Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6416 |
| ensemblid | ENSG00000065559.15 |
| hgncid | 6844 |
| symbol | MAP2K4 |
| name | mitogen-activated protein kinase kinase 4 |
| refseq_nuc | NM_003010.4 |
| refseq_prot | NP_003001.1 |
| ensembl_nuc | ENST00000353533.10 |
| ensembl_prot | ENSP00000262445.5 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 12020877 |
| end | 12143828 |
| strand | + |
| ver | v1.2 |
| region | chr17:12020877-12143828 |
| region5000 | chr17:12015877-12148828 |
| regionname0 | MAP2K4_chr17_12020877_12143828 |
| regionname5000 | MAP2K4_chr17_12015877_12148828 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 399 | 321 | 90 | 45 | 140 | 12 | 32 | 102 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | MAAPS others(394): Show |
chr17 | 12015877 | 12148828 |
| a0002 | 0/0 | 399 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | MAAPS others(394): Show |
chr17 | 12015877 | 12148828 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1197 | 317 | 88 | 45 | 138 | 12 | 32 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ATGGC others(1192): Show |
chr17 | 12015877 | 12148828 | ||
| a0001c0002 | 0/0 | 1197 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ATGGC others(1192): Show |
chr17 | 12015877 | 12148828 | ||
| a0001c0003 | 0/0 | 1197 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ATGGC others(1192): Show |
chr17 | 12015877 | 12148828 | ||
| a0002c0004 | 0/0 | 1197 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ATGGC others(1192): Show |
chr17 | 12015877 | 12148828 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3778 | 197 | 73 | 28 | 65 | 10 | 20 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0002 | 0/0 | 3778 | 60 | 7 | 14 | 28 | 1 | 10 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0003 | 0/0 | 3778 | 16 | 0 | 0 | 16 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0004 | 0/0 | 3779 | 18 | 3 | 0 | 15 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3774): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0005 | 0/0 | 3778 | 5 | 0 | 0 | 5 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0006 | 0/0 | 3778 | 4 | 0 | 0 | 4 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0007 | 0/0 | 3778 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0008 | 0/0 | 3778 | 3 | 0 | 0 | 3 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0009 | 0/0 | 3778 | 2 | 0 | 0 | 0 | 0 | 2 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0010 | 0/1 | 3778 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0011 | 0/0 | 3778 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0013 | 0/0 | 3778 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0014 | 0/0 | 3778 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0015 | 0/0 | 3778 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0016 | 0/0 | 3778 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0017 | 0/0 | 3778 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0018 | 0/0 | 3778 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0001t0019 | 0/0 | 3778 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0002t0003 | 0/0 | 3778 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0003t0001 | 0/0 | 3778 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0001c0003t0002 | 0/0 | 3778 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| a0002c0004t0012 | 0/0 | 3778 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | ACTCC others(3773): Show |
chr17 | 12015877 | 12148828 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0008g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0009g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0010g0253 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0011g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0013g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0014g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0015g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0016g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0017g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0018g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0019g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0003t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0002c0004t0012g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | GBR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | GBR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0293 | EUR | FIN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0051 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00609 | hp2 | a0001 | c0001 | t0006 | g0094 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0307 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01243 | hp1 | a0001 | c0001 | t0013 | g0005 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01243 | hp2 | a0002 | c0004 | t0012 | g0027 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0319 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | IBS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0197 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02145 | hp2 | a0001 | c0001 | t0011 | g0017 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | CDX | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CDX | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CDX | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02273 | hp1 | a0001 | c0001 | t0015 | g0216 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02273 | hp2 | a0001 | c0001 | t0016 | g0234 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0280 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0249 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0318 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03490 | hp1 | a0001 | c0001 | t0009 | g0001 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03492 | hp2 | a0001 | c0001 | t0009 | g0001 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0275 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | BEB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | STU | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | STU | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | STU | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | STU | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18612 | hp1 | a0001 | c0002 | t0003 | g0084 | EAS | CHB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | CHB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | CHB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | YRI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18906 | hp2 | a0001 | c0001 | t0018 | g0046 | AFR | YRI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18967 | hp2 | a0001 | c0001 | t0006 | g0111 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18990 | hp1 | a0001 | c0001 | t0008 | g0191 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18992 | hp1 | a0001 | c0001 | t0019 | g0295 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18997 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | LWK | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0223 | AFR | LWK | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | LWK | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19054 | hp2 | a0001 | c0001 | t0008 | g0192 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19060 | hp1 | a0001 | c0001 | t0006 | g0115 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19066 | hp2 | a0001 | c0001 | t0006 | g0126 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19075 | hp1 | a0001 | c0001 | t0014 | g0090 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19084 | hp2 | a0001 | c0001 | t0008 | g0189 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ASW | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ASW | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20752 | hp1 | a0001 | c0001 | t0017 | g0077 | EUR | TSI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | TSI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0271 | EUR | TSI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0279 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0248 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | USA | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | USA | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | USA | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | USA | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0010 | g0253 | REF | REF | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0160 | REF | REF | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:12054976 | T | C | 1 | a0002 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.203T>C | p.Val68Ala | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/11 | 213/3778 | 203/1200 | 68/399 | chr17 | 12054976 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:12020949 | C | T | 1 | a0001c0003 | 2 | HG02559.hp1 HG02572.hp1 |
synonymous_variant | LOW | c.63C>T | p.Pro21Pro | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/11 | 73/3778 | 63/1200 | 21/399 | chr17 | 12020949 | |||
| chr17:12139845 | G | A | 1 | a0001c0002 | 2 | HG00597.hp2 NA18612.hp1 |
synonymous_variant | LOW | c.1047G>A | p.Thr349Thr | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/11 | 1057/3778 | 1047/1200 | 349/399 | chr17 | 12139845 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:12141709 | A | G | 1 | a0001c0001t0008 | 3 | NA18990.hp1 NA19054.hp2 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*449A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 449 | chr17 | 12141709 | ||||||
| chr17:12141976 | A | G | 1 | a0001c0001t0006 | 4 | HG00609.hp2 NA18967.hp2 NA19060.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*716A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 716 | chr17 | 12141976 | ||||||
| chr17:12141985 | T | TG | 1 | a0001c0001t0004 | 18 | HG00673.hp2 HG01891.hp2 HG02040.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*728dupG | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 729 | INFO_REALIGN_3_PRIME | chr17 | 12141985 | |||||
| chr17:12142026 | G | C | 1 | a0001c0001t0011 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*766G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 766 | chr17 | 12142026 | ||||||
| chr17:12142057 | G | A | 1 | a0001c0001t0005 | 5 | HG00673.hp1 HG02083.hp2 NA18950.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*797G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 797 | chr17 | 12142057 | ||||||
| chr17:12142214 | C | G | 1 | a0001c0001t0019 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*954C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 954 | chr17 | 12142214 | ||||||
| chr17:12142359 | G | A | 1 | a0002c0004t0012 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1099G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 1099 | chr17 | 12142359 | ||||||
| chr17:12142434 | A | G | 1 | a0001c0001t0018 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1174A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 1174 | chr17 | 12142434 | ||||||
| chr17:12142446 | C | T | 1 | a0001c0001t0017 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1186C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 1186 | chr17 | 12142446 | ||||||
| chr17:12142588 | G | A | 3 | a0001c0001t0002 a0001c0001t0019 a0001c0003t0002 |
62 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1328G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 1328 | chr17 | 12142588 | ||||||
| chr17:12142692 | A | G | 1 | a0001c0001t0007 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1432A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 1432 | chr17 | 12142692 | ||||||
| chr17:12142857 | A | G | 1 | a0001c0001t0009 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1597A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 1597 | chr17 | 12142857 | ||||||
| chr17:12142989 | T | C | 1 | a0001c0001t0013 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1729T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 1729 | chr17 | 12142989 | ||||||
| chr17:12143300 | C | G | 1 | a0001c0001t0016 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2040C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 2040 | chr17 | 12143300 | ||||||
| chr17:12143355 | A | G | 1 | a0001c0001t0015 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2095A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 2095 | chr17 | 12143355 | ||||||
| chr17:12143574 | A | G | 2 | a0001c0001t0003 a0001c0002t0003 |
18 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2314A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 2314 | chr17 | 12143574 | ||||||
| chr17:12143635 | T | C | 1 | a0001c0001t0014 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2375T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 2375 | chr17 | 12143635 | ||||||
| chr17:12143663 | C | T | 1 | a0002c0004t0012 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2403C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 2403 | chr17 | 12143663 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:12021118 | T | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.115+117T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021118 | |||||||
| chr17:12021154 | C | T | 66 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(63): Show |
66 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.115+153C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021154 | |||||||
| chr17:12021167 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.115+166G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021167 | |||||||
| chr17:12021278 | T | C | 1 | a0001c0001t0007g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+277T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021278 | |||||||
| chr17:12021285 | C | G | 2 | a0001c0001t0002g0251 a0001c0001t0002g0252 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.115+284C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021285 | |||||||
| chr17:12021322 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.115+321C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021322 | |||||||
| chr17:12021370 | T | C | 1 | a0001c0001t0004g0026 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.115+369T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021370 | |||||||
| chr17:12021407 | G | A | 2 | a0001c0001t0007g0025 a0002c0004t0012g0027 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.115+406G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021407 | |||||||
| chr17:12021619 | G | T | 2 | a0001c0001t0007g0248 a0001c0001t0007g0249 |
2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.115+618G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021619 | |||||||
| chr17:12021708 | T | A | 1 | a0001c0001t0007g0248 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.115+707T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021708 | |||||||
| chr17:12021734 | G | GA | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0024 others(132): Show |
138 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.115+754dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12021734 | ||||||
| chr17:12021734 | G | GAA | 7 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0256 others(4): Show |
7 | HG01884.hp1 HG02027.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.115+753_115+754dup others(2): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12021734 | ||||||
| chr17:12021734 | GA | G | 7 | a0001c0001t0001g0023 a0001c0001t0001g0239 a0001c0001t0001g0240 others(4): Show |
7 | HG01256.hp2 HG02818.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+754delA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12021734 | ||||||
| chr17:12021753 | A | G | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+752A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021753 | |||||||
| chr17:12021841 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG01934.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.115+840C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021841 | |||||||
| chr17:12022019 | T | C | 16 | a0001c0001t0002g0257 a0001c0001t0002g0258 a0001c0001t0002g0259 others(13): Show |
16 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.115+1018T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022019 | |||||||
| chr17:12022275 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.115+1274A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022275 | |||||||
| chr17:12022725 | T | C | 1 | a0001c0001t0003g0031 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.115+1724T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022725 | |||||||
| chr17:12022737 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.115+1736G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022737 | |||||||
| chr17:12022796 | G | C | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | NA18747.hp2 NA18955.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.115+1795G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022796 | |||||||
| chr17:12022834 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.115+1833A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022834 | |||||||
| chr17:12022871 | C | T | 1 | a0001c0001t0002g0315 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.115+1870C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022871 | |||||||
| chr17:12022893 | C | G | 2 | a0001c0001t0007g0248 a0001c0001t0007g0249 |
2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.115+1892C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022893 | |||||||
| chr17:12023266 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.115+2265G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023266 | |||||||
| chr17:12023296 | T | G | 1 | a0001c0001t0001g0028 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.115+2295T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023296 | |||||||
| chr17:12023516 | C | G | 19 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.115+2515C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023516 | |||||||
| chr17:12023521 | C | G | 2 | a0001c0001t0001g0235 a0001c0001t0016g0234 |
2 | HG00639.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.115+2520C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023521 | |||||||
| chr17:12023620 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.115+2619G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023620 | |||||||
| chr17:12023719 | A | G | 2 | a0001c0001t0007g0025 a0002c0004t0012g0027 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.115+2718A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023719 | |||||||
| chr17:12023785 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0239 |
2 | HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.115+2784G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023785 | |||||||
| chr17:12023848 | G | A | 2 | a0001c0001t0007g0025 a0002c0004t0012g0027 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.115+2847G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023848 | |||||||
| chr17:12023857 | G | C | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.115+2856G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023857 | |||||||
| chr17:12023997 | A | C | 1 | a0001c0001t0001g0314 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.115+2996A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023997 | |||||||
| chr17:12024140 | A | G | 62 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(59): Show |
65 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.115+3139A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12024140 | |||||||
| chr17:12024318 | C | T | 60 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(57): Show |
63 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.115+3317C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12024318 | |||||||
| chr17:12024421 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.115+3420A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12024421 | |||||||
| chr17:12024448 | A | G | 1 | a0001c0001t0002g0313 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.115+3447A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12024448 | |||||||
| chr17:12024449 | T | C | 2 | a0001c0001t0007g0025 a0002c0004t0012g0027 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.115+3448T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12024449 | |||||||
| chr17:12024748 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.115+3747G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12024748 | |||||||
| chr17:12024977 | G | T | 37 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0288 others(34): Show |
