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+559C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098642 | |||||||
| chr19:4098663 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.919+538A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098663 | |||||||
| chr19:4098778 | A | G | 254 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0021 others(251): Show |
269 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.919+423T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098778 | |||||||
| chr19:4098799 | T | C | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.919+402A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098799 | |||||||
| chr19:4098949 | G | A | 72 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0063 others(69): Show |
76 | HG00099.hp1 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.919+252C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098949 | |||||||
| chr19:4099092 | G | A | 1 | a0001c0002t0001g0165 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.919+109C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4099092 | |||||||
| chr19:4099189 | T | C | 242 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(239): Show |
257 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.919+12A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4099189 | |||||||
| chr19:4099486 | G | A | 2 | a0001c0001t0001g0274 a0001c0001t0001g0281 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.706-72C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4099486 | |||||||
| chr19:4099893 | G | T | 1 | a0001c0002t0001g0253 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.706-479C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4099893 | |||||||
| chr19:4099961 | C | T | 1 | a0001c0002t0001g0227 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.706-547G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4099961 | |||||||
| chr19:4099976 | A | G | 1 | a0001c0002t0001g0261 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.706-562T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4099976 | |||||||
| chr19:4099978 | G | A | 17 | a0001c0001t0003g0087 a0001c0001t0003g0277 a0001c0001t0004g0300 others(14): Show |
17 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.706-564C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4099978 | |||||||
| chr19:4099989 | C | CCTGTAAT others(12): Show |
1 | a0001c0001t0001g0275 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.706-594_706-576dup others(19): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4099989 | |||||||
| chr19:4100024 | C | A | 1 | a0001c0001t0003g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.706-610G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100024 | |||||||
| chr19:4100033 | A | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0174 a0001c0001t0001g0274 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.706-619T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100033 | |||||||
| chr19:4100042 | T | C | 6 | a0001c0001t0001g0036 a0001c0001t0001g0078 a0001c0001t0001g0104 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.706-628A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100042 | |||||||
| chr19:4100057 | T | G | 306 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(303): Show |
322 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.706-643A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100057 | |||||||
| chr19:4100058 | G | A | 308 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(305): Show |
324 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.706-644C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100058 | |||||||
| chr19:4100060 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.706-646G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100060 | |||||||
| chr19:4100061 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.706-647T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100061 | |||||||
| chr19:4100062 | T | C | 306 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(303): Show |
322 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.706-648A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100062 | |||||||
| chr19:4100073 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.706-659A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100073 | |||||||
| chr19:4100168 | T | C | 1 | a0001c0002t0001g0018 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.706-754A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100168 | |||||||
| chr19:4100177 | C | T | 1 | a0001c0002t0001g0165 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.706-763G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100177 | |||||||
| chr19:4100195 | G | T | 1 | a0001c0003t0001g0096 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.706-781C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100195 | |||||||
| chr19:4100386 | T | C | 1 | a0001c0002t0001g0013 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.705+633A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100386 | |||||||
| chr19:4100428 | T | TGAAA | 4 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0274 others(1): Show |
4 | HG02451.hp2 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+590_705+591ins others(4): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100428 | |||||||
| chr19:4100428 | T | TGAAAA | 4 | a0001c0001t0001g0174 a0001c0001t0001g0281 a0001c0004t0001g0264 others(1): Show |
4 | HG01243.hp2 HG02109.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+590_705+591ins others(5): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100428 | |||||||
| chr19:4100429 | C | A | 8 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0174 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.705+590G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | |||||||
| chr19:4100429 | C | CA | 13 | a0001c0001t0001g0062 a0001c0001t0001g0074 a0001c0001t0001g0078 others(10): Show |
13 | HG00738.hp2 HG01123.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.705+589dupT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | |||||||
| chr19:4100429 | C | CAA | 50 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0063 others(47): Show |
51 | HG00323.hp2 HG01099.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.705+588_705+589dup others(2): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | |||||||
| chr19:4100429 | C | CAAA | 44 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0143 others(41): Show |
48 | HG00423.hp2 HG00597.hp2 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.705+587_705+589dup others(3): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | |||||||
| chr19:4100429 | C | CAAAA | 10 | a0001c0001t0001g0061 a0001c0001t0001g0085 a0001c0001t0001g0154 others(7): Show |
10 | HG00438.hp2 HG01109.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.705+586_705+589dup others(4): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | |||||||
| chr19:4100429 | C | CAAAAA | 9 | a0001c0001t0001g0092 a0001c0001t0001g0105 a0001c0001t0001g0188 others(6): Show |
9 | HG02055.hp2 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.705+585_705+589dup others(5): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | |||||||
| chr19:4100429 | CA | C | 102 | a0001c0001t0001g0043 a0001c0001t0001g0094 a0001c0001t0001g0247 others(99): Show |
110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.705+589delT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | |||||||
| chr19:4100429 | CAA | C | 6 | a0001c0002t0001g0128 a0001c0002t0001g0212 a0001c0002t0001g0221 others(3): Show |
6 | HG00099.hp1 HG01074.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.705+588_705+589del others(2): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | |||||||
| chr19:4100479 | T | C | 2 | a0001c0001t0002g0046 a0001c0001t0002g0137 |
2 | HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.705+540A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100479 | |||||||
| chr19:4100662 | G | A | 255 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0021 others(252): Show |
270 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.705+357C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100662 | |||||||
| chr19:4100665 | A | C | 2 | a0001c0001t0002g0109 a0001c0001t0002g0110 |
2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.705+354T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100665 | |||||||
| chr19:4100682 | T | C | 1 | a0001c0001t0002g0144 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.705+337A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100682 | |||||||
| chr19:4100828 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.705+191A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100828 | |||||||
| chr19:4100840 | A | G | 17 | a0001c0001t0003g0277 a0001c0001t0004g0300 a0001c0001t0004g0301 others(14): Show |
17 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.705+179T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100840 | |||||||
| chr19:4100891 | G | A | 1 | a0001c0005t0003g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.705+128C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100891 | |||||||
| chr19:4101008 | C | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0281 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.705+11G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4101008 | |||||||
| chr19:4101198 | G | A | 2 | a0001c0001t0002g0109 a0001c0001t0002g0110 |
2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.580+31C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 5/10 | chr19 | 4101198 | |||||||
| chr19:4101215 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.580+14C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 5/10 | chr19 | 4101215 | |||||||
| chr19:4101306 | C | T | 7 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0018 others(4): Show |
7 | HG02071.hp1 HG02165.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.529-26G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101306 | |||||||
| chr19:4101387 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.529-107G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101387 | |||||||
| chr19:4101418 | C | T | 7 | a0001c0001t0001g0188 a0001c0004t0001g0067 a0001c0004t0001g0193 others(4): Show |
7 | HG02572.hp2 HG02615.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.529-138G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101418 | |||||||
| chr19:4101436 | G | A | 1 | a0001c0002t0001g0210 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.529-156C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101436 | |||||||
| chr19:4101461 | C | T | 1 | a0001c0002t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.529-181G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101461 | |||||||
| chr19:4101468 | G | A | 1 | a0001c0006t0001g0023 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.529-188C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101468 | |||||||
| chr19:4101478 | G | A | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.529-198C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101478 | |||||||
| chr19:4101516 | C | T | 3 | a0001c0001t0003g0172 a0001c0002t0001g0164 a0001c0002t0001g0165 |
3 | HG02109.hp2 HG02523.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.529-236G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101516 | |||||||
| chr19:4101568 | T | C | 1 | a0001c0002t0001g0216 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.529-288A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101568 | |||||||
| chr19:4101792 | A | C | 3 | a0001c0001t0005g0293 a0001c0006t0001g0273 a0001c0006t0008g0299 |
3 | HG03098.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.529-512T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101792 | |||||||
| chr19:4101845 | C | A | 1 | a0001c0001t0001g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.528+531G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101845 | |||||||
| chr19:4101868 | T | C | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.528+508A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101868 | |||||||
| chr19:4102018 | G | A | 1 | a0001c0002t0001g0255 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.528+358C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102018 | |||||||
| chr19:4102075 | G | A | 1 | a0001c0002t0001g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.528+301C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102075 | |||||||
| chr19:4102134 | A | C | 90 | a0001c0001t0001g0021 a0001c0001t0001g0065 a0001c0001t0001g0074 others(87): Show |
93 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.528+242T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102134 | |||||||
| chr19:4102139 | A | G | 18 | a0001c0001t0001g0036 a0001c0001t0001g0078 a0001c0001t0001g0104 others(15): Show |