37 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.115+3976G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12024977 | |||||||
| chr17:12025018 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.115+4017A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12025018 | |||||||
| chr17:12025231 | C | A | 2 | a0001c0001t0007g0025 a0002c0004t0012g0027 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.115+4230C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12025231 | |||||||
| chr17:12025550 | T | C | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.115+4549T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12025550 | |||||||
| chr17:12025629 | T | G | 2 | a0001c0001t0007g0025 a0002c0004t0012g0027 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.115+4628T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12025629 | |||||||
| chr17:12025712 | G | A | 41 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(38): Show |
41 | HG00280.hp1 HG00558.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.115+4711G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12025712 | |||||||
| chr17:12025870 | CTAAT | C | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 |
3 | HG01106.hp2 HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.115+4872_115+4875d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12025870 | ||||||
| chr17:12026305 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.115+5304T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12026305 | |||||||
| chr17:12026408 | G | A | 6 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+5407G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12026408 | |||||||
| chr17:12026738 | G | A | 1 | a0001c0001t0007g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+5737G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12026738 | |||||||
| chr17:12026956 | T | G | 1 | a0001c0001t0007g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+5955T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12026956 | |||||||
| chr17:12027467 | A | T | 66 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(63): Show |
66 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.115+6466A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12027467 | |||||||
| chr17:12027484 | T | TAC | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.115+6497_115+6498d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12027484 | ||||||
| chr17:12027664 | T | G | 16 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(13): Show |
16 | HG00673.hp2 HG00733.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.115+6663T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12027664 | |||||||
| chr17:12027777 | G | A | 2 | a0001c0001t0002g0285 a0001c0001t0002g0286 |
2 | NA18986.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.115+6776G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12027777 | |||||||
| chr17:12027824 | A | T | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.115+6823A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12027824 | |||||||
| chr17:12028084 | A | G | 1 | a0001c0001t0007g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+7083A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12028084 | |||||||
| chr17:12028132 | A | G | 2 | a0001c0001t0002g0251 a0001c0001t0002g0252 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.115+7131A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12028132 | |||||||
| chr17:12028725 | G | C | 1 | a0001c0001t0007g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+7724G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12028725 | |||||||
| chr17:12028911 | A | G | 1 | a0001c0001t0002g0319 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.115+7910A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12028911 | |||||||
| chr17:12028922 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.115+7921A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12028922 | |||||||
| chr17:12029043 | C | T | 1 | a0001c0001t0007g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+8042C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029043 | |||||||
| chr17:12029087 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0281 a0001c0001t0001g0282 others(2): Show |
5 | HG02055.hp2 HG02647.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+8086C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029087 | |||||||
| chr17:12029173 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.115+8172G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029173 | |||||||
| chr17:12029200 | C | T | 120 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0001g0101 others(117): Show |
120 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.115+8199C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029200 | |||||||
| chr17:12029213 | T | TA | 6 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+8213dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12029213 | ||||||
| chr17:12029278 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+8277G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029278 | |||||||
| chr17:12029419 | A | C | 2 | a0001c0003t0001g0279 a0001c0003t0002g0280 |
2 | HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.115+8418A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029419 | |||||||
| chr17:12029681 | A | G | 26 | a0001c0001t0001g0256 a0001c0001t0001g0294 a0001c0001t0002g0254 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.115+8680A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029681 | |||||||
| chr17:12029732 | C | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG00733.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.115+8731C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029732 | |||||||
| chr17:12030096 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.115+9095C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12030096 | |||||||
| chr17:12030255 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.115+9254A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12030255 | |||||||
| chr17:12030315 | C | T | 5 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0242 others(2): Show |
5 | HG02083.hp1 NA18982.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.115+9314C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12030315 | |||||||
| chr17:12030336 | A | G | 66 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(63): Show |
66 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.115+9335A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12030336 | |||||||
| chr17:12030405 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.115+9404A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12030405 | |||||||
| chr17:12030563 | A | G | 1 | a0001c0001t0002g0318 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.115+9562A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12030563 | |||||||
| chr17:12030657 | A | T | 196 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0024 others(193): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.115+9656A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12030657 | |||||||
| chr17:12031024 | T | A | 2 | a0001c0001t0002g0251 a0001c0001t0002g0252 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.115+10023T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031024 | |||||||
| chr17:12031231 | T | C | 1 | a0001c0001t0001g0281 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.115+10230T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031231 | |||||||
| chr17:12031304 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.115+10303T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031304 | |||||||
| chr17:12031375 | G | A | 2 | a0001c0001t0002g0232 a0001c0001t0018g0046 |
2 | NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.115+10374G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031375 | |||||||
| chr17:12031421 | A | G | 1 | a0001c0001t0002g0227 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.115+10420A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031421 | |||||||
| chr17:12031444 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.115+10443G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031444 | |||||||
| chr17:12031533 | C | T | 2 | a0001c0001t0002g0232 a0001c0001t0018g0046 |
2 | NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.115+10532C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031533 | |||||||
| chr17:12031701 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.115+10700C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031701 | |||||||
| chr17:12031709 | T | C | 6 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(3): Show |
6 | HG01071.hp2 HG01346.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+10708T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031709 | |||||||
| chr17:12031728 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.115+10727G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031728 | |||||||
| chr17:12031800 | T | C | 6 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+10799T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031800 | |||||||
| chr17:12032579 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.115+11578A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12032579 | |||||||
| chr17:12032604 | A | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0100 a0001c0001t0001g0176 others(1): Show |
4 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+11603A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12032604 | |||||||
| chr17:12032715 | A | C | 13 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(10): Show |
13 | HG02040.hp2 HG02818.hp1 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.115+11714A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12032715 | |||||||
| chr17:12032975 | G | A | 1 | a0001c0001t0007g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+11974G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12032975 | |||||||
| chr17:12033196 | A | G | 1 | a0001c0001t0002g0312 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.115+12195A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12033196 | |||||||
| chr17:12033337 | C | CA | 66 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(63): Show |
66 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.115+12344dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12033337 | ||||||
| chr17:12033513 | A | G | 13 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(10): Show |
13 | HG02040.hp2 HG02818.hp1 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.115+12512A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12033513 | |||||||
| chr17:12033635 | T | C | 1 | a0001c0001t0002g0258 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.115+12634T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12033635 | |||||||
| chr17:12033815 | T | C | 1 | a0001c0001t0007g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+12814T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12033815 | |||||||
| chr17:12033831 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.115+12830G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12033831 | |||||||
| chr17:12033961 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.115+12960A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12033961 | |||||||
| chr17:12034128 | C | A | 28 | a0001c0001t0001g0045 a0001c0001t0001g0104 a0001c0001t0001g0178 others(25): Show |
28 | HG00099.hp1 HG01071.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.115+13127C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034128 | |||||||
| chr17:12034256 | C | T | 1 | a0001c0001t0007g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+13255C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034256 | |||||||
| chr17:12034358 | A | G | 4 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG02055.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+13357A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034358 | |||||||
| chr17:12034593 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0100 a0001c0001t0001g0176 others(1): Show |
4 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+13592C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034593 | |||||||
| chr17:12034614 | G | T | 1 | a0001c0001t0004g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.115+13613G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034614 | |||||||
| chr17:12034641 | A | G | 1 | a0001c0001t0007g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+13640A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034641 | |||||||
| chr17:12034770 | T | G | 1 | a0001c0001t0007g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+13769T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034770 | |||||||
| chr17:12034790 | C | T | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.115+13789C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034790 | |||||||
| chr17:12034978 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.115+13977G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034978 | |||||||
| chr17:12035227 | T | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0100 a0001c0001t0001g0176 others(1): Show |
4 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+14226T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12035227 | |||||||
| chr17:12035243 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.115+14242C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12035243 | |||||||
| chr17:12035246 | G | A | 6 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+14245G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12035246 | |||||||
| chr17:12035377 | C | T | 2 | a0001c0001t0007g0248 a0001c0001t0007g0249 |
2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.115+14376C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12035377 | |||||||
| chr17:12035469 | T | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(55): Show |
61 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.115+14468T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12035469 | |||||||
| chr17:12035511 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0241 |
2 | NA19010.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.115+14510C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12035511 | |||||||
| chr17:12036346 | A | T | 1 | a0001c0001t0001g0226 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.115+15345A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12036346 | |||||||
| chr17:12036564 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.115+15563C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12036564 | |||||||
| chr17:12036676 | T | A | 1 | a0001c0001t0002g0232 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.115+15675T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12036676 | |||||||
| chr17:12036706 | AT | A | 122 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0095 others(119): Show |
122 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.115+15718delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12036706 | ||||||
| chr17:12036903 | C | CT | 134 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(131): Show |
134 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.115+15910dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12036903 | ||||||
| chr17:12036979 | A | G | 1 | a0001c0001t0007g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+15978A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12036979 | |||||||
| chr17:12037251 | G | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0093 |
4 | NA18955.hp1 NA18984.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+16250G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12037251 | |||||||
| chr17:12037572 | A | G | 17 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(14): Show |
17 | HG02040.hp2 HG02818.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.115+16571A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12037572 | |||||||
| chr17:12037630 | T | TTA | 121 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(118): Show |
121 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.115+16638_115+1663 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12037630 | ||||||
| chr17:12037705 | A | G | 1 | a0001c0001t0007g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+16704A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12037705 | |||||||
| chr17:12037843 | C | G | 6 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+16842C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12037843 | |||||||
| chr17:12037916 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.115+16915G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12037916 | |||||||
| chr17:12038166 | C | T | 121 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(118): Show |
121 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.116-16723C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038166 | |||||||
| chr17:12038177 | A | T | 121 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(118): Show |
121 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.116-16712A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038177 | |||||||
| chr17:12038358 | T | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(62): Show |
68 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.116-16531T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038358 | |||||||
| chr17:12038396 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.116-16493G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038396 | |||||||
| chr17:12038421 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.116-16468C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038421 | |||||||
| chr17:12038462 | G | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0140 |
2 | NA18945.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.116-16427G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038462 | |||||||
| chr17:12038586 | A | T | 1 | a0001c0001t0001g0203 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.116-16303A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038586 | |||||||
| chr17:12038756 | A | G | 1 | a0001c0001t0004g0155 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.116-16133A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038756 | |||||||
| chr17:12039095 | G | A | 6 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-15794G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12039095 | |||||||
| chr17:12039218 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.116-15671A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12039218 | |||||||
| chr17:12039521 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.116-15368A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12039521 | |||||||
| chr17:12039567 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.116-15322A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12039567 | |||||||
| chr17:12039622 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.116-15267A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12039622 | |||||||
| chr17:12039671 | A | G | 11 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(8): Show |
11 | HG01934.hp1 HG02145.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.116-15218A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12039671 | |||||||
| chr17:12040004 | C | T | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.116-14885C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12040004 | |||||||
| chr17:12040144 | C | T | 6 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
6 | NA18967.hp1 NA19002.hp2 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-14745C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12040144 | |||||||
| chr17:12040294 | GC | G | 66 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(63): Show |
66 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.116-14594delC | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12040294 | |||||||
| chr17:12040384 | C | T | 23 | a0001c0001t0001g0095 a0001c0001t0001g0105 a0001c0001t0001g0205 others(20): Show |
23 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.116-14505C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12040384 | |||||||
| chr17:12040423 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.116-14466A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12040423 | |||||||
| chr17:12040802 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.116-14087T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12040802 | |||||||