19 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.528+237T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102139 | |||||||
| chr19:4102181 | T | C | 3 | a0001c0002t0001g0128 a0001c0003t0001g0082 a0001c0003t0001g0083 |
3 | HG02735.hp1 HG03654.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.528+195A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102181 | |||||||
| chr19:4102199 | A | G | 1 | a0001c0003t0001g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.528+177T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102199 | |||||||
| chr19:4102235 | G | A | 1 | a0001c0001t0005g0293 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.528+141C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102235 | |||||||
| chr19:4102258 | T | C | 9 | a0001c0001t0001g0020 a0001c0001t0003g0035 a0001c0001t0003g0172 others(6): Show |
9 | HG02055.hp2 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.528+118A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102258 | |||||||
| chr19:4102350 | G | A | 2 | a0001c0001t0003g0277 a0001c0001t0004g0304 |
2 | HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.528+26C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102350 | |||||||
| chr19:4102356 | T | C | 15 | a0001c0001t0001g0073 a0001c0001t0001g0104 a0001c0001t0003g0087 others(12): Show |
15 | HG02451.hp1 HG02572.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+20A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102356 | |||||||
| chr19:4102522 | C | A | 1 | a0001c0003t0002g0145 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.451-69G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102522 | |||||||
| chr19:4102522 | C | G | 2 | a0001c0006t0004g0297 a0001c0006t0007g0295 |
2 | HG01109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.451-69G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102522 | |||||||
| chr19:4102554 | C | T | 2 | a0001c0001t0002g0046 a0001c0001t0002g0137 |
2 | HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.451-101G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102554 | |||||||
| chr19:4102588 | G | A | 1 | a0001c0002t0001g0254 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.451-135C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102588 | |||||||
| chr19:4102625 | T | C | 37 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0030 others(34): Show |
38 | HG00621.hp2 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.451-172A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102625 | |||||||
| chr19:4102686 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.451-233G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102686 | |||||||
| chr19:4102716 | G | A | 1 | a0001c0001t0004g0309 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.451-263C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102716 | |||||||
| chr19:4102817 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.451-364C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102817 | |||||||
| chr19:4102822 | G | A | 5 | a0001c0001t0001g0084 a0001c0001t0001g0100 a0001c0001t0001g0106 others(2): Show |
5 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-369C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102822 | |||||||
| chr19:4102836 | G | A | 45 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0029 others(42): Show |
45 | HG00099.hp2 HG00609.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.451-383C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102836 | |||||||
| chr19:4102878 | G | A | 8 | a0001c0001t0001g0050 a0001c0001t0001g0084 a0001c0001t0001g0093 others(5): Show |
8 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-425C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102878 | |||||||
| chr19:4102880 | G | A | 2 | a0001c0002t0001g0176 a0001c0002t0001g0203 |
2 | HG00733.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.451-427C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102880 | |||||||
| chr19:4102898 | G | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0105 others(7): Show |
10 | HG00735.hp2 HG02886.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.451-445C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102898 | |||||||
| chr19:4102922 | C | T | 146 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0065 others(143): Show |
156 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.451-469G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102922 | |||||||
| chr19:4102934 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.451-481C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102934 | |||||||
| chr19:4102941 | G | A | 1 | a0001c0004t0001g0197 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.451-488C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102941 | |||||||
| chr19:4102948 | G | A | 1 | a0001c0002t0007g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.451-495C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102948 | |||||||
| chr19:4102964 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.451-511C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102964 | |||||||
| chr19:4102968 | G | A | 2 | a0001c0003t0005g0286 a0001c0003t0005g0287 |
2 | HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.451-515C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102968 | |||||||
| chr19:4102979 | G | A | 1 | a0001c0001t0004g0310 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.451-526C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102979 | |||||||
| chr19:4103016 | G | A | 2 | a0001c0001t0002g0116 a0001c0002t0001g0168 |
2 | HG01952.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.451-563C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103016 | |||||||
| chr19:4103175 | T | C | 14 | a0001c0001t0001g0278 a0001c0001t0003g0118 a0001c0002t0001g0276 others(11): Show |
15 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.451-722A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103175 | |||||||
| chr19:4103473 | C | T | 1 | a0001c0003t0005g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.451-1020G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103473 | |||||||
| chr19:4103513 | T | TGAGGCTA others(17): Show |
101 | a0001c0001t0001g0065 a0001c0001t0001g0126 a0001c0001t0001g0219 others(98): Show |
107 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.451-1084_451-1061d others(26): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103513 | |||||||
| chr19:4103529 | G | A | 12 | a0001c0002t0007g0284 a0001c0002t0007g0285 a0001c0004t0001g0010 others(9): Show |
13 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-1076C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103529 | |||||||
| chr19:4103664 | C | G | 2 | a0001c0001t0002g0047 a0001c0001t0002g0111 |
2 | HG01192.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.451-1211G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103664 | |||||||
| chr19:4103880 | A | T | 1 | a0001c0002t0001g0244 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.451-1427T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103880 | |||||||
| chr19:4103910 | G | A | 69 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0061 others(66): Show |
74 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.451-1457C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103910 | |||||||
| chr19:4103987 | G | A | 2 | a0001c0001t0002g0112 a0001c0001t0002g0116 |
2 | NA18997.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.451-1534C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103987 | |||||||
| chr19:4104146 | T | C | 1 | a0001c0002t0001g0236 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.451-1693A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104146 | |||||||
| chr19:4104219 | C | T | 1 | a0001c0006t0001g0023 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.451-1766G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104219 | |||||||
| chr19:4104261 | C | T | 1 | a0001c0001t0003g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.451-1808G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104261 | |||||||
| chr19:4104265 | T | TA | 100 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0061 others(97): Show |
109 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.451-1813dupT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104265 | |||||||
| chr19:4104265 | T | TAA | 8 | a0001c0001t0001g0189 a0001c0001t0002g0047 a0001c0001t0002g0120 others(5): Show |
8 | HG01109.hp1 HG01884.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.451-1814_451-1813d others(4): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104265 | |||||||
| chr19:4104265 | TA | T | 11 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0092 others(8): Show |
11 | HG00099.hp1 HG00323.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.451-1813delT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104265 | |||||||
| chr19:4104587 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.451-2134C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104587 | |||||||
| chr19:4104619 | G | T | 1 | a0001c0001t0001g0240 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.451-2166C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104619 | |||||||
| chr19:4104620 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.451-2167G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104620 | |||||||
| chr19:4104673 | G | A | 1 | a0001c0006t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.451-2220C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104673 | |||||||
| chr19:4104717 | C | A | 1 | a0001c0001t0004g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.451-2264G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104717 | |||||||
| chr19:4104817 | C | T | 2 | a0001c0006t0001g0279 a0001c0006t0008g0314 |
2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.451-2364G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104817 | |||||||
| chr19:4104835 | C | T | 2 | a0001c0006t0001g0279 a0001c0006t0008g0314 |
2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.451-2382G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104835 | |||||||
| chr19:4104921 | G | A | 37 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0003g0035 others(34): Show |
41 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.451-2468C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104921 | |||||||
| chr19:4104921 | G | C | 4 | a0001c0001t0001g0056 a0001c0001t0003g0057 a0001c0001t0003g0090 others(1): Show |
4 | HG01099.hp2 HG01192.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-2468C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104921 | |||||||
| chr19:4104940 | T | C | 39 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0003g0035 others(36): Show |
43 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.451-2487A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104940 | |||||||
| chr19:4105155 | C | CGT | 12 | a0001c0001t0001g0029 a0001c0001t0001g0073 a0001c0001t0001g0086 others(9): Show |
12 | HG00323.hp1 HG02155.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.451-2704_451-2703d others(4): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | C | CGTGT | 7 | a0001c0001t0001g0085 a0001c0001t0003g0035 a0001c0001t0003g0118 others(4): Show |
7 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.451-2706_451-2703d others(6): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | C | CGTGTGT | 6 | a0001c0001t0001g0092 a0001c0001t0001g0188 a0001c0001t0004g0301 others(3): Show |
6 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-2708_451-2703d others(8): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | C | CGTGTGTG others(1): Show |
4 | a0001c0001t0004g0304 a0001c0001t0004g0309 a0001c0001t0004g0312 others(1): Show |
4 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-2710_451-2703d others(10): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | C | CGTGTGTG others(3): Show |
2 | a0001c0001t0001g0033 a0001c0002t0007g0294 |
2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.451-2712_451-2703d others(12): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | C | CGTGTGTG others(5): Show |
1 | a0001c0006t0007g0295 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.451-2714_451-2703d others(14): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | C | CGTGTGTG others(7): Show |
1 | a0001c0006t0004g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.451-2716_451-2703d others(16): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | C | CGTGTGTG others(9): Show |
3 | a0001c0001t0003g0087 a0001c0001t0004g0300 a0001c0002t0003g0183 |
3 | HG03139.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.451-2718_451-2703d others(18): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | CGT | C | 45 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0043 others(42): Show |