| chr17:12040949 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18747.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.116-13940T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12040949 | |||||||
| chr17:12041173 | A | G | 8 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(5): Show |
8 | HG02451.hp2 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-13716A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12041173 | |||||||
| chr17:12041656 | G | GA | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.116-13225dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12041656 | ||||||
| chr17:12041828 | A | AAAGAACT others(6): Show |
1 | a0001c0001t0001g0034 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.116-13060_116-1304 others(17): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12041828 | ||||||
| chr17:12041906 | C | T | 96 | a0001c0001t0001g0045 a0001c0001t0001g0101 a0001c0001t0001g0102 others(93): Show |
96 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.116-12983C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12041906 | |||||||
| chr17:12042048 | G | A | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.116-12841G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042048 | |||||||
| chr17:12042167 | C | CA | 85 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0034 others(82): Show |
85 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.116-12699dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12042167 | ||||||
| chr17:12042167 | C | CAA | 122 | a0001c0001t0001g0030 a0001c0001t0001g0045 a0001c0001t0001g0048 others(119): Show |
122 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.116-12700_116-1269 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12042167 | ||||||
| chr17:12042167 | C | CAAA | 51 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(48): Show |
54 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.116-12701_116-1269 others(7): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12042167 | ||||||
| chr17:12042167 | C | CAAAA | 9 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(6): Show |
9 | HG00597.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.116-12702_116-1269 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12042167 | ||||||
| chr17:12042226 | C | T | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.116-12663C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042226 | |||||||
| chr17:12042330 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.116-12559T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042330 | |||||||
| chr17:12042465 | G | T | 58 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(55): Show |
61 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.116-12424G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042465 | |||||||
| chr17:12042579 | C | T | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.116-12310C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042579 | |||||||
| chr17:12042580 | G | A | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.116-12309G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042580 | |||||||
| chr17:12042643 | A | AAAAC | 265 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(262): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.116-12234_116-1223 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12042643 | ||||||
| chr17:12042659 | A | T | 1 | a0001c0001t0001g0034 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.116-12230A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042659 | |||||||
| chr17:12042852 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.116-12037C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042852 | |||||||
| chr17:12043189 | A | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(55): Show |
61 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.116-11700A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043189 | |||||||
| chr17:12043193 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.116-11696C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043193 | |||||||
| chr17:12043239 | T | G | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(1): Show |
4 | HG02145.hp1 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-11650T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043239 | |||||||
| chr17:12043277 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.116-11612A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043277 | |||||||
| chr17:12043315 | A | C | 129 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(126): Show |
129 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.116-11574A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043315 | |||||||
| chr17:12043442 | T | G | 1 | a0001c0001t0001g0034 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.116-11447T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043442 | |||||||
| chr17:12043448 | G | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0239 |
2 | HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.116-11441G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043448 | |||||||
| chr17:12043609 | G | A | 1 | a0001c0001t0002g0106 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.116-11280G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043609 | |||||||
| chr17:12043757 | T | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(55): Show |
61 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.116-11132T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043757 | |||||||
| chr17:12043919 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0100 |
2 | HG01192.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.116-10970G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043919 | |||||||
| chr17:12044061 | C | G | 64 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(61): Show |
67 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.116-10828C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12044061 | |||||||
| chr17:12044293 | G | A | 6 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-10596G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12044293 | |||||||
| chr17:12044386 | A | G | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.116-10503A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12044386 | |||||||
| chr17:12044616 | T | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.116-10273T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12044616 | |||||||
| chr17:12044826 | T | G | 1 | a0001c0001t0002g0260 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.116-10063T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12044826 | |||||||
| chr17:12044829 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.116-10060C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12044829 | |||||||
| chr17:12045357 | ATGTGATG others(7): Show |
A | 1 | a0001c0001t0007g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.116-9527_116-9514d others(16): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12045357 | ||||||
| chr17:12045581 | T | A | 1 | a0001c0001t0002g0107 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.116-9308T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12045581 | |||||||
| chr17:12045644 | T | G | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(289): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.116-9245T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12045644 | |||||||
| chr17:12045808 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.116-9081A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12045808 | |||||||
| chr17:12045910 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.116-8979G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12045910 | |||||||
| chr17:12046119 | T | A | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(289): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.116-8770T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046119 | |||||||
| chr17:12046158 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.116-8731G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046158 | |||||||
| chr17:12046335 | G | A | 1 | a0001c0001t0002g0261 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.116-8554G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046335 | |||||||
| chr17:12046344 | C | T | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.116-8545C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046344 | |||||||
| chr17:12046440 | T | A | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.116-8449T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046440 | |||||||
| chr17:12046497 | A | T | 1 | a0001c0001t0001g0034 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.116-8392A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046497 | |||||||
| chr17:12046672 | T | C | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.116-8217T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046672 | |||||||
| chr17:12046899 | C | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.116-7990C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046899 | |||||||
| chr17:12046960 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.116-7929G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046960 | |||||||
| chr17:12047017 | T | C | 6 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-7872T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047017 | |||||||
| chr17:12047061 | G | A | 64 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(61): Show |
67 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.116-7828G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047061 | |||||||
| chr17:12047063 | C | T | 1 | a0001c0001t0002g0311 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.116-7826C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047063 | |||||||
| chr17:12047065 | C | T | 297 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(294): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.116-7824C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047065 | |||||||
| chr17:12047112 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.116-7777G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047112 | |||||||
| chr17:12047137 | C | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(55): Show |
61 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.116-7752C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047137 | |||||||
| chr17:12047183 | T | C | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(289): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.116-7706T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047183 | |||||||
| chr17:12047267 | T | C | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.116-7622T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047267 | |||||||
| chr17:12047606 | A | G | 1 | a0001c0001t0001g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.116-7283A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047606 | |||||||
| chr17:12047726 | T | C | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.116-7163T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047726 | |||||||
| chr17:12047831 | TTATCACA others(4): Show |
T | 1 | a0001c0001t0001g0034 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.116-7055_116-7045d others(13): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12047831 | ||||||
| chr17:12048105 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG00733.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.116-6784C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048105 | |||||||
| chr17:12048445 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.116-6444A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048445 | |||||||
| chr17:12048497 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.116-6392T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048497 | |||||||
| chr17:12048545 | G | C | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.116-6344G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048545 | |||||||
| chr17:12048671 | T | G | 1 | a0001c0001t0002g0262 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.116-6218T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048671 | |||||||
| chr17:12048678 | C | T | 61 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(58): Show |
64 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.116-6211C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048678 | |||||||
| chr17:12048692 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.116-6197T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048692 | |||||||
| chr17:12048894 | T | G | 1 | a0001c0001t0001g0050 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.116-5995T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048894 | |||||||
| chr17:12048998 | C | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(51): Show |
57 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.116-5891C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048998 | |||||||
| chr17:12049084 | A | G | 5 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | NA18967.hp1 NA19002.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-5805A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12049084 | |||||||
| chr17:12049124 | C | G | 4 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG02055.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-5765C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12049124 | |||||||
| chr17:12049150 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.116-5739A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12049150 | |||||||
| chr17:12049444 | T | G | 1 | a0001c0001t0001g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.116-5445T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12049444 | |||||||
| chr17:12049553 | A | G | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.116-5336A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12049553 | |||||||
| chr17:12049639 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.116-5250A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12049639 | |||||||
| chr17:12049791 | A | G | 6 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-5098A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12049791 | |||||||
| chr17:12050146 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.116-4743C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12050146 | |||||||
| chr17:12050190 | G | A | 197 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(194): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.116-4699G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12050190 | |||||||
| chr17:12050586 | TGTATTGA others(15): Show |
T | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-4302_116-4281d others(24): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12050586 | |||||||
| chr17:12050609 | C | T | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-4280C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12050609 | |||||||
| chr17:12050623 | GT | G | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-4261delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12050623 | ||||||
| chr17:12050744 | T | C | 1 | a0001c0001t0014g0090 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.116-4145T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12050744 | |||||||
| chr17:12050918 | C | G | 1 | a0001c0001t0001g0128 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.116-3971C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12050918 | |||||||
| chr17:12050971 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.116-3918G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12050971 | |||||||
| chr17:12051120 | C | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0157 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.116-3769C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051120 | |||||||
| chr17:12051313 | A | G | 6 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-3576A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051313 | |||||||
| chr17:12051515 | A | G | 6 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
6 | NA18967.hp1 NA19002.hp2 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-3374A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051515 | |||||||
| chr17:12051518 | T | G | 1 | a0001c0001t0001g0314 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.116-3371T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051518 | |||||||
| chr17:12051602 | G | C | 2 | a0001c0003t0001g0279 a0001c0003t0002g0280 |
2 | HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.116-3287G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051602 | |||||||
| chr17:12051908 | G | A | 1 | a0001c0001t0009g0001 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.116-2981G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051908 | |||||||
| chr17:12051925 | T | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0100 a0001c0001t0001g0156 others(2): Show |
5 | HG01192.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-2964T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051925 | |||||||
| chr17:12051926 | A | T | 1 | a0001c0001t0002g0310 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.116-2963A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051926 | |||||||
| chr17:12051983 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.116-2906A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051983 | |||||||
| chr17:12052215 | C | G | 8 | a0001c0001t0002g0255 a0001c0001t0002g0303 a0001c0001t0002g0304 others(5): Show |
8 | HG00544.hp1 HG00673.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-2674C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12052215 | |||||||
| chr17:12052296 | C | G | 271 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0024 others(268): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.116-2593C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12052296 | |||||||
| chr17:12052384 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.116-2505A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12052384 | |||||||
| chr17:12052494 | T | G | 2 | a0001c0002t0003g0051 a0001c0002t0003g0084 |
2 | HG00597.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.116-2395T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12052494 | |||||||
| chr17:12052610 | G | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.116-2279G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12052610 | |||||||
| chr17:12052817 | G | A | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | HG01258.hp2 HG01261.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-2072G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12052817 | |||||||
| chr17:12053359 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.116-1530G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12053359 | |||||||
| chr17:12053675 | T | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.116-1214T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12053675 | |||||||
| chr17:12053745 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.116-1144G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12053745 | |||||||
| chr17:12053807 | G | A | 1 | a0001c0001t0004g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.116-1082G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12053807 | |||||||
| chr17:12053945 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.116-944A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12053945 | |||||||
| chr17:12054299 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.116-590C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12054299 | |||||||
| chr17:12054382 | A | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(55): Show |
61 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.116-507A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12054382 | |||||||
| chr17:12054430 | C | T | 2 | a0001c0001t0001g0276 a0002c0004t0012g0027 |
2 | HG01243.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.116-459C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12054430 | |||||||
| chr17:12054736 | A | G | 265 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(262): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.116-153A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12054736 | |||||||
| chr17:12055224 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 |
3 | HG02486.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.218+233G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12055224 | |||||||
| chr17:12055299 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.218+308G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12055299 | |||||||
| chr17:12055354 | T | C | 67 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(64): Show |
67 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.218+363T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12055354 | |||||||
| chr17:12056298 | A | T | 1 | a0001c0001t0001g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.218+1307A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056298 | |||||||
| chr17:12056326 | C | CT | 61 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(58): Show |
64 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.218+1336dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12056326 | ||||||
| chr17:12056398 | A | C | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.218+1407A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056398 | |||||||
| chr17:12056434 | G | A | 1 | a0001c0001t0002g0263 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.218+1443G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056434 | |||||||
| chr17:12056502 | C | T | 122 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(119): Show |
122 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.218+1511C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056502 | |||||||
| chr17:12056666 | A | G | 1 | a0001c0001t0002g0227 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.218+1675A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056666 | |||||||
| chr17:12056774 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.218+1783T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056774 | |||||||
| chr17:12056907 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.218+1916A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056907 | |||||||
| chr17:12056918 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.218+1927C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056918 | |||||||
| chr17:12056956 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.218+1965A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056956 | |||||||
| chr17:12057159 | A | G | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.218+2168A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12057159 | |||||||
| chr17:12057332 | A | G | 61 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(58): Show |
64 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.218+2341A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12057332 | |||||||
| chr17:12057501 | G | T | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.218+2510G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12057501 | |||||||
| chr17:12057684 | C | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(17): Show |
20 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.218+2693C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12057684 | |||||||
| chr17:12057726 | G | C | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0003g0032 others(1): Show |
4 | HG00673.hp2 HG02129.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+2735G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12057726 | |||||||
| chr17:12058076 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.218+3085C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12058076 | |||||||
| chr17:12058227 | C | CT | 13 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(10): Show |
13 | HG00558.hp2 HG00642.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+3255dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12058227 | ||||||
| chr17:12058227 | CT | C | 29 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(26): Show |
29 | HG01081.hp2 HG01123.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.218+3255delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12058227 | ||||||
| chr17:12058227 | CTTTTTTT | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(11): Show |
14 | HG00733.hp2 HG00738.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+3249_218+3255d others(9): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12058227 | ||||||
| chr17:12058701 | G | A | 22 | a0001c0001t0001g0095 a0001c0001t0001g0105 a0001c0001t0001g0205 others(19): Show |
22 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.218+3710G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12058701 | |||||||
| chr17:12058833 | A | G | 1 | a0001c0001t0004g0165 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.218+3842A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12058833 | |||||||
| chr17:12058917 | C | G | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+3926C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12058917 | |||||||
| chr17:12058968 | A | T | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.218+3977A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12058968 | |||||||
| chr17:12059436 | C | T | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.218+4445C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12059436 | |||||||
| chr17:12059684 | C | T | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.218+4693C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12059684 | |||||||
| chr17:12059735 | T | G | 1 | a0001c0001t0001g0103 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.218+4744T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12059735 | |||||||
| chr17:12059866 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.218+4875T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12059866 | |||||||
| chr17:12059894 | G | A | 1 | a0001c0001t0008g0189 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218+4903G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12059894 | |||||||
| chr17:12059916 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.218+4925G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12059916 | |||||||
| chr17:12059942 | T | C | 297 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(294): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.218+4951T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12059942 | |||||||
| chr17:12060046 | T | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.218+5055T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060046 | |||||||
| chr17:12060163 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+5172C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060163 | |||||||
| chr17:12060169 | T | TA | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(3): Show |
6 | HG02055.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+5192dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12060169 | ||||||
| chr17:12060169 | TA | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.218+5192delA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12060169 | ||||||
| chr17:12060243 | T | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.218+5252T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060243 | |||||||
| chr17:12060323 | C | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02970.hp2 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.218+5332C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060323 | |||||||
| chr17:12060353 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.218+5362G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060353 | |||||||
| chr17:12060606 | A | G | 122 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(119): Show |
122 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.218+5615A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060606 | |||||||
| chr17:12060728 | G | GGGGTGT | 41 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0047 others(38): Show |
43 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.218+5738_218+5739i others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12060728 | ||||||
| chr17:12060728 | G | GGGGTGTG others(5): Show |
8 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0074 others(5): Show |
9 | HG00597.hp2 HG01934.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.218+5738_218+5739i others(14): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12060728 | ||||||
| chr17:12060730 | T | G | 1 | a0001c0001t0001g0050 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.218+5739T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060730 | |||||||
| chr17:12060748 | C | G | 1 | a0001c0001t0001g0050 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.218+5757C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060748 | |||||||
| chr17:12060748 | C | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(51): Show |
57 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.218+5757C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060748 | |||||||
| chr17:12060750 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+5759C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060750 | |||||||
| chr17:12060753 | G | C | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.218+5762G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060753 | |||||||
| chr17:12060954 | G | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+5963G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060954 | |||||||
| chr17:12061477 | T | C | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.218+6486T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12061477 | |||||||
| chr17:12061771 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+6780T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12061771 | |||||||
| chr17:12061851 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.218+6860T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12061851 | |||||||
| chr17:12061896 | G | GT | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+6914dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12061896 | ||||||
| chr17:12061906 | A | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+6915A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12061906 | |||||||
| chr17:12061927 | C | T | 3 | a0001c0001t0002g0232 a0001c0001t0002g0251 a0001c0001t0002g0252 |
3 | HG02818.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.218+6936C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12061927 | |||||||
| chr17:12062035 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.218+7044G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062035 | |||||||
| chr17:12062065 | C | A | 2 | a0001c0002t0003g0051 a0001c0002t0003g0084 |
2 | HG00597.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.218+7074C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062065 | |||||||
| chr17:12062065 | C | G | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+7074C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062065 | |||||||
| chr17:12062066 | C | G | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.218+7075C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062066 | |||||||
| chr17:12062116 | C | T | 1 | a0001c0001t0016g0234 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.218+7125C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062116 | |||||||
| chr17:12062135 | G | A | 122 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(119): Show |
122 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.218+7144G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062135 | |||||||
| chr17:12062227 | C | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00280.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.218+7236C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062227 | |||||||
| chr17:12062242 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.218+7251G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062242 | |||||||
| chr17:12062501 | A | T | 122 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(119): Show |
122 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.218+7510A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062501 | |||||||
| chr17:12062568 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.218+7577A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062568 | |||||||
| chr17:12062743 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.218+7752A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062743 | |||||||
| chr17:12062800 | G | A | 38 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0288 others(35): Show |
38 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.218+7809G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062800 | |||||||
| chr17:12063119 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.218+8128A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063119 | |||||||
| chr17:12063312 | C | G | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.218+8321C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063312 | |||||||
| chr17:12063583 | G | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+8592G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063583 | |||||||
| chr17:12063728 | T | C | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.218+8737T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063728 | |||||||
| chr17:12063739 | G | C | 1 | a0001c0001t0006g0115 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.218+8748G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063739 | |||||||
| chr17:12063749 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.218+8758G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063749 | |||||||
| chr17:12063840 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0004g0155 |
2 | HG00673.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.218+8849C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063840 | |||||||
| chr17:12063855 | C | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+8864C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063855 | |||||||
| chr17:12063904 | G | A | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG00544.hp2 HG02040.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+8913G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063904 | |||||||
| chr17:12063926 | C | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0294 |
2 | NA18949.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.218+8935C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063926 | |||||||
| chr17:12063938 | C | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0294 |
2 | NA18949.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.218+8947C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063938 | |||||||
| chr17:12063970 | CA | C | 124 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(121): Show |
124 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.218+8980delA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063970 | |||||||
| chr17:12064001 | A | T | 2 | a0001c0001t0002g0285 a0001c0001t0002g0286 |
2 | NA18986.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.218+9010A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064001 | |||||||
| chr17:12064017 | G | T | 1 | a0001c0001t0001g0246 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.218+9026G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064017 | |||||||
| chr17:12064021 | G | GGA | 53 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(50): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.218+9051_218+9052d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12064021 | ||||||
| chr17:12064023 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.218+9032A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064023 | |||||||
| chr17:12064076 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | NA18970.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.218+9085T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064076 | |||||||
| chr17:12064107 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.218+9116A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064107 | |||||||
| chr17:12064185 | A | C | 1 | a0001c0001t0001g0105 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.218+9194A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064185 | |||||||
| chr17:12064243 | C | T | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0256 others(1): Show |
4 | HG02717.hp1 NA18949.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+9252C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064243 | |||||||
| chr17:12064269 | G | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG00733.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.218+9278G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064269 | |||||||
| chr17:12064336 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.218+9345C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064336 | |||||||
| chr17:12064370 | G | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(51): Show |
57 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.218+9379G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064370 | |||||||
| chr17:12064412 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.218+9421G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064412 | |||||||
| chr17:12064812 | G | A | 2 | a0001c0001t0002g0056 a0001c0001t0002g0057 |
2 | HG01123.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.218+9821G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064812 | |||||||
| chr17:12064883 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.218+9892G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064883 | |||||||
| chr17:12065107 | G | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+10116G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065107 | |||||||
| chr17:12065196 | C | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+10205C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065196 | |||||||
| chr17:12065258 | A | ATAT | 18 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(15): Show |
18 | HG00099.hp1 HG00621.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.218+10299_218+1030 others(7): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065258 | ||||||
| chr17:12065258 | A | ATATTAT | 69 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(66): Show |
69 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.218+10296_218+1030 others(10): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065258 | ||||||
| chr17:12065258 | A | ATATTATT others(2): Show |
96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0018 others(93): Show |
96 | HG00544.hp1 HG00609.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.218+10293_218+1030 others(13): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065258 | ||||||
| chr17:12065258 | A | ATATTATT others(5): Show |
45 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(42): Show |
45 | HG01071.hp2 HG01123.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.218+10290_218+1030 others(16): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065258 | ||||||
| chr17:12065258 | A | ATATTATT others(8): Show |
5 | a0001c0001t0001g0104 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
5 | HG00558.hp2 HG02683.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+10287_218+1030 others(19): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065258 | ||||||
| chr17:12065258 | A | ATATTATT others(11): Show |
1 | a0001c0001t0004g0035 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.218+10284_218+1030 others(22): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065258 | ||||||
| chr17:12065258 | ATATTAT | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+10296_218+1030 others(10): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065258 | ||||||
| chr17:12065280 | T | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+10289T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065280 | |||||||
| chr17:12065303 | G | GT | 73 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(70): Show |
76 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.218+10325dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065303 | ||||||
| chr17:12065361 | C | T | 5 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0073 others(2): Show |
5 | HG01071.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+10370C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065361 | |||||||
| chr17:12065595 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.218+10604T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065595 | |||||||
| chr17:12065741 | A | G | 4 | a0001c0001t0002g0299 a0001c0001t0002g0300 a0001c0001t0002g0301 others(1): Show |
4 | HG00597.hp1 NA18612.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+10750A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065741 | |||||||
| chr17:12065762 | T | A | 2 | a0001c0001t0001g0276 a0002c0004t0012g0027 |