45 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.451-2704_451-2703d others(4): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | CGTGT | C | 11 | a0001c0001t0001g0032 a0001c0001t0001g0078 a0001c0001t0001g0089 others(8): Show |
15 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.451-2706_451-2703d others(6): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | CGTGTGT | C | 12 | a0001c0001t0002g0045 a0001c0001t0005g0291 a0001c0001t0005g0292 others(9): Show |
12 | HG00408.hp2 HG01081.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.451-2708_451-2703d others(8): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | CGTGTGTG others(1): Show |
C | 34 | a0001c0001t0001g0074 a0001c0001t0001g0084 a0001c0001t0001g0103 others(31): Show |
36 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.451-2710_451-2703d others(10): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | CGTGTGTG others(3): Show |
C | 85 | a0001c0001t0001g0065 a0001c0001t0001g0129 a0001c0001t0001g0219 others(82): Show |
90 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.451-2712_451-2703d others(12): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | CGTGTGTG others(5): Show |
C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0061 others(56): Show |
64 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.451-2714_451-2703d others(14): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0001g0173 a0001c0001t0003g0172 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.451-2716_451-2703d others(16): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0001g0147 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.451-2718_451-2703d others(18): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | CGTGTGTG others(11): Show |
C | 3 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0002g0280 |
3 | NA18979.hp2 NA18993.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.451-2720_451-2703d others(20): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105155 | CGTGTGTG others(15): Show |
C | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.451-2724_451-2703d others(24): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | |||||||
| chr19:4105291 | C | T | 26 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0003g0035 others(23): Show |
29 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.451-2838G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105291 | |||||||
| chr19:4105310 | C | T | 1 | a0001c0002t0001g0211 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.451-2857G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105310 | |||||||
| chr19:4105338 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.451-2885C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105338 | |||||||
| chr19:4105458 | T | C | 244 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(241): Show |
260 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.451-3005A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105458 | |||||||
| chr19:4105458 | T | G | 1 | a0001c0001t0004g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.451-3005A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105458 | |||||||
| chr19:4105494 | G | A | 1 | a0001c0002t0001g0053 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.451-3041C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105494 | |||||||
| chr19:4105561 | C | T | 107 | a0001c0001t0001g0065 a0001c0001t0001g0126 a0001c0001t0001g0219 others(104): Show |
114 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.451-3108G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105561 | |||||||
| chr19:4105564 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.451-3111T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105564 | |||||||
| chr19:4105637 | A | G | 4 | a0001c0006t0001g0022 a0001c0006t0001g0023 a0001c0006t0001g0024 others(1): Show |
4 | HG00408.hp2 NA18747.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-3184T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105637 | |||||||
| chr19:4105708 | G | A | 1 | a0001c0001t0004g0301 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.451-3255C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105708 | |||||||
| chr19:4105853 | G | A | 17 | a0001c0001t0001g0032 a0001c0001t0001g0274 a0001c0001t0001g0278 others(14): Show |
17 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.451-3400C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105853 | |||||||
| chr19:4106131 | G | A | 3 | a0001c0001t0004g0300 a0001c0006t0004g0297 a0001c0006t0007g0295 |
3 | HG01109.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.451-3678C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4106131 | |||||||
| chr19:4106233 | C | A | 111 | a0001c0001t0001g0065 a0001c0001t0001g0126 a0001c0001t0001g0219 others(108): Show |
118 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.451-3780G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4106233 | |||||||
| chr19:4106494 | C | T | 6 | a0001c0001t0005g0288 a0001c0001t0005g0289 a0001c0001t0005g0291 others(3): Show |
6 | HG02886.hp1 HG02922.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+4015G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4106494 | |||||||
| chr19:4106495 | G | A | 1 | a0001c0002t0001g0135 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.450+4014C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4106495 | |||||||
| chr19:4106537 | G | T | 244 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(241): Show |
260 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.450+3972C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4106537 | |||||||
| chr19:4106731 | AC | A | 17 | a0001c0001t0003g0277 a0001c0001t0004g0300 a0001c0001t0004g0301 others(14): Show |
17 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.450+3777delG | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4106731 | |||||||
| chr19:4107111 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.450+3398G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107111 | |||||||
| chr19:4107343 | C | A | 2 | a0001c0006t0001g0279 a0001c0006t0008g0314 |
2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.450+3166G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107343 | |||||||
| chr19:4107352 | G | A | 1 | a0001c0001t0002g0125 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.450+3157C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107352 | |||||||
| chr19:4107397 | G | A | 1 | a0001c0002t0001g0243 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.450+3112C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107397 | |||||||
| chr19:4107518 | C | T | 1 | a0001c0002t0001g0210 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.450+2991G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107518 | |||||||
| chr19:4107523 | C | CA | 36 | a0001c0001t0001g0030 a0001c0001t0001g0126 a0001c0001t0001g0247 others(33): Show |
37 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.450+2985dupT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107523 | |||||||
| chr19:4107523 | CA | C | 67 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0033 others(64): Show |
67 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.450+2985delT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107523 | |||||||
| chr19:4107523 | CAA | C | 63 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0061 others(60): Show |
68 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.450+2984_450+2985d others(4): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107523 | |||||||
| chr19:4107541 | A | C | 1 | a0001c0001t0001g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.450+2968T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107541 | |||||||
| chr19:4107559 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.450+2950C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107559 | |||||||
| chr19:4107665 | C | A | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+2844G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107665 | |||||||
| chr19:4107670 | G | A | 65 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(62): Show |
65 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.450+2839C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107670 | |||||||
| chr19:4107718 | A | C | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+2791T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107718 | |||||||
| chr19:4107807 | C | T | 2 | a0001c0006t0001g0279 a0001c0006t0008g0314 |
2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.450+2702G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107807 | |||||||
| chr19:4107814 | T | C | 3 | a0001c0002t0007g0284 a0001c0002t0007g0285 a0003c0010t0003g0270 |
3 | HG02486.hp1 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+2695A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107814 | |||||||
| chr19:4107872 | C | G | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+2637G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107872 | |||||||
| chr19:4107932 | G | A | 7 | a0001c0006t0001g0273 a0001c0006t0001g0279 a0001c0006t0004g0297 others(4): Show |
7 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+2577C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107932 | |||||||
| chr19:4107938 | G | A | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+2571C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107938 | |||||||
| chr19:4107961 | C | T | 2 | a0001c0001t0001g0274 a0001c0002t0001g0037 |
2 | HG02970.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.450+2548G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107961 | |||||||
| chr19:4107968 | T | G | 4 | a0001c0001t0001g0056 a0001c0001t0003g0057 a0001c0001t0003g0090 others(1): Show |
4 | HG01099.hp2 HG01192.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+2541A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107968 | |||||||
| chr19:4107973 | C | T | 112 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0001g0126 others(109): Show |
119 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.450+2536G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107973 | |||||||
| chr19:4107982 | A | G | 1 | a0001c0002t0002g0280 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.450+2527T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107982 | |||||||
| chr19:4108008 | C | T | 1 | a0003c0010t0003g0270 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.450+2501G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108008 | |||||||
| chr19:4108271 | C | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0063 others(19): Show |
23 | HG01168.hp2 HG01358.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.450+2238G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108271 | |||||||
| chr19:4108279 | G | C | 286 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(283): Show |
301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.450+2230C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108279 | |||||||
| chr19:4108280 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.450+2229C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108280 | |||||||
| chr19:4108286 | G | A | 1 | a0001c0006t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.450+2223C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108286 | |||||||
| chr19:4108346 | T | C | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+2163A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108346 | |||||||
| chr19:4108418 | A | AT | 8 | a0001c0001t0001g0281 a0001c0002t0001g0040 a0001c0002t0001g0054 others(5): Show |
8 | HG01175.hp1 HG01243.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+2090dupA | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108418 | |||||||
| chr19:4108418 | AT | A | 67 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0061 others(64): Show |
72 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.450+2090delA | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108418 | |||||||
| chr19:4108650 | C | T | 1 | a0001c0002t0003g0183 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.450+1859G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108650 | |||||||
| chr19:4108760 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.450+1749C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108760 | |||||||
| chr19:4108847 | C | G | 2 | a0001c0006t0001g0279 a0001c0006t0008g0314 |
2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.450+1662G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108847 | |||||||
| chr19:4108923 | G | A | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+1586C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108923 | |||||||
| chr19:4109033 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0281 |
2 | HG01243.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.450+1476T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109033 | |||||||
| chr19:4109095 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.450+1414C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109095 | |||||||