2 | HG01243.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.218+10771T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065762 | |||||||
| chr17:12065821 | G | T | 2 | a0001c0001t0002g0298 a0001c0001t0002g0312 |
2 | NA18747.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.218+10830G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065821 | |||||||
| chr17:12065924 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.218+10933G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065924 | |||||||
| chr17:12065984 | G | A | 1 | a0001c0001t0002g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.218+10993G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065984 | |||||||
| chr17:12066135 | TC | T | 52 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(49): Show |
55 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.218+11145delC | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066135 | |||||||
| chr17:12066136 | C | CT | 15 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
15 | HG01106.hp1 HG02040.hp2 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.218+11158dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12066136 | ||||||
| chr17:12066136 | CT | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(17): Show |
20 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.218+11158delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12066136 | ||||||
| chr17:12066279 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.218+11288A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066279 | |||||||
| chr17:12066356 | A | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+11365A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066356 | |||||||
| chr17:12066491 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.218+11500A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066491 | |||||||
| chr17:12066530 | T | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+11539T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066530 | |||||||
| chr17:12066669 | T | C | 1 | a0001c0001t0002g0107 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.218+11678T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066669 | |||||||
| chr17:12066687 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+11696C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066687 | |||||||
| chr17:12066712 | C | T | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+11721C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066712 | |||||||
| chr17:12066782 | C | T | 1 | a0001c0001t0004g0230 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.218+11791C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066782 | |||||||
| chr17:12066789 | A | C | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+11798A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066789 | |||||||
| chr17:12066839 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG01346.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.218+11848G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066839 | |||||||
| chr17:12066879 | C | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0002g0072 |
3 | HG00642.hp1 HG01516.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.218+11888C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066879 | |||||||
| chr17:12066967 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0050 others(3): Show |
7 | HG01934.hp2 HG02300.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+11976G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066967 | |||||||
| chr17:12066980 | A | G | 1 | a0001c0001t0004g0165 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.218+11989A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066980 | |||||||
| chr17:12067166 | G | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+12175G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067166 | |||||||
| chr17:12067234 | C | G | 70 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(67): Show |
70 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.218+12243C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067234 | |||||||
| chr17:12067336 | T | C | 1 | a0001c0001t0002g0263 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.218+12345T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067336 | |||||||
| chr17:12067361 | T | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+12370T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067361 | |||||||
| chr17:12067366 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+12375C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067366 | |||||||
| chr17:12067367 | G | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+12376G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067367 | |||||||
| chr17:12067516 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+12525C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067516 | |||||||
| chr17:12067749 | A | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+12758A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067749 | |||||||
| chr17:12067955 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.218+12964G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067955 | |||||||
| chr17:12067978 | G | A | 6 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+12987G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067978 | |||||||
| chr17:12068028 | T | G | 1 | a0001c0001t0001g0199 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.218+13037T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068028 | |||||||
| chr17:12068123 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.218+13132A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068123 | |||||||
| chr17:12068300 | C | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-13056C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068300 | |||||||
| chr17:12068366 | A | G | 13 | a0001c0001t0003g0002 a0001c0001t0003g0031 a0001c0001t0003g0054 others(10): Show |
14 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-12990A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068366 | |||||||
| chr17:12068458 | A | G | 1 | a0002c0004t0012g0027 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.219-12898A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068458 | |||||||
| chr17:12068495 | G | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-12861G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068495 | |||||||
| chr17:12068662 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.219-12694G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068662 | |||||||
| chr17:12068678 | C | T | 1 | a0002c0004t0012g0027 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.219-12678C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068678 | |||||||
| chr17:12068783 | A | ATG | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-12572_219-1257 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12068783 | ||||||
| chr17:12068785 | T | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-12571T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068785 | |||||||
| chr17:12068858 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.219-12498C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068858 | |||||||
| chr17:12069102 | A | G | 118 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(115): Show |
118 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.219-12254A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069102 | |||||||
| chr17:12069432 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.219-11924T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069432 | |||||||
| chr17:12069449 | C | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0057 |
2 | HG01123.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.219-11907C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069449 | |||||||
| chr17:12069573 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.219-11783A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069573 | |||||||
| chr17:12069711 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.219-11645C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069711 | |||||||
| chr17:12069729 | G | A | 6 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0299 others(3): Show |
6 | HG00597.hp1 NA18612.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-11627G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069729 | |||||||
| chr17:12069749 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.219-11607C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069749 | |||||||
| chr17:12069750 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-11606G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069750 | |||||||
| chr17:12069890 | C | CAT | 7 | a0001c0001t0001g0092 a0001c0001t0001g0242 a0001c0001t0002g0298 others(4): Show |
7 | HG01361.hp2 HG01891.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-11405_219-1140 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | C | CATAT | 5 | a0001c0001t0001g0137 a0001c0001t0001g0144 a0001c0001t0002g0285 others(2): Show |
5 | HG00673.hp2 HG01261.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-11407_219-1140 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CAT | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0023 others(8): Show |
11 | HG01071.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-11405_219-1140 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATAT | C | 20 | a0001c0001t0001g0020 a0001c0001t0001g0148 a0001c0001t0001g0161 others(17): Show |
20 | HG01123.hp2 HG02109.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.219-11407_219-1140 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATAT | C | 23 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0018 others(20): Show |
23 | HG00099.hp1 HG00639.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.219-11409_219-1140 others(10): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATATA others(1): Show |
C | 21 | a0001c0001t0001g0030 a0001c0001t0001g0062 a0001c0001t0001g0145 others(18): Show |
21 | HG01361.hp1 HG01934.hp1 HG01975.hp1 others(18): Show |
intron_variant | MODIFIER | c.219-11411_219-1140 others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATATA others(3): Show |
C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0073 a0001c0001t0001g0089 others(22): Show |
25 | HG00544.hp2 HG00733.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.219-11413_219-1140 others(14): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATATA others(5): Show |
C | 17 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(14): Show |
17 | HG00099.hp2 HG00544.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.219-11415_219-1140 others(16): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATATA others(7): Show |
C | 24 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0088 others(21): Show |
24 | HG00280.hp1 HG00621.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.219-11417_219-1140 others(18): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATATA others(9): Show |
C | 19 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0055 others(16): Show |
20 | HG00609.hp1 HG01256.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.219-11419_219-1140 others(20): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATATA others(11): Show |
C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0049 others(41): Show |
46 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.219-11421_219-1140 others(22): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATATA others(13): Show |
C | 19 | a0001c0001t0001g0028 a0001c0001t0001g0053 a0001c0001t0001g0060 others(16): Show |
19 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-11423_219-1140 others(24): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATATA others(15): Show |
C | 10 | a0001c0001t0001g0080 a0001c0001t0001g0105 a0001c0001t0001g0138 others(7): Show |
10 | HG01255.hp1 HG01255.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-11425_219-1140 others(26): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATATA others(17): Show |
C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0104 others(9): Show |
12 | HG02109.hp1 HG02258.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-11427_219-1140 others(28): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATATA others(19): Show |
C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(11): Show |
14 | HG00280.hp2 HG01081.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.219-11429_219-1140 others(30): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATATA others(21): Show |
C | 18 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(15): Show |
18 | HG00558.hp1 HG01106.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.219-11431_219-1140 others(32): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATATA others(23): Show |
C | 5 | a0001c0001t0001g0243 a0001c0001t0004g0041 a0001c0001t0004g0042 others(2): Show |
5 | HG01243.hp2 HG02572.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-11433_219-1140 others(34): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATATA others(25): Show |
C | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
3 | HG02647.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.219-11435_219-1140 others(36): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATATA others(37): Show |
C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0130 |
2 | HG03453.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.219-11447_219-1140 others(48): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069890 | CATATATA others(39): Show |
C | 1 | a0001c0001t0001g0194 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.219-11449_219-1140 others(50): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | ||||||
| chr17:12069900 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.219-11456T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069900 | |||||||
| chr17:12069907 | A | C | 1 | a0001c0001t0002g0304 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.219-11449A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069907 | |||||||
| chr17:12069919 | ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0256 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.219-11436_219-1142 others(19): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069919 | |||||||
| chr17:12069925 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.219-11430_219-1142 others(15): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069925 | |||||||
| chr17:12069930 | T | C | 17 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0001t0002g0260 others(14): Show |
17 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.219-11426T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069930 | |||||||
| chr17:12069935 | A | C | 1 | a0001c0001t0001g0256 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.219-11421A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069935 | |||||||
| chr17:12069935 | ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0140 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.219-11420_219-1140 others(19): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069935 | |||||||
| chr17:12069976 | A | AGC | 71 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(68): Show |
71 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.219-11379_219-1137 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069976 | ||||||
| chr17:12070174 | T | TA | 6 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-11181dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12070174 | ||||||
| chr17:12070263 | CAT | C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0138 a0001c0001t0001g0235 |
3 | HG00280.hp1 HG00639.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.219-11092_219-1109 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070263 | |||||||
| chr17:12070266 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.219-11090G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070266 | |||||||
| chr17:12070348 | A | G | 1 | a0001c0001t0003g0070 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.219-11008A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070348 | |||||||
| chr17:12070559 | G | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-10797G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070559 | |||||||
| chr17:12070592 | T | C | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.219-10764T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070592 | |||||||
| chr17:12070683 | T | C | 265 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(262): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.219-10673T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070683 | |||||||
| chr17:12070753 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0239 |
2 | HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.219-10603A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070753 | |||||||
| chr17:12070963 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.219-10393T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070963 | |||||||
| chr17:12070991 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-10365C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070991 | |||||||
| chr17:12070992 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-10364C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070992 | |||||||
| chr17:12070993 | C | G | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-10363C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070993 | |||||||
| chr17:12071166 | C | A | 1 | a0001c0001t0002g0107 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.219-10190C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12071166 | |||||||
| chr17:12071166 | C | G | 1 | a0001c0001t0002g0106 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.219-10190C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12071166 | |||||||
| chr17:12071228 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-10128C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12071228 | |||||||
| chr17:12071257 | A | G | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG01934.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.219-10099A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12071257 | |||||||
| chr17:12072816 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-8540C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12072816 | |||||||
| chr17:12072828 | A | G | 2 | a0001c0001t0001g0276 a0001c0001t0013g0005 |
2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.219-8528A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12072828 | |||||||
| chr17:12072976 | A | G | 1 | a0001c0001t0003g0068 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.219-8380A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12072976 | |||||||
| chr17:12073183 | T | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-8173T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073183 | |||||||
| chr17:12073191 | A | T | 1 | a0001c0001t0001g0048 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.219-8165A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073191 | |||||||
| chr17:12073202 | C | G | 2 | a0001c0001t0002g0259 a0001c0001t0002g0265 |
2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.219-8154C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073202 | |||||||
| chr17:12073219 | T | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(5): Show |
8 | HG02055.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.219-8137T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073219 | |||||||
| chr17:12073245 | A | G | 4 | a0001c0001t0001g0190 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
4 | NA18966.hp1 NA18979.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-8111A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073245 | |||||||
| chr17:12073635 | T | C | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
4 | HG02451.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-7721T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073635 | |||||||
| chr17:12073667 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.219-7689G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073667 | |||||||
| chr17:12073770 | A | AT | 102 | a0001c0001t0001g0011 a0001c0001t0001g0110 a0001c0001t0001g0120 others(99): Show |
102 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.219-7568dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12073770 | ||||||
| chr17:12073770 | ATT | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(51): Show |