| chr19:4109107 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.450+1402C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109107 | |||||||
| chr19:4109297 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.450+1212C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109297 | |||||||
| chr19:4109414 | T | C | 2 | a0001c0001t0004g0312 a0001c0001t0004g0313 |
2 | HG02257.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.450+1095A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109414 | |||||||
| chr19:4109500 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.450+1009C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109500 | |||||||
| chr19:4109682 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.450+827G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109682 | |||||||
| chr19:4109782 | G | T | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+727C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109782 | |||||||
| chr19:4109795 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0003g0172 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.450+714T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109795 | |||||||
| chr19:4109796 | T | C | 15 | a0001c0005t0001g0271 a0001c0005t0003g0002 a0001c0005t0003g0042 others(12): Show |
18 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.450+713A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109796 | |||||||
| chr19:4109928 | T | C | 22 | a0001c0001t0001g0188 a0001c0001t0003g0035 a0001c0001t0003g0122 others(19): Show |
23 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.450+581A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109928 | |||||||
| chr19:4110032 | G | A | 285 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(282): Show |
300 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.450+477C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4110032 | |||||||
| chr19:4110148 | A | T | 1 | a0001c0002t0009g0282 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.450+361T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4110148 | |||||||
| chr19:4110320 | G | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0061 others(67): Show |
75 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.450+189C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4110320 | |||||||
| chr19:4110410 | T | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0061 others(68): Show |
76 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.450+99A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4110410 | |||||||
| chr19:4110469 | G | A | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+40C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4110469 | |||||||
| chr19:4110494 | C | A | 12 | a0001c0002t0001g0276 a0001c0004t0001g0010 a0001c0004t0001g0067 others(9): Show |
13 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.450+15G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4110494 | |||||||
| chr19:4110782 | C | T | 3 | a0001c0001t0004g0301 a0001c0001t0004g0304 a0001c0001t0004g0305 |
3 | HG02896.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.304-127G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4110782 | |||||||
| chr19:4110982 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.304-327C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4110982 | |||||||
| chr19:4111023 | C | A | 11 | a0001c0004t0001g0010 a0001c0004t0001g0067 a0001c0004t0001g0191 others(8): Show |
12 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.304-368G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111023 | |||||||
| chr19:4111024 | G | A | 1 | a0001c0002t0001g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.304-369C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111024 | |||||||
| chr19:4111092 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.304-437A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111092 | |||||||
| chr19:4111159 | T | C | 1 | a0001c0002t0001g0064 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.304-504A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111159 | |||||||
| chr19:4111234 | T | C | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.304-579A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111234 | |||||||
| chr19:4111511 | C | A | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.304-856G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111511 | |||||||
| chr19:4111761 | C | T | 109 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0001g0219 others(106): Show |
116 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.304-1106G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111761 | |||||||
| chr19:4111765 | C | T | 2 | a0001c0001t0004g0302 a0001c0001t0004g0303 |
2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.304-1110G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111765 | |||||||
| chr19:4111783 | G | A | 20 | a0001c0001t0001g0084 a0001c0001t0001g0100 a0001c0001t0001g0106 others(17): Show |
20 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.304-1128C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111783 | |||||||
| chr19:4111810 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.304-1155C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111810 | |||||||
| chr19:4111845 | C | G | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1190G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111845 | |||||||
| chr19:4111846 | G | C | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1191C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111846 | |||||||
| chr19:4111907 | C | T | 1 | a0001c0001t0003g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.304-1252G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111907 | |||||||
| chr19:4111927 | T | C | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1272A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111927 | |||||||
| chr19:4111928 | G | T | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1273C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111928 | |||||||
| chr19:4111960 | A | C | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1305T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111960 | |||||||
| chr19:4111965 | C | A | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1310G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111965 | |||||||
| chr19:4111966 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.304-1311T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111966 | |||||||
| chr19:4111975 | AAAC | A | 15 | a0001c0001t0003g0277 a0001c0001t0004g0300 a0001c0001t0004g0301 others(12): Show |
15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.304-1323_304-1321d others(5): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111975 | |||||||
| chr19:4111975 | AAACAAC | A | 23 | a0001c0001t0001g0281 a0001c0005t0001g0271 a0001c0005t0003g0002 others(20): Show |
26 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.304-1326_304-1321d others(8): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111975 | |||||||
| chr19:4111987 | C | CAA | 10 | a0001c0004t0001g0010 a0001c0004t0001g0067 a0001c0004t0001g0191 others(7): Show |
11 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.304-1334_304-1333d others(4): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111987 | |||||||
| chr19:4111990 | C | A | 10 | a0001c0004t0001g0010 a0001c0004t0001g0067 a0001c0004t0001g0191 others(7): Show |
11 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.304-1335G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111990 | |||||||
| chr19:4111993 | C | A | 13 | a0001c0002t0007g0284 a0001c0002t0007g0285 a0001c0004t0001g0010 others(10): Show |
14 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.304-1338G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111993 | |||||||
| chr19:4111996 | C | A | 14 | a0001c0001t0001g0174 a0001c0002t0007g0284 a0001c0002t0007g0285 others(11): Show |
15 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.304-1341G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111996 | |||||||
| chr19:4112082 | T | G | 109 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0001g0219 others(106): Show |
116 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.304-1427A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112082 | |||||||
| chr19:4112138 | A | G | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1483T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112138 | |||||||
| chr19:4112139 | G | A | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1484C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112139 | |||||||
| chr19:4112148 | A | T | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1493T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112148 | |||||||
| chr19:4112149 | T | G | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1494A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112149 | |||||||
| chr19:4112151 | G | T | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1496C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112151 | |||||||
| chr19:4112230 | C | A | 1 | a0001c0001t0001g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.304-1575G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112230 | |||||||
| chr19:4112247 | G | A | 11 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0003g0035 others(8): Show |
11 | HG01884.hp1 HG02055.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.304-1592C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112247 | |||||||
| chr19:4112327 | T | C | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1672A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112327 | |||||||
| chr19:4112328 | G | T | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1673C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112328 | |||||||
| chr19:4112354 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.304-1699A>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112354 | |||||||
| chr19:4112434 | C | T | 1 | a0001c0005t0003g0269 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.304-1779G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112434 | |||||||
| chr19:4112480 | A | G | 247 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(244): Show |
263 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.304-1825T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112480 | |||||||
| chr19:4112578 | G | A | 4 | a0001c0002t0001g0054 a0001c0002t0001g0178 a0001c0002t0001g0244 others(1): Show |
4 | HG02273.hp2 NA18955.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-1923C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112578 | |||||||
| chr19:4112582 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.304-1927G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112582 | |||||||
| chr19:4112639 | C | T | 1 | a0001c0002t0001g0179 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.304-1984G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112639 | |||||||
| chr19:4112644 | C | CCCTGGCG others(3): Show |
15 | a0001c0001t0003g0277 a0001c0001t0004g0300 a0001c0001t0004g0301 others(12): Show |
15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.304-1999_304-1990d others(12): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112644 | |||||||
| chr19:4112665 | C | T | 1 | a0001c0002t0001g0160 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.304-2010G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112665 | |||||||
| chr19:4112737 | C | T | 1 | a0001c0003t0001g0102 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.304-2082G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112737 | |||||||
| chr19:4112749 | G | A | 73 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0036 others(70): Show |
78 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.304-2094C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112749 | |||||||
| chr19:4112801 | C | A | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-2146G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112801 | |||||||
| chr19:4112897 | C | T | 109 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0001g0219 others(106): Show |
116 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.304-2242G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112897 | |||||||
| chr19:4112989 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.304-2334G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112989 | |||||||
| chr19:4112990 | G | A | 106 | a0001c0001t0001g0065 a0001c0001t0001g0219 a0001c0001t0001g0231 others(103): Show |
113 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.304-2335C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112990 | |||||||
| chr19:4113105 | G | C | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-2450C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113105 | |||||||