57 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.219-7569_219-7568d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12073770 | ||||||
| chr17:12073812 | G | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(48): Show |
54 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.219-7544G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073812 | |||||||
| chr17:12073867 | G | A | 1 | a0001c0001t0005g0186 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.219-7489G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073867 | |||||||
| chr17:12073963 | G | A | 72 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(69): Show |
72 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.219-7393G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073963 | |||||||
| chr17:12074075 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(256): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.219-7281T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074075 | |||||||
| chr17:12074238 | A | G | 3 | a0001c0001t0006g0111 a0001c0001t0006g0115 a0001c0001t0006g0126 |
3 | NA18967.hp2 NA19060.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.219-7118A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074238 | |||||||
| chr17:12074264 | T | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG01346.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.219-7092T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074264 | |||||||
| chr17:12074335 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.219-7021G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074335 | |||||||
| chr17:12074509 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.219-6847A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074509 | |||||||
| chr17:12074635 | G | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(184): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.219-6721G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074635 | |||||||
| chr17:12074658 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.219-6698A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074658 | |||||||
| chr17:12074667 | G | C | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-6689G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074667 | |||||||
| chr17:12074759 | G | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-6597G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074759 | |||||||
| chr17:12074770 | G | T | 118 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(115): Show |
118 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.219-6586G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074770 | |||||||
| chr17:12075062 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0172 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.219-6294T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12075062 | |||||||
| chr17:12075077 | T | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-6279T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12075077 | |||||||
| chr17:12075083 | C | T | 1 | a0001c0001t0002g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.219-6273C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12075083 | |||||||
| chr17:12075387 | T | A | 3 | a0001c0001t0002g0261 a0001c0001t0002g0266 a0001c0001t0002g0271 |
3 | HG00639.hp2 HG02602.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.219-5969T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12075387 | |||||||
| chr17:12075401 | A | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-5955A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12075401 | |||||||
| chr17:12075431 | A | G | 1 | a0001c0001t0007g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.219-5925A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12075431 | |||||||
| chr17:12075551 | G | A | 6 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0299 others(3): Show |
6 | HG00597.hp1 NA18612.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-5805G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12075551 | |||||||
| chr17:12076106 | A | G | 24 | a0001c0001t0001g0045 a0001c0001t0001g0104 a0001c0001t0001g0184 others(21): Show |
24 | HG00099.hp1 HG02015.hp2 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.219-5250A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076106 | |||||||
| chr17:12076113 | T | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0131 |
3 | HG00621.hp2 NA18969.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.219-5243T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076113 | |||||||
| chr17:12076279 | C | CTG | 42 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0102 others(39): Show |
42 | HG00280.hp1 HG00544.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.219-5031_219-5030d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | ||||||
| chr17:12076279 | C | CTGTG | 88 | a0001c0001t0001g0045 a0001c0001t0001g0104 a0001c0001t0001g0105 others(85): Show |
88 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.219-5033_219-5030d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | ||||||
| chr17:12076279 | C | CTGTGTG | 27 | a0001c0001t0001g0012 a0001c0001t0001g0095 a0001c0001t0001g0114 others(24): Show |
27 | HG00597.hp1 HG00642.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.219-5035_219-5030d others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | ||||||
| chr17:12076279 | C | CTGTGTGT others(1): Show |
5 | a0001c0001t0001g0101 a0001c0001t0001g0130 a0001c0001t0001g0294 others(2): Show |
5 | HG04115.hp2 NA18747.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-5037_219-5030d others(10): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | ||||||
| chr17:12076279 | C | CTGTGTGT others(3): Show |
2 | a0001c0001t0001g0103 a0001c0001t0001g0184 |
2 | HG00099.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.219-5039_219-5030d others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | ||||||
| chr17:12076279 | C | CTGTGTGT others(7): Show |
2 | a0001c0001t0001g0139 a0001c0001t0001g0144 |
2 | HG01261.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.219-5043_219-5030d others(16): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | ||||||
| chr17:12076279 | C | CTGTGTGT others(9): Show |
1 | a0001c0001t0001g0145 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.219-5045_219-5030d others(18): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | ||||||
| chr17:12076279 | CTG | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(63): Show |
68 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.219-5031_219-5030d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | ||||||
| chr17:12076279 | CTGTG | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0028 others(6): Show |
9 | HG00558.hp1 HG02258.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-5033_219-5030d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | ||||||
| chr17:12076279 | CTGTGTG | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0049 others(4): Show |
7 | HG00738.hp2 HG01243.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-5035_219-5030d others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | ||||||
| chr17:12076279 | CTGTGTGT others(1): Show |
C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0243 others(4): Show |
7 | HG02055.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-5037_219-5030d others(10): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | ||||||
| chr17:12076279 | CTGTGTGT others(3): Show |
C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0022 |
2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.219-5039_219-5030d others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | ||||||
| chr17:12076279 | CTGTGTGT others(13): Show |
C | 1 | a0001c0001t0001g0129 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.219-5049_219-5030d others(22): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | ||||||
| chr17:12076283 | G | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0100 a0001c0001t0001g0176 others(1): Show |
4 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-5073G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076283 | |||||||
| chr17:12076388 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-4968A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076388 | |||||||
| chr17:12076532 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.219-4824T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076532 | |||||||
| chr17:12076721 | T | TC | 118 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(115): Show |
118 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.219-4634dupC | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076721 | ||||||
| chr17:12076857 | T | TTG | 90 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(87): Show |
90 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.219-4483_219-4482d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076857 | ||||||
| chr17:12076857 | T | TTGTG | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.219-4485_219-4482d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076857 | ||||||
| chr17:12076882 | G | C | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00280.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.219-4474G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076882 | |||||||
| chr17:12076911 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.219-4445T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076911 | |||||||
| chr17:12076954 | G | A | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-4402G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076954 | |||||||
| chr17:12077026 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0100 |
2 | HG01192.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.219-4330G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12077026 | |||||||
| chr17:12077154 | T | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0123 a0001c0001t0001g0236 |
3 | HG02165.hp2 NA18946.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.219-4202T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12077154 | |||||||
| chr17:12077206 | G | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.219-4150G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12077206 | |||||||
| chr17:12077486 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219-3870A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12077486 | |||||||
| chr17:12077630 | C | G | 1 | a0001c0001t0001g0200 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.219-3726C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12077630 | |||||||
| chr17:12077761 | C | T | 132 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(129): Show |
132 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.219-3595C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12077761 | |||||||
| chr17:12078024 | C | T | 1 | a0001c0001t0002g0298 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.219-3332C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078024 | |||||||
| chr17:12078046 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.219-3310G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078046 | |||||||
| chr17:12078128 | A | C | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-3228A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078128 | |||||||
| chr17:12078129 | G | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-3227G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078129 | |||||||
| chr17:12078235 | G | T | 3 | a0001c0001t0002g0232 a0001c0001t0002g0251 a0001c0001t0002g0252 |
3 | HG02818.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.219-3121G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078235 | |||||||
| chr17:12078644 | G | C | 265 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(262): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.219-2712G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078644 | |||||||
| chr17:12078693 | A | G | 1 | a0001c0001t0003g0070 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.219-2663A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078693 | |||||||
| chr17:12078811 | C | T | 1 | a0001c0001t0006g0094 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.219-2545C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078811 | |||||||
| chr17:12079093 | A | G | 1 | a0001c0001t0004g0029 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.219-2263A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12079093 | |||||||
| chr17:12079132 | G | T | 1 | a0001c0001t0001g0276 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.219-2224G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12079132 | |||||||
| chr17:12079134 | TTTTAGTA others(2): Show |
T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-2208_219-2200d others(11): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12079134 | ||||||
| chr17:12079238 | T | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-2118T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12079238 | |||||||
| chr17:12079524 | C | T | 1 | a0001c0001t0003g0068 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.219-1832C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12079524 | |||||||
| chr17:12079985 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.219-1371G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12079985 | |||||||
| chr17:12080237 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.219-1119A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080237 | |||||||
| chr17:12080270 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.219-1086C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080270 | |||||||
| chr17:12080434 | T | G | 1 | a0001c0001t0001g0108 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.219-922T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080434 | |||||||
| chr17:12080487 | A | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-869A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080487 | |||||||
| chr17:12080571 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.219-785C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080571 | |||||||
| chr17:12080734 | C | T | 8 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(5): Show |
8 | NA18964.hp2 NA18977.hp2 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.219-622C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080734 | |||||||
| chr17:12080897 | A | G | 5 | a0001c0001t0001g0272 a0001c0001t0002g0287 a0001c0001t0002g0291 others(2): Show |
5 | HG02132.hp1 HG03654.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-459A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080897 | |||||||
| chr17:12080915 | G | C | 118 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(115): Show |
118 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.219-441G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080915 | |||||||
| chr17:12081022 | C | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.219-334C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12081022 | |||||||
| chr17:12081039 | A | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0002g0072 |
3 | HG00642.hp1 HG01516.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.219-317A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12081039 | |||||||
| chr17:12081057 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.219-299A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12081057 | |||||||
| chr17:12081710 | A | T | 1 | a0001c0001t0002g0056 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.393+180A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12081710 | |||||||
| chr17:12081832 | A | C | 1 | a0001c0001t0007g0248 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.393+302A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12081832 | |||||||
| chr17:12082187 | T | C | 70 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(67): Show |
70 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.393+657T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12082187 | |||||||
| chr17:12082226 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0021 others(1): Show |
4 | HG02809.hp2 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+696G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12082226 | |||||||
| chr17:12082257 | T | C | 118 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(115): Show |
118 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.393+727T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12082257 | |||||||
| chr17:12082630 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.393+1100C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12082630 | |||||||
| chr17:12082635 | C | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.393+1105C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12082635 | |||||||
| chr17:12082784 | G | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.393+1254G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12082784 | |||||||
| chr17:12082952 | C | G | 3 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02970.hp2 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.393+1422C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12082952 | |||||||
| chr17:12083160 | A | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.393+1630A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12083160 | |||||||
| chr17:12083517 | G | A | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.393+1987G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12083517 | |||||||
| chr17:12083672 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.393+2142A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12083672 | |||||||
| chr17:12084125 | C | T | 1 | a0001c0001t0002g0260 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.393+2595C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12084125 | |||||||
| chr17:12084337 | C | T | 1 | a0001c0001t0002g0310 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.393+2807C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12084337 | |||||||
| chr17:12084428 | C | T | 1 | a0001c0001t0019g0295 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.393+2898C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12084428 | |||||||
| chr17:12084501 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.393+2971A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12084501 | |||||||
| chr17:12084548 | A | G | 5 | a0001c0001t0004g0026 a0001c0001t0004g0029 a0001c0001t0004g0038 others(2): Show |
5 | HG02040.hp2 NA18945.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+3018A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12084548 | |||||||
| chr17:12084594 | C | T | 70 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(67): Show |
70 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.393+3064C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12084594 | |||||||
| chr17:12084733 | G | A | 2 | a0001c0003t0001g0279 a0001c0003t0002g0280 |
2 | HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.393+3203G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12084733 | |||||||
| chr17:12084928 | G | GAGAA | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.393+3401_393+3402i others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12084928 | ||||||
| chr17:12085494 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.393+3964C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12085494 | |||||||
| chr17:12085599 | G | T | 70 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(67): Show |
70 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.393+4069G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12085599 | |||||||
| chr17:12085773 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0063 |
2 | HG01081.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.393+4243A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12085773 | |||||||
| chr17:12085850 | T | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.393+4320T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12085850 | |||||||
| chr17:12086244 | G | A | 23 | a0001c0001t0001g0095 a0001c0001t0001g0105 a0001c0001t0001g0182 others(20): Show |
23 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.393+4714G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12086244 | |||||||
| chr17:12086446 | A | G | 4 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG01123.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+4916A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12086446 | |||||||