| chr19:4113115 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.304-2460G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113115 | |||||||
| chr19:4113116 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.304-2461C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113116 | |||||||
| chr19:4113145 | T | C | 1 | a0001c0002t0001g0040 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.304-2490A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113145 | |||||||
| chr19:4113314 | T | G | 12 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0003g0035 others(9): Show |
12 | HG01884.hp1 HG02055.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.304-2659A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113314 | |||||||
| chr19:4113316 | A | G | 5 | a0001c0006t0001g0273 a0001c0006t0004g0297 a0001c0006t0007g0295 others(2): Show |
5 | HG01109.hp2 HG03098.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-2661T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113316 | |||||||
| chr19:4113340 | G | C | 15 | a0001c0001t0003g0277 a0001c0001t0004g0300 a0001c0001t0004g0301 others(12): Show |
15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.304-2685C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113340 | |||||||
| chr19:4113500 | C | T | 15 | a0001c0001t0003g0277 a0001c0001t0004g0300 a0001c0001t0004g0301 others(12): Show |
15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.304-2845G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113500 | |||||||
| chr19:4113854 | C | G | 1 | a0001c0001t0003g0277 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.304-3199G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113854 | |||||||
| chr19:4113865 | C | A | 1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-3210G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113865 | |||||||
| chr19:4113868 | C | T | 11 | a0001c0004t0001g0010 a0001c0004t0001g0067 a0001c0004t0001g0191 others(8): Show |
12 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.304-3213G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113868 | |||||||
| chr19:4113952 | G | C | 1 | a0001c0001t0001g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.304-3297C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113952 | |||||||
| chr19:4113983 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.304-3328C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113983 | |||||||
| chr19:4114162 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0092 others(1): Show |
4 | HG02572.hp1 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+3257A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114162 | |||||||
| chr19:4114204 | G | A | 22 | a0001c0005t0001g0271 a0001c0005t0003g0002 a0001c0005t0003g0042 others(19): Show |
25 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.303+3215C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114204 | |||||||
| chr19:4114312 | T | C | 249 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(246): Show |
265 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.303+3107A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114312 | |||||||
| chr19:4114362 | C | G | 1 | a0001c0001t0003g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.303+3057G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114362 | |||||||
| chr19:4114417 | G | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0061 others(69): Show |
77 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.303+3002C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114417 | |||||||
| chr19:4114549 | C | T | 2 | a0001c0001t0001g0247 a0001c0002t0001g0205 |
2 | HG00423.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.303+2870G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114549 | |||||||
| chr19:4114568 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.303+2851C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114568 | |||||||
| chr19:4114581 | C | T | 1 | a0001c0002t0001g0253 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.303+2838G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114581 | |||||||
| chr19:4114610 | C | G | 5 | a0001c0006t0001g0273 a0001c0006t0004g0297 a0001c0006t0007g0295 others(2): Show |
5 | HG01109.hp2 HG03098.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.303+2809G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114610 | |||||||
| chr19:4114620 | G | A | 1 | a0001c0002t0001g0179 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.303+2799C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114620 | |||||||
| chr19:4114724 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.303+2695C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114724 | |||||||
| chr19:4114778 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.303+2641C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114778 | |||||||
| chr19:4114840 | G | A | 1 | a0001c0002t0001g0053 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.303+2579C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114840 | |||||||
| chr19:4114917 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.303+2502C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114917 | |||||||
| chr19:4115127 | G | A | 1 | a0001c0003t0001g0102 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.303+2292C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115127 | |||||||
| chr19:4115324 | C | T | 9 | a0001c0001t0001g0188 a0001c0001t0003g0035 a0001c0001t0003g0190 others(6): Show |
9 | HG01884.hp1 HG02055.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.303+2095G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115324 | |||||||
| chr19:4115395 | C | T | 2 | a0001c0003t0005g0286 a0001c0003t0005g0287 |
2 | HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.303+2024G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115395 | |||||||
| chr19:4115454 | G | A | 17 | a0001c0005t0001g0271 a0001c0005t0003g0002 a0001c0005t0003g0042 others(14): Show |
20 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.303+1965C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115454 | |||||||
| chr19:4115564 | G | A | 142 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0001g0219 others(139): Show |
150 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.303+1855C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115564 | |||||||
| chr19:4115686 | G | A | 15 | a0001c0005t0001g0271 a0001c0005t0003g0002 a0001c0005t0003g0042 others(12): Show |
18 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.303+1733C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115686 | |||||||
| chr19:4115719 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.303+1700C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115719 | |||||||
| chr19:4115773 | C | T | 2 | a0001c0006t0001g0279 a0001c0006t0008g0314 |
2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.303+1646G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115773 | |||||||
| chr19:4115848 | G | A | 1 | a0001c0007t0001g0248 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.303+1571C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115848 | |||||||
| chr19:4115853 | G | A | 2 | a0001c0006t0001g0279 a0001c0006t0008g0314 |
2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.303+1566C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115853 | |||||||
| chr19:4115857 | C | G | 1 | a0001c0002t0001g0204 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.303+1562G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115857 | |||||||
| chr19:4115995 | G | A | 76 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0036 others(73): Show |
81 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.303+1424C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115995 | |||||||
| chr19:4116083 | A | T | 11 | a0001c0005t0003g0002 a0001c0005t0003g0042 a0001c0005t0003g0072 others(8): Show |
14 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.303+1336T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116083 | |||||||
| chr19:4116107 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.303+1312G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116107 | |||||||
| chr19:4116142 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.303+1277T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116142 | |||||||
| chr19:4116164 | T | C | 251 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(248): Show |
267 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.303+1255A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116164 | |||||||
| chr19:4116199 | AG | A | 15 | a0001c0005t0001g0271 a0001c0005t0003g0002 a0001c0005t0003g0042 others(12): Show |
18 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.303+1219delC | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116199 | |||||||
| chr19:4116200 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.303+1219C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116200 | |||||||
| chr19:4116337 | C | G | 88 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0036 others(85): Show |
93 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.303+1082G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116337 | |||||||
| chr19:4116349 | G | A | 1 | a0001c0002t0001g0276 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.303+1070C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116349 | |||||||
| chr19:4116419 | A | G | 2 | a0001c0002t0001g0176 a0001c0002t0001g0203 |
2 | HG00733.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.303+1000T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116419 | |||||||
| chr19:4116476 | G | T | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.303+943C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116476 | |||||||
| chr19:4116586 | C | T | 1 | a0001c0001t0003g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.303+833G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116586 | |||||||
| chr19:4116592 | C | T | 2 | a0001c0003t0001g0012 a0001c0007t0001g0019 |
2 | NA18983.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.303+827G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116592 | |||||||
| chr19:4116632 | G | C | 2 | a0001c0002t0001g0249 a0001c0002t0001g0254 |
2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.303+787C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116632 | |||||||
| chr19:4116649 | A | C | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.303+770T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116649 | |||||||
| chr19:4116654 | A | G | 251 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(248): Show |
267 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.303+765T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116654 | |||||||
| chr19:4116703 | G | A | 1 | a0001c0002t0001g0250 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.303+716C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116703 | |||||||
| chr19:4116715 | G | A | 22 | a0001c0005t0001g0271 a0001c0005t0003g0002 a0001c0005t0003g0042 others(19): Show |
25 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.303+704C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116715 | |||||||
| chr19:4116732 | A | T | 1 | a0001c0001t0001g0085 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.303+687T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116732 | |||||||
| chr19:4116778 | A | G | 4 | a0001c0002t0001g0068 a0001c0002t0001g0077 a0001c0002t0001g0202 others(1): Show |
4 | NA18950.hp1 NA18975.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+641T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116778 | |||||||
| chr19:4116881 | A | G | 1 | a0001c0002t0001g0276 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.303+538T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116881 | |||||||
| chr19:4117040 | C | T | 10 | a0001c0001t0001g0061 a0001c0001t0001g0126 a0001c0001t0002g0006 others(7): Show |
11 | HG00423.hp2 HG00438.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.303+379G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117040 | |||||||
| chr19:4117054 | T | G | 1 | a0001c0001t0001g0281 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.303+365A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117054 | |||||||
| chr19:4117239 | C | T | 1 | a0001c0001t0003g0190 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.303+180G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117239 | |||||||
| chr19:4117290 | GGTGGGGA others(30): Show |
G | 1 | a0001c0002t0003g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.303+92_303+128delA others(36): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117290 | |||||||
| chr19:4117292 | T | C | 251 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(248): Show |
267 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.303+127A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117292 | |||||||
| chr19:4117301 | G | C | 3 | a0001c0001t0001g0074 a0001c0001t0002g0034 a0001c0001t0002g0045 |