| chr17:12086599 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG02109.hp2 HG02145.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+5069C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12086599 | |||||||
| chr17:12086826 | T | TTTTTG | 41 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(38): Show |
41 | HG01106.hp1 HG01243.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.393+5331_393+5335d others(7): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12086826 | ||||||
| chr17:12086826 | T | TTTTTGTT others(3): Show |
5 | a0001c0001t0001g0036 a0001c0001t0002g0232 a0001c0001t0002g0251 others(2): Show |
5 | HG02818.hp2 HG02976.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+5326_393+5335d others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12086826 | ||||||
| chr17:12086826 | TTTTTG | T | 116 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(113): Show |
116 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.393+5331_393+5335d others(7): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12086826 | ||||||
| chr17:12086826 | TTTTTGTT others(3): Show |
T | 124 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0030 others(121): Show |
127 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.393+5326_393+5335d others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12086826 | ||||||
| chr17:12086826 | TTTTTGTT others(8): Show |
T | 1 | a0001c0001t0001g0024 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.393+5321_393+5335d others(17): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12086826 | ||||||
| chr17:12087007 | C | T | 1 | a0001c0001t0002g0298 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.393+5477C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087007 | |||||||
| chr17:12087090 | G | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+5560G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087090 | |||||||
| chr17:12087092 | C | T | 1 | a0001c0001t0002g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.393+5562C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087092 | |||||||
| chr17:12087140 | G | A | 2 | a0001c0001t0002g0298 a0001c0001t0002g0312 |
2 | NA18747.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.393+5610G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087140 | |||||||
| chr17:12087307 | G | A | 3 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02970.hp2 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.393+5777G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087307 | |||||||
| chr17:12087362 | A | G | 118 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(115): Show |
118 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.393+5832A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087362 | |||||||
| chr17:12087502 | T | C | 1 | a0001c0001t0002g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.393+5972T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087502 | |||||||
| chr17:12087546 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.393+6016C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087546 | |||||||
| chr17:12087616 | T | TATTA | 8 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(5): Show |
8 | HG02451.hp2 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+6105_393+6108d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12087616 | ||||||
| chr17:12087616 | TATTA | T | 17 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0001t0002g0260 others(14): Show |
17 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.393+6105_393+6108d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12087616 | ||||||
| chr17:12087813 | T | G | 1 | a0001c0001t0002g0315 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.393+6283T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087813 | |||||||
| chr17:12087847 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.393+6317C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087847 | |||||||
| chr17:12087854 | T | C | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.393+6324T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087854 | |||||||
| chr17:12088151 | G | C | 6 | a0001c0001t0001g0273 a0001c0001t0001g0277 a0001c0001t0001g0281 others(3): Show |
6 | HG02055.hp2 HG02451.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+6621G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088151 | |||||||
| chr17:12088445 | T | TATATATT others(9): Show |
290 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(287): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.393+6930_393+6931i others(18): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088445 | ||||||
| chr17:12088458 | T | TTAAATAT others(6): Show |
2 | a0001c0001t0001g0206 a0001c0001t0018g0046 |
2 | HG02040.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.393+6930_393+6931i others(15): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088458 | ||||||
| chr17:12088461 | T | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.393+6931T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088461 | |||||||
| chr17:12088496 | T | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(54): Show |
60 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.393+6966T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088496 | |||||||
| chr17:12088507 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.393+6977C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088507 | |||||||
| chr17:12088541 | A | G | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.393+7011A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088541 | |||||||
| chr17:12088541 | AT | A | 116 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(113): Show |
116 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.393+7013delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088541 | ||||||
| chr17:12088548 | C | A | 118 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(115): Show |
118 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.393+7018C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088548 | |||||||
| chr17:12088548 | C | G | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.393+7018C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088548 | |||||||
| chr17:12088568 | A | AAT | 195 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0095 others(192): Show |
195 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.394-7001_394-7000d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088568 | ||||||
| chr17:12088568 | A | AATATATA others(22): Show |
54 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(51): Show |
57 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.394-7000_394-6999i others(31): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088568 | ||||||
| chr17:12088575 | A | T | 1 | a0001c0001t0001g0278 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.394-7000A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088575 | |||||||
| chr17:12088576 | A | T | 15 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
15 | HG01106.hp1 HG02040.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.394-6999A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088576 | |||||||
| chr17:12088577 | T | A | 15 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
15 | HG01106.hp1 HG02040.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.394-6998T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088577 | |||||||
| chr17:12088583 | A | T | 15 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
15 | HG01106.hp1 HG02040.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.394-6992A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088583 | |||||||
| chr17:12088584 | T | A | 15 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
15 | HG01106.hp1 HG02040.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.394-6991T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088584 | |||||||
| chr17:12088592 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.394-6983A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088592 | |||||||
| chr17:12088618 | G | GATTA | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-6955_394-6952d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088618 | ||||||
| chr17:12088646 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.394-6929T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088646 | |||||||
| chr17:12088778 | A | C | 5 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0242 others(2): Show |
5 | HG02083.hp1 NA18982.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-6797A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088778 | |||||||
| chr17:12088911 | C | CT | 8 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0195 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-6646dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088911 | ||||||
| chr17:12088911 | CT | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(60): Show |
66 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.394-6646delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088911 | ||||||
| chr17:12088942 | C | T | 1 | a0001c0001t0003g0071 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.394-6633C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088942 | |||||||
| chr17:12088991 | A | G | 9 | a0001c0001t0001g0190 a0001c0001t0001g0195 a0001c0001t0001g0198 others(6): Show |
9 | HG02165.hp1 NA18944.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-6584A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088991 | |||||||
| chr17:12089004 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.394-6571C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089004 | |||||||
| chr17:12089060 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394-6515C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089060 | |||||||
| chr17:12089110 | C | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.394-6465C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089110 | |||||||
| chr17:12089164 | G | A | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.394-6411G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089164 | |||||||
| chr17:12089213 | A | G | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(289): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.394-6362A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089213 | |||||||
| chr17:12089614 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.394-5961A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089614 | |||||||
| chr17:12089976 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.394-5599G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089976 | |||||||
| chr17:12089981 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.394-5594C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089981 | |||||||
| chr17:12090051 | A | G | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-5524A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090051 | |||||||
| chr17:12090056 | C | G | 1 | a0001c0001t0002g0319 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.394-5519C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090056 | |||||||
| chr17:12090214 | A | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(1): Show |
4 | HG02486.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-5361A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090214 | |||||||
| chr17:12090472 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.394-5103A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090472 | |||||||
| chr17:12090482 | G | T | 1 | a0001c0001t0001g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.394-5093G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090482 | |||||||
| chr17:12090555 | G | T | 1 | a0001c0001t0001g0153 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.394-5020G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090555 | |||||||
| chr17:12090750 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0166 |
2 | HG02258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.394-4825T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090750 | |||||||
| chr17:12090862 | G | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-4713G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090862 | |||||||
| chr17:12090887 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.394-4688C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090887 | |||||||
| chr17:12091078 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.394-4497G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12091078 | |||||||
| chr17:12091183 | A | G | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-4392A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12091183 | |||||||
| chr17:12091238 | G | A | 1 | a0001c0001t0003g0079 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.394-4337G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12091238 | |||||||
| chr17:12091455 | A | T | 71 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(68): Show |
71 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.394-4120A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12091455 | |||||||
| chr17:12091553 | C | G | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-4022C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12091553 | |||||||
| chr17:12091742 | T | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-3833T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12091742 | |||||||
| chr17:12091799 | A | G | 71 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(68): Show |
71 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.394-3776A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12091799 | |||||||
| chr17:12092034 | G | C | 71 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(68): Show |
71 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.394-3541G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092034 | |||||||
| chr17:12092078 | A | G | 1 | a0001c0001t0004g0290 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.394-3497A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092078 | |||||||
| chr17:12092285 | G | A | 1 | a0001c0001t0002g0291 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.394-3290G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092285 | |||||||
| chr17:12092684 | C | G | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-2891C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092684 | |||||||
| chr17:12092706 | A | G | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-2869A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092706 | |||||||
| chr17:12092748 | C | A | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.394-2827C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092748 | |||||||
| chr17:12092749 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394-2826G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092749 | |||||||
| chr17:12092793 | G | A | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-2782G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092793 | |||||||
| chr17:12092801 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.394-2774C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092801 | |||||||
| chr17:12092851 | C | G | 1 | a0001c0001t0003g0061 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.394-2724C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092851 | |||||||
| chr17:12092862 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.394-2713T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092862 | |||||||
| chr17:12092918 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0100 a0001c0001t0001g0176 others(1): Show |
4 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-2657C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092918 | |||||||
| chr17:12092941 | G | A | 1 | a0001c0001t0019g0295 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.394-2634G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092941 | |||||||
| chr17:12092981 | G | A | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.394-2594G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092981 | |||||||
| chr17:12092984 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.394-2591C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092984 | |||||||
| chr17:12093046 | T | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-2529T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12093046 | |||||||
| chr17:12093144 | T | C | 1 | a0001c0001t0002g0316 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.394-2431T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12093144 | |||||||
| chr17:12093211 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.394-2364A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12093211 | |||||||
| chr17:12093317 | A | G | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(289): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.394-2258A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12093317 | |||||||
| chr17:12093379 | A | T | 3 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 |
3 | HG01099.hp2 HG01123.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.394-2196A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12093379 | |||||||
| chr17:12093511 | T | A | 1 | a0001c0001t0001g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.394-2064T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12093511 | |||||||
| chr17:12093987 | T | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.394-1588T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12093987 | |||||||
| chr17:12094172 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.394-1403G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12094172 | |||||||
| chr17:12094311 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.394-1264C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12094311 | |||||||
| chr17:12094327 | C | G | 1 | a0001c0001t0001g0214 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.394-1248C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12094327 | |||||||
| chr17:12094375 | C | T | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(289): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.394-1200C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12094375 | |||||||
| chr17:12094628 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.394-947A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12094628 | |||||||
| chr17:12094725 | GGGA | G | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-844_394-842del others(3): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12094725 | ||||||
| chr17:12095166 | A | C | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.394-409A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12095166 | |||||||
| chr17:12095204 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.394-371T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12095204 | |||||||
| chr17:12095231 | G | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-344G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12095231 | |||||||
| chr17:12095830 | G | A | 265 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(262): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.513+136G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12095830 | |||||||
| chr17:12095895 | T | TGTGTGTG others(10): Show |
1 | a0001c0001t0007g0248 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.513+201_513+202ins others(17): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12095895 | |||||||
| chr17:12095895 | T | TTG | 26 | a0001c0001t0001g0033 a0001c0001t0001g0052 a0001c0001t0001g0055 others(23): Show |
26 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.513+233_513+234dup others(2): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | T | TTGTG | 42 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0053 others(39): Show |
44 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.513+231_513+234dup others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | T | TTGTGTG | 6 | a0001c0001t0001g0081 a0001c0001t0001g0096 a0001c0001t0001g0159 others(3): Show |
6 | HG00642.hp1 HG01884.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+229_513+234dup others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | T | TTGTGTGT others(1): Show |
6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0021 others(3): Show |
6 | HG02109.hp1 HG02809.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+227_513+234dup others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.513+225_513+234dup others(10): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | T | TTGTGTGT others(5): Show |