3 | HG01433.hp2 HG02055.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.303+118C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117301 | |||||||
| chr19:4117338 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0002g0113 a0001c0001t0002g0153 |
3 | HG00438.hp2 HG02015.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.303+81C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117338 | |||||||
| chr19:4117401 | C | T | 1 | a0001c0003t0001g0201 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.303+18G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117401 | |||||||
| chr19:4117411 | G | C | 1 | a0001c0002t0001g0276 | 1 | HG02723.hp1 | splice_region_variant&intron_variant | LOW | c.303+8C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117411 | |||||||
| chr19:4117412 | T | C | 1 | a0001c0007t0001g0019 | 1 | NA18983.hp1 | splice_region_variant&intron_variant | LOW | c.303+7A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117412 | |||||||
| chr19:4117707 | T | C | 252 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(249): Show |
268 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.93-78A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4117707 | |||||||
| chr19:4117798 | C | T | 1 | a0001c0002t0001g0199 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.93-169G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4117798 | |||||||
| chr19:4117820 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.93-191G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4117820 | |||||||
| chr19:4117841 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.93-212G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4117841 | |||||||
| chr19:4117871 | G | T | 3 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0003g0087 |
3 | HG02572.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.93-242C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4117871 | |||||||
| chr19:4117960 | C | T | 1 | a0001c0001t0003g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.93-331G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4117960 | |||||||
| chr19:4117961 | G | A | 5 | a0001c0001t0001g0114 a0001c0001t0001g0154 a0001c0001t0001g0155 others(2): Show |
5 | NA18948.hp1 NA18962.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.93-332C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4117961 | |||||||
| chr19:4118001 | G | A | 1 | a0001c0002t0001g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.93-372C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118001 | |||||||
| chr19:4118027 | T | G | 1 | a0001c0001t0001g0281 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.93-398A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118027 | |||||||
| chr19:4118166 | G | A | 1 | a0001c0002t0002g0252 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.93-537C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118166 | |||||||
| chr19:4118182 | C | A | 1 | a0001c0001t0001g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-553G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118182 | |||||||
| chr19:4118217 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.93-588G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118217 | |||||||
| chr19:4118268 | G | A | 1 | a0001c0002t0001g0276 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.93-639C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118268 | |||||||
| chr19:4118326 | A | AG | 22 | a0001c0005t0001g0271 a0001c0005t0003g0002 a0001c0005t0003g0042 others(19): Show |
25 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.93-698_93-697insC | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118326 | |||||||
| chr19:4118376 | A | T | 1 | a0001c0001t0001g0043 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.93-747T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118376 | |||||||
| chr19:4118451 | C | T | 1 | a0001c0002t0001g0052 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.93-822G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118451 | |||||||
| chr19:4118483 | A | G | 252 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(249): Show |
268 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.93-854T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118483 | |||||||
| chr19:4118508 | G | C | 7 | a0001c0006t0001g0273 a0001c0006t0001g0279 a0001c0006t0004g0297 others(4): Show |
7 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.93-879C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118508 | |||||||
| chr19:4118508 | G | T | 15 | a0001c0005t0001g0271 a0001c0005t0003g0002 a0001c0005t0003g0042 others(12): Show |
18 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.93-879C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118508 | |||||||
| chr19:4118600 | C | CA | 5 | a0001c0001t0001g0103 a0001c0002t0001g0064 a0001c0002t0001g0253 others(2): Show |
5 | HG00741.hp1 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-972dupT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118600 | |||||||
| chr19:4118718 | A | G | 252 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(249): Show |
268 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.93-1089T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118718 | |||||||
| chr19:4118873 | T | C | 139 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0036 others(136): Show |
148 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.93-1244A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118873 | |||||||
| chr19:4118901 | A | G | 139 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0036 others(136): Show |
148 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.93-1272T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118901 | |||||||
| chr19:4118954 | T | C | 1 | a0001c0002t0001g0262 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.93-1325A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118954 | |||||||
| chr19:4119014 | A | G | 278 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(275): Show |
294 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.93-1385T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119014 | |||||||
| chr19:4119024 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.93-1395T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119024 | |||||||
| chr19:4119288 | C | G | 1 | a0001c0001t0001g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.93-1659G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119288 | |||||||
| chr19:4119326 | A | G | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.93-1697T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119326 | |||||||
| chr19:4119381 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.93-1752G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119381 | |||||||
| chr19:4119492 | G | T | 1 | a0001c0001t0001g0043 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.93-1863C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119492 | |||||||
| chr19:4119527 | T | G | 15 | a0001c0001t0003g0277 a0001c0001t0004g0300 a0001c0001t0004g0301 others(12): Show |
15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.93-1898A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119527 | |||||||
| chr19:4119590 | T | G | 15 | a0001c0001t0003g0277 a0001c0001t0004g0300 a0001c0001t0004g0301 others(12): Show |
15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.93-1961A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119590 | |||||||
| chr19:4119785 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.93-2156A>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119785 | |||||||
| chr19:4119818 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.93-2189T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119818 | |||||||
| chr19:4119921 | G | A | 2 | a0001c0003t0001g0157 a0001c0003t0001g0158 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.93-2292C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119921 | |||||||
| chr19:4119929 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.93-2300G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119929 | |||||||
| chr19:4120145 | C | A | 15 | a0001c0001t0003g0277 a0001c0001t0004g0300 a0001c0001t0004g0301 others(12): Show |
15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.93-2516G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120145 | |||||||
| chr19:4120177 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-2548T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120177 | |||||||
| chr19:4120193 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.93-2564C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120193 | |||||||
| chr19:4120282 | A | G | 1 | a0001c0006t0001g0279 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.93-2653T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120282 | |||||||
| chr19:4120305 | C | A | 1 | a0001c0001t0001g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.93-2676G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120305 | |||||||
| chr19:4120332 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.93-2703A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120332 | |||||||
| chr19:4120469 | G | A | 180 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(177): Show |
188 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.93-2840C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120469 | |||||||
| chr19:4120587 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.93-2958C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120587 | |||||||
| chr19:4120596 | C | T | 7 | a0001c0006t0001g0273 a0001c0006t0001g0279 a0001c0006t0004g0297 others(4): Show |
7 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.93-2967G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120596 | |||||||
| chr19:4120663 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0002g0005 a0001c0001t0002g0060 others(5): Show |
10 | HG01109.hp1 HG01123.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.93-3034G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120663 | |||||||
| chr19:4120745 | A | T | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.92+3039T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120745 | |||||||
| chr19:4120787 | T | C | 2 | a0001c0002t0001g0256 a0001c0002t0001g0257 |
2 | HG02040.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.92+2997A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120787 | |||||||
| chr19:4120829 | G | A | 1 | a0001c0001t0003g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.92+2955C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120829 | |||||||
| chr19:4120848 | C | T | 74 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0061 others(71): Show |
79 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.92+2936G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120848 | |||||||
| chr19:4120853 | TCTGTGCA others(87): Show |
T | 1 | a0001c0001t0001g0084 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.92+2837_92+2930del others(94): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120853 | |||||||
| chr19:4120925 | G | C | 30 | a0001c0001t0001g0050 a0001c0001t0001g0079 a0001c0001t0001g0081 others(27): Show |
30 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.92+2859C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120925 | |||||||
| chr19:4120990 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.92+2794G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120990 | |||||||
| chr19:4121028 | C | T | 15 | a0001c0005t0001g0271 a0001c0005t0003g0002 a0001c0005t0003g0042 others(12): Show |
18 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.92+2756G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121028 | |||||||
| chr19:4121070 | C | A | 1 | a0001c0002t0001g0258 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.92+2714G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121070 | |||||||
| chr19:4121119 | C | T | 1 | a0001c0001t0003g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.92+2665G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121119 | |||||||
| chr19:4121197 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.92+2587G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121197 | |||||||
| chr19:4121382 | T | C | 5 | a0001c0006t0001g0273 a0001c0006t0004g0297 a0001c0006t0007g0295 others(2): Show |
5 | HG01109.hp2 HG03098.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.92+2402A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121382 | |||||||
| chr19:4121414 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.92+2370T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121414 | |||||||
| chr19:4121434 | A | G | 11 | a0001c0004t0001g0010 a0001c0004t0001g0067 a0001c0004t0001g0191 others(8): Show |
12 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.92+2350T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121434 | |||||||
| chr19:4121650 | C | A | 1 | a0001c0001t0001g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+2134G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121650 | |||||||
| chr19:4121653 | C | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0105 |
2 | HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.92+2131G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121653 | |||||||
| chr19:4121726 | ACCCGCTA others(16): Show |
A | 1 | a0001c0001t0001g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.92+2035_92+2057del others(23): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121726 | |||||||
| chr19:4121729 | C | T | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.92+2055G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121729 | |||||||
| chr19:4121762 | C | T | 1 | a0001c0002t0001g0276 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92+2022G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121762 | |||||||
| chr19:4121833 | C | CT | 122 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0061 others(119): Show |
130 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.92+1950_92+1951ins others(1): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121833 | |||||||
| chr19:4121844 | G | A | 1 | a0001c0001t0004g0301 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.92+1940C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121844 | |||||||
| chr19:4121921 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.92+1863C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121921 | |||||||
| chr19:4121937 | C | T | 2 | a0001c0002t0007g0284 a0001c0002t0007g0285 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.92+1847G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121937 | |||||||
| chr19:4121958 | T | C | 1 | a0001c0001t0003g0190 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.92+1826A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121958 | |||||||
| chr19:4121988 | C | A | 1 | a0001c0002t0001g0055 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.92+1796G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121988 | |||||||
| chr19:4122013 | C | T | 5 | a0001c0001t0001g0081 a0001c0001t0002g0080 a0001c0003t0001g0058 others(2): Show |
5 | HG03239.hp1 HG03654.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.92+1771G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122013 | |||||||
| chr19:4122082 | C | A | 1 | a0001c0002t0001g0276 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92+1702G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122082 | |||||||
| chr19:4122086 | T | TC | 10 | a0001c0001t0002g0046 a0001c0001t0002g0048 a0001c0002t0001g0077 others(7): Show |
10 | HG00735.hp1 HG01123.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.92+1697dupG | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122086 | |||||||
| chr19:4122091 | G | C | 1 | a0001c0002t0001g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.92+1693C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122091 | |||||||
| chr19:4122157 | C | CACCCTCC others(204): Show |
1 | a0001c0002t0001g0064 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.92+1626_92+1627ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122157 | |||||||
| chr19:4122187 | A | AACCCTCC others(170): Show |
1 | a0001c0002t0001g0040 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(177): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(293): Show |
1 | a0001c0001t0002g0117 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(300): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(173): Show |
1 | a0001c0001t0001g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(113): Show |
7 | a0001c0006t0001g0273 a0001c0006t0001g0279 a0001c0006t0004g0297 others(4): Show |
7 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(120): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(173): Show |
1 | a0001c0001t0002g0048 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(173): Show |
1 | a0001c0001t0001g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(203): Show |
13 | a0001c0001t0001g0159 a0001c0002t0001g0009 a0001c0002t0001g0160 others(10): Show |
14 | HG01069.hp2 HG01074.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(210): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(174): Show |
4 | a0001c0001t0001g0065 a0001c0002t0001g0053 a0001c0002t0001g0181 others(1): Show |
4 | HG00735.hp1 HG03492.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(181): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(174): Show |
8 | a0001c0002t0001g0052 a0001c0002t0001g0076 a0001c0002t0001g0176 others(5): Show |
8 | HG00733.hp2 HG01175.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(181): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(143): Show |
1 | a0001c0002t0001g0262 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(150): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(173): Show |
1 | a0001c0002t0001g0261 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(143): Show |
7 | a0001c0001t0002g0229 a0001c0002t0001g0199 a0001c0002t0001g0209 others(4): Show |
7 | HG02165.hp2 NA18943.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(150): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(173): Show |
83 | a0001c0001t0001g0032 a0001c0001t0001g0219 a0001c0001t0001g0231 others(80): Show |
90 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(174): Show |
1 | a0001c0002t0001g0180 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(181): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(204): Show |
2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02976.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(203): Show |
5 | a0001c0001t0001g0106 a0001c0001t0005g0291 a0001c0001t0005g0292 others(2): Show |
5 | HG01261.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(210): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(203): Show |
49 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(46): Show |
49 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(210): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(173): Show |
1 | a0001c0001t0001g0281 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(173): Show |
1 | a0001c0002t0001g0276 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(204): Show |
1 | a0001c0002t0007g0285 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(174): Show |
1 | a0001c0001t0003g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(181): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | AACCCTCC others(173): Show |
9 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0003g0190 others(6): Show |
9 | HG01884.hp1 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122187 | A | G | 3 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0002t0001g0064 |
3 | HG03942.hp2 HG04184.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.92+1597T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | |||||||
| chr19:4122194 | C | CCACCCCA others(113): Show |
15 | a0001c0001t0003g0277 a0001c0001t0004g0300 a0001c0001t0004g0301 others(12): Show |
15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.92+1589_92+1590ins others(120): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122194 | |||||||
| chr19:4122224 | C | CCACCCCA others(55): Show |
1 | a0001c0005t0003g0042 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.92+1559_92+1560ins others(62): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122224 | |||||||
| chr19:4122224 | C | CCACCCCA others(54): Show |
1 | a0001c0011t0001g0265 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.92+1559_92+1560ins others(61): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122224 | |||||||
| chr19:4122224 | C | CCACCCCA others(53): Show |
13 | a0001c0005t0001g0271 a0001c0005t0003g0002 a0001c0005t0003g0072 others(10): Show |
16 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.92+1559_92+1560ins others(60): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122224 | |||||||
| chr19:4122233 | C | G | 1 | a0001c0002t0007g0284 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.92+1551G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122233 | |||||||
| chr19:4122247 | G | A | 16 | a0001c0001t0001g0159 a0001c0001t0002g0048 a0001c0001t0002g0117 others(13): Show |
17 | HG01069.hp2 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.92+1537C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | |||||||
| chr19:4122247 | G | GACCCTCC others(202): Show |
1 | a0001c0001t0001g0115 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.92+1536_92+1537ins others(209): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | |||||||
| chr19:4122247 | G | GACCCTCC others(205): Show |
1 | a0001c0001t0002g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.92+1536_92+1537ins others(212): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | |||||||
| chr19:4122247 | G | GACCCTCC others(204): Show |
5 | a0001c0001t0001g0061 a0001c0001t0001g0074 a0001c0001t0001g0114 others(2): Show |
5 | HG00438.hp2 HG01433.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.92+1536_92+1537ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | |||||||
| chr19:4122247 | G | GACCCTCC others(204): Show |
4 | a0001c0001t0002g0060 a0001c0001t0002g0109 a0001c0001t0002g0110 others(1): Show |
4 | HG01192.hp2 HG02148.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+1536_92+1537ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | |||||||
| chr19:4122247 | G | GACCCTCC others(203): Show |
1 | a0001c0001t0001g0173 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.92+1536_92+1537ins others(210): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | |||||||
| chr19:4122247 | G | GACCCTCC others(203): Show |
1 | a0001c0001t0001g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.92+1536_92+1537ins others(210): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | |||||||
| chr19:4122247 | G | GACCCTCC others(173): Show |
2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA18952.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.92+1536_92+1537ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | |||||||
| chr19:4122247 | G | GACCCTCC others(203): Show |
55 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0062 others(52): Show |
60 | HG00423.hp2 HG00597.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.92+1536_92+1537ins others(210): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | |||||||
| chr19:4122247 | G | GACCCTCC others(204): Show |
1 | a0001c0001t0002g0116 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.92+1536_92+1537ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | |||||||
| chr19:4122273 | T | C | 4 | a0001c0001t0001g0173 a0001c0001t0001g0274 a0001c0001t0001g0275 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.92+1511A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122273 | |||||||
| chr19:4122277 | G | A | 111 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0001g0174 others(108): Show |
118 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.92+1507C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122277 | |||||||
| chr19:4122277 | G | GACCCTCC others(23): Show |
8 | a0001c0001t0002g0229 a0001c0002t0001g0199 a0001c0002t0001g0209 others(5): Show |
8 | HG01433.hp1 HG02165.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.92+1506_92+1507ins others(30): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122277 | |||||||
| chr19:4122282 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG02970.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.92+1502A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122282 | |||||||
| chr19:4122284 | C | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG02970.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.92+1500G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122284 | |||||||
| chr19:4122303 | C | T | 22 | a0001c0005t0001g0271 a0001c0005t0003g0002 a0001c0005t0003g0042 others(19): Show |
25 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.92+1481G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122303 | |||||||
| chr19:4122307 | G | A | 7 | a0001c0006t0001g0273 a0001c0006t0001g0279 a0001c0006t0004g0297 others(4): Show |
7 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.92+1477C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122307 | |||||||
| chr19:4122308 | A | AC | 10 | a0001c0001t0001g0074 a0001c0001t0002g0047 a0001c0001t0002g0048 others(7): Show |
10 | HG01175.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+1475dupG | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122308 | |||||||
| chr19:4122308 | A | ACCCCCCT others(207): Show |
1 | a0001c0001t0001g0056 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.92+1475_92+1476ins others(214): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122308 | |||||||
| chr19:4122308 | A | ACCCCCTC others(205): Show |
1 | a0001c0001t0001g0043 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.92+1475_92+1476ins others(212): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122308 | |||||||
| chr19:4122308 | A | ACCCCCTC others(204): Show |
1 | a0001c0001t0001g0073 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.92+1475_92+1476ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122308 | |||||||
| chr19:4122312 | C | T | 22 | a0001c0005t0001g0271 a0001c0005t0003g0002 a0001c0005t0003g0042 others(19): Show |
25 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.92+1472G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122312 | |||||||
| chr19:4122314 | T | C | 22 | a0001c0005t0001g0271 a0001c0005t0003g0002 a0001c0005t0003g0042 others(19): Show |
25 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.92+1470A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122314 | |||||||
| chr19:4122333 | T | C | 15 | a0001c0001t0001g0036 a0001c0001t0003g0057 a0001c0001t0005g0283 others(12): Show |
15 | HG01099.hp2 HG01109.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.92+1451A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122333 | |||||||
| chr19:4122333 | T | TAGGGACC others(23): Show |
14 | a0001c0005t0001g0271 a0001c0005t0003g0002 a0001c0005t0003g0042 others(11): Show |
17 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.92+1450_92+1451ins others(30): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122333 | |||||||
| chr19:4122338 | A | AC | 20 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0061 others(17): Show |
20 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.92+1445dupG | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122338 | |||||||
| chr19:4122338 | A | ACCCCCTC others(205): Show |
1 | a0001c0001t0003g0057 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.92+1445_92+1446ins others(212): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122338 | |||||||
| chr19:4122338 | A | ACCCCCTC others(204): Show |
3 | a0001c0001t0001g0036 a0001c0003t0001g0058 a0001c0003t0001g0059 |
3 | HG01123.hp1 HG02615.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.92+1445_92+1446ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122338 | |||||||
| chr19:4122338 | A | ACCCCCTC others(205): Show |
1 | a0001c0002t0007g0284 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.92+1445_92+1446ins others(212): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122338 | |||||||
| chr19:4122338 | A | ACCCTCCC others(24): Show |
1 | a0001c0005t0003g0072 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.92+1445_92+1446ins others(31): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122338 | |||||||
| chr19:4122342 | C | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG02970.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.92+1442G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122342 | |||||||
| chr19:4122344 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG02970.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.92+1440A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122344 | |||||||
| chr19:4122363 | T | C | 1 | a0001c0001t0005g0283 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.92+1421A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122363 | |||||||
| chr19:4122367 | G | GACCCTCC others(83): Show |
2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG02970.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.92+1416_92+1417ins others(90): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122367 | |||||||
| chr19:4122398 | A | AC | 15 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0002g0034 others(12): Show |
15 | HG01099.hp1 HG01175.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.92+1385dupG | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122398 | |||||||
| chr19:4122398 | A | ACCCTCCC others(205): Show |
1 | a0001c0001t0005g0283 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.92+1385_92+1386ins others(212): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122398 | |||||||
| chr19:4122458 | A | AC | 12 | a0001c0001t0001g0036 a0001c0001t0002g0034 a0001c0001t0003g0035 others(9): Show |
12 | HG01175.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.92+1325dupG | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122458 | |||||||
| chr19:4122677 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.92+1107G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122677 | |||||||
| chr19:4122741 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.92+1043G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122741 | |||||||
| chr19:4122764 | G | A | 1 | a0001c0002t0001g0276 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92+1020C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122764 | |||||||
| chr19:4122812 | G | C | 15 | a0001c0001t0003g0277 a0001c0001t0004g0300 a0001c0001t0004g0301 others(12): Show |
15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.92+972C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122812 | |||||||
| chr19:4122879 | T | C | 309 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(306): Show |
325 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.92+905A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122879 | |||||||
| chr19:4123050 | T | TCCCTACT others(9): Show |
1 | a0001c0001t0001g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+718_92+733dupGA others(14): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123050 | |||||||
| chr19:4123091 | G | A | 2 | a0001c0006t0001g0279 a0001c0006t0008g0314 |
2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.92+693C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123091 | |||||||
| chr19:4123166 | T | C | 1 | a0001c0003t0005g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.92+618A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123166 | |||||||
| chr19:4123398 | C | T | 1 | a0001c0001t0005g0283 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.92+386G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123398 | |||||||
| chr19:4123514 | CCCCCCTG others(111): Show |
C | 1 | a0001c0001t0002g0026 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.92+152_92+269del | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123514 | |||||||
| chr19:4123518 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.92+266G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123518 | |||||||
| chr19:4123542 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92+242C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123542 | |||||||
| chr19:4123542 | G | GTCCTCCG others(19): Show |
1 | a0001c0002t0002g0252 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.92+216_92+241dupGG others(24): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123542 | |||||||
| chr19:4123546 | TCCGAGGG others(19): Show |
T | 60 | a0001c0001t0001g0056 a0001c0001t0001g0073 a0001c0001t0001g0078 others(57): Show |
61 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.92+212_92+237delGG others(24): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123546 | |||||||
| chr19:4123554 | C | CCCCCTGC others(19): Show |
78 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0033 others(75): Show |
85 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.92+229_92+230insAC others(24): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123554 | |||||||
| chr19:4123554 | C | CCCCCTGC others(97): Show |
1 | a0001c0002t0003g0186 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.92+229_92+230insAC others(102): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123554 | |||||||
| chr19:4123554 | C | CCCCCTGC others(123): Show |
7 | a0001c0001t0001g0188 a0001c0001t0003g0190 a0001c0002t0003g0183 others(4): Show |
7 | HG01884.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.92+229_92+230insAC others(128): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123554 | |||||||
| chr19:4123554 | C | CCCCCTGC others(45): Show |
4 | a0001c0001t0001g0240 a0001c0002t0001g0211 a0001c0002t0001g0221 others(1): Show |
4 | HG00609.hp2 HG01074.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.92+229_92+230insAC others(50): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123554 | |||||||
| chr19:4123554 | C | CCCCCTGC others(111): Show |
2 | a0001c0001t0001g0174 a0001c0004t0006g0196 |
2 | HG02109.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.92+229_92+230insAC others(116): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123554 | |||||||
| chr19:4123564 | C | CGTCCTCC others(71): Show |
1 | a0001c0001t0002g0051 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.92+219_92+220insAG others(76): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123564 | |||||||
| chr19:4123564 | C | CGTCCTCC others(45): Show |
1 | a0001c0002t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.92+168_92+219dupAG others(50): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123564 | |||||||
| chr19:4123572 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0099 |
2 | HG00738.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.92+212G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123572 | |||||||
| chr19:4123579 | G | GTCCCCTG others(124): Show |
1 | a0001c0001t0003g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.92+204_92+205insGC others(129): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123579 | |||||||
| chr19:4123580 | C | T | 38 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0032 others(35): Show |
39 | HG00639.hp2 HG00735.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.92+204G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123580 | |||||||
| chr19:4123591 | G | A | 2 | a0001c0001t0001g0016 a0001c0002t0001g0015 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.92+193C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123591 | |||||||
| chr19:4123598 | C | T | 2 | a0001c0001t0001g0016 a0001c0002t0001g0015 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.92+186G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123598 | |||||||
| chr19:4123599 | C | T | 2 | a0001c0001t0001g0016 a0001c0002t0001g0015 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.92+185G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123599 | |||||||
| chr19:4123603 | G | A | 2 | a0001c0001t0001g0016 a0001c0002t0001g0015 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.92+181C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123603 | |||||||
| chr19:4123605 | GTCCCCTG others(20): Show |
G | 18 | a0001c0001t0001g0105 a0001c0001t0001g0132 a0001c0001t0003g0277 others(15): Show |
18 | HG01358.hp2 HG02723.hp2 HG02735.hp2 others(15): Show |
intron_variant | MODIFIER | c.92+152_92+178delTT others(25): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123605 | |||||||
| chr19:4123606 | T | C | 4 | a0001c0001t0001g0016 a0001c0002t0001g0015 a0001c0002t0001g0017 others(1): Show |
4 | HG00639.hp2 HG00735.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+178A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123606 | |||||||
| chr19:4123611 | T | TGAACCTC others(37): Show |
3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0002t0001g0014 |
3 | HG02976.hp2 NA19091.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.92+172_92+173insGA others(42): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123611 | |||||||
| chr19:4123616 | T | C | 57 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(54): Show |
58 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.92+168A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123616 | |||||||
| chr19:4123617 | G | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(3): Show |
6 | HG00639.hp2 HG00735.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+167C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123617 | |||||||
| chr19:4123617 | G | GTCCTCCC others(141): Show |
1 | a0001c0002t0001g0018 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.92+166_92+167insTG others(146): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123617 | |||||||
| chr19:4123617 | G | GTCCTCCC others(89): Show |
1 | a0001c0002t0001g0017 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.92+166_92+167insTG others(94): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123617 | |||||||
| chr19:4123659 | C | T | 4 | a0001c0006t0001g0022 a0001c0006t0001g0023 a0001c0006t0001g0024 others(1): Show |
4 | HG00408.hp2 NA18747.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+125G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123659 | |||||||
| chr19:4123677 | C | T | 10 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+107G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123677 | |||||||
| chr19:4123732 | G | A | 1 | a0001c0002t0002g0280 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.92+52C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123732 | |||||||
| chr19:4123742 | C | A | 1 | a0001c0001t0001g0281 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.92+42G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123742 |