2 | a0001c0001t0007g0249 a0001c0001t0011g0017 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.513+223_513+234dup others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0007g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.513+221_513+234dup others(14): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | T | TTGTGTGT others(9): Show |
2 | a0001c0001t0001g0018 a0001c0001t0001g0023 |
2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.513+219_513+234dup others(16): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | T | TTGTGTGT others(11): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0019 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.513+217_513+234dup others(18): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | TTG | T | 28 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0161 others(25): Show |
28 | HG01243.hp2 HG01361.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.513+233_513+234del others(2): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | TTGTG | T | 59 | a0001c0001t0001g0010 a0001c0001t0001g0101 a0001c0001t0001g0102 others(56): Show |
59 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.513+231_513+234del others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | TTGTGTG | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
6 | HG01975.hp1 HG02273.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.513+229_513+234del others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | TTGTGTGT others(1): Show |
T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0048 others(6): Show |
10 | HG00558.hp1 HG01934.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.513+227_513+234del others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | TTGTGTGT others(3): Show |
T | 10 | a0001c0001t0001g0099 a0001c0001t0001g0157 a0001c0001t0001g0250 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.513+225_513+234del others(10): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.513+223_513+234del others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0001g0108 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.513+221_513+234del others(14): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | TTGTGTGT others(9): Show |
T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0222 |
2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.513+219_513+234del others(16): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095895 | TTGTGTGT others(11): Show |
T | 1 | a0001c0001t0001g0154 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.513+217_513+234del others(18): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | ||||||
| chr17:12095927 | G | A | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.513+233G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12095927 | |||||||
| chr17:12095929 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.513+235A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12095929 | |||||||
| chr17:12096063 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.513+369C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096063 | |||||||
| chr17:12096067 | T | TC | 30 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0099 others(27): Show |
30 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.513+394dupC | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | ||||||
| chr17:12096067 | T | TCC | 23 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(20): Show |
23 | HG00639.hp2 HG01081.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.513+393_513+394dup others(2): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | ||||||
| chr17:12096067 | T | TCCCCCCC others(6): Show |
1 | a0001c0001t0001g0128 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.513+382_513+394dup others(13): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | ||||||
| chr17:12096067 | TC | T | 38 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(35): Show |
38 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.513+394delC | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | ||||||
| chr17:12096067 | TCC | T | 42 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0102 others(39): Show |
42 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.513+393_513+394del others(2): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | ||||||
| chr17:12096067 | TCCC | T | 21 | a0001c0001t0001g0116 a0001c0001t0001g0157 a0001c0001t0001g0162 others(18): Show |
21 | HG00280.hp2 HG01891.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.513+392_513+394del others(3): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | ||||||
| chr17:12096067 | TCCCC | T | 14 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0114 others(11): Show |
14 | HG02015.hp2 HG02071.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.513+391_513+394del others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | ||||||
| chr17:12096067 | TCCCCCCC others(1): Show |
T | 26 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0030 others(23): Show |
26 | HG00597.hp2 HG00609.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.513+387_513+394del others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | ||||||
| chr17:12096067 | TCCCCCCC others(2): Show |
T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 others(22): Show |
27 | HG00099.hp2 HG00558.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.513+386_513+394del others(9): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | ||||||
| chr17:12096067 | TCCCCCCC others(4): Show |
T | 1 | a0001c0001t0004g0039 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.513+384_513+394del others(11): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | ||||||
| chr17:12096067 | TCCCCCCC others(5): Show |
T | 13 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(10): Show |
13 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.513+383_513+394del others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | ||||||
| chr17:12096067 | TCCCCCCC others(6): Show |
T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0106 |
3 | HG06807.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.513+382_513+394del others(13): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | ||||||
| chr17:12096067 | TCCCCCCC others(7): Show |
T | 6 | a0001c0001t0001g0276 a0001c0001t0002g0232 a0001c0001t0002g0251 others(3): Show |
6 | HG01243.hp2 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.513+381_513+394del others(14): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | ||||||
| chr17:12096089 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.513+395G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096089 | |||||||
| chr17:12096176 | A | T | 1 | a0001c0001t0001g0024 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.513+482A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096176 | |||||||
| chr17:12096380 | A | G | 1 | a0001c0001t0017g0077 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.513+686A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096380 | |||||||
| chr17:12096477 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.513+783C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096477 | |||||||
| chr17:12096562 | T | G | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.513+868T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096562 | |||||||
| chr17:12096784 | A | C | 1 | a0001c0001t0001g0109 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.513+1090A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096784 | |||||||
| chr17:12096925 | A | G | 1 | a0001c0001t0004g0223 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.513+1231A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096925 | |||||||
| chr17:12096956 | T | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0022 |
3 | HG02055.hp1 HG02647.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.513+1262T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096956 | |||||||
| chr17:12097016 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.513+1322G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12097016 | |||||||
| chr17:12097267 | A | G | 134 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(131): Show |
134 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.513+1573A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12097267 | |||||||
| chr17:12097315 | G | A | 194 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(191): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.513+1621G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12097315 | |||||||
| chr17:12097504 | A | G | 3 | a0001c0001t0004g0035 a0001c0001t0004g0039 a0001c0001t0004g0040 |
3 | NA18971.hp1 NA18972.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.513+1810A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12097504 | |||||||
| chr17:12097730 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0147 |
2 | NA18945.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.513+2036A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12097730 | |||||||
| chr17:12097760 | A | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.513+2066A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12097760 | |||||||
| chr17:12097879 | T | A | 1 | a0001c0001t0001g0240 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.513+2185T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12097879 | |||||||
| chr17:12098114 | A | T | 1 | a0001c0001t0009g0001 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.513+2420A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12098114 | |||||||
| chr17:12098254 | C | T | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.513+2560C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12098254 | |||||||
| chr17:12098362 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0166 |
2 | HG02258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.513+2668C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12098362 | |||||||
| chr17:12098400 | T | C | 265 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(262): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.513+2706T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12098400 | |||||||
| chr17:12098437 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.513+2743C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12098437 | |||||||
| chr17:12098477 | C | CA | 51 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0030 others(48): Show |
53 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.513+2798dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12098477 | ||||||
| chr17:12098709 | A | T | 4 | a0001c0001t0005g0186 a0001c0001t0005g0196 a0001c0001t0005g0197 others(1): Show |
4 | HG02083.hp2 NA18950.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+3015A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12098709 | |||||||
| chr17:12098913 | T | A | 1 | a0001c0001t0001g0240 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.513+3219T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12098913 | |||||||
| chr17:12099102 | T | C | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(3): Show |
6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+3408T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099102 | |||||||
| chr17:12099213 | C | CA | 12 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0020 others(9): Show |
12 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.513+3532dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12099213 | ||||||
| chr17:12099228 | A | C | 1 | a0001c0001t0001g0180 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.513+3534A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099228 | |||||||
| chr17:12099318 | A | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(52): Show |
58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.513+3624A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099318 | |||||||
| chr17:12099408 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0004g0155 |
2 | HG00673.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.513+3714G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099408 | |||||||
| chr17:12099618 | A | G | 3 | a0001c0001t0002g0261 a0001c0001t0002g0266 a0001c0001t0002g0271 |
3 | HG00639.hp2 HG02602.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.513+3924A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099618 | |||||||
| chr17:12099689 | C | G | 1 | a0001c0001t0001g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.513+3995C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099689 | |||||||
| chr17:12099720 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.513+4026A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099720 | |||||||
| chr17:12099724 | A | G | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.513+4030A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099724 | |||||||
| chr17:12099985 | C | G | 1 | a0001c0001t0005g0197 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.513+4291C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099985 | |||||||
| chr17:12100033 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.513+4339C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100033 | |||||||
| chr17:12100090 | C | G | 1 | a0001c0001t0002g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.513+4396C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100090 | |||||||
| chr17:12100191 | A | T | 1 | a0001c0001t0001g0033 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.513+4497A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100191 | |||||||
| chr17:12100361 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.513+4667A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100361 | |||||||
| chr17:12100504 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+4810A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100504 | |||||||
| chr17:12100753 | G | A | 1 | a0001c0001t0002g0298 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.513+5059G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100753 | |||||||
| chr17:12100765 | G | A | 8 | a0001c0001t0001g0033 a0001c0001t0001g0100 a0001c0001t0001g0156 others(5): Show |
8 | HG01192.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+5071G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100765 | |||||||
| chr17:12100819 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0047 |
2 | HG00099.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.513+5125T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100819 | |||||||
| chr17:12101005 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.513+5311G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101005 | |||||||
| chr17:12101017 | A | G | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.513+5323A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101017 | |||||||
| chr17:12101440 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.513+5746T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101440 | |||||||
| chr17:12101610 | A | T | 1 | a0001c0001t0001g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.513+5916A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101610 | |||||||
| chr17:12101700 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.513+6006T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101700 | |||||||
| chr17:12101761 | C | T | 40 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0288 others(37): Show |
40 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.514-6029C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101761 | |||||||
| chr17:12101780 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.514-6010T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101780 | |||||||
| chr17:12101934 | A | G | 120 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0101 others(117): Show |
120 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.514-5856A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101934 | |||||||
| chr17:12101957 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.514-5833G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101957 | |||||||
| chr17:12102335 | A | C | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 |
3 | HG01106.hp2 HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.514-5455A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12102335 | |||||||
| chr17:12102336 | T | A | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(3): Show |
6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-5454T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12102336 | |||||||
| chr17:12102361 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.514-5429A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12102361 | |||||||
| chr17:12102463 | C | G | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.514-5327C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12102463 | |||||||
| chr17:12102818 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.514-4972C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12102818 | |||||||
| chr17:12103039 | T | TA | 7 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0096 others(4): Show |
7 | HG00597.hp1 HG01081.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.514-4731dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12103039 | ||||||
| chr17:12103039 | TA | T | 11 | a0001c0001t0001g0147 a0001c0001t0001g0244 a0001c0001t0002g0133 others(8): Show |
11 | HG02559.hp2 HG03139.hp1 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.514-4731delA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12103039 | ||||||
| chr17:12103212 | A | AT | 8 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0004g0042 others(5): Show |
8 | HG00544.hp2 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-4561dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12103212 | ||||||
| chr17:12103350 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.514-4440G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103350 | |||||||
| chr17:12103398 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.514-4392G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103398 | |||||||
| chr17:12103403 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.514-4387G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103403 | |||||||
| chr17:12103463 | G | A | 17 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0001t0002g0260 others(14): Show |
17 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.514-4327G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103463 | |||||||
| chr17:12103475 | A | T | 1 | a0001c0001t0001g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.514-4315A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103475 | |||||||
| chr17:12103697 | T | C | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.514-4093T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103697 | |||||||
| chr17:12103720 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0022 |
3 | HG02055.hp1 HG02647.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.514-4070G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103720 | |||||||
| chr17:12103762 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(4): Show |
7 | HG02055.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.514-4028C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103762 | |||||||
| chr17:12103826 | A | G | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.514-3964A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103826 | |||||||
| chr17:12104326 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.514-3464A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12104326 | |||||||
| chr17:12104516 | C | T | 2 | a0001c0001t0001g0276 a0002c0004t0012g0027 |
2 | HG01243.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.514-3274C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12104516 | |||||||
| chr17:12104565 | A | T | 4 | a0001c0001t0001g0188 a0001c0001t0001g0212 a0001c0001t0002g0275 others(1): Show |
4 | HG02015.hp2 HG03669.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-3225A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12104565 | |||||||
| chr17:12104579 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.514-3211T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12104579 | |||||||
| chr17:12104621 | T | C | 1 | a0001c0001t0003g0067 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.514-3169T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12104621 | |||||||
| chr17:12104625 | A | G | 2 | a0001c0001t0004g0289 a0001c0001t0004g0290 |
2 | HG02132.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.514-3165A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12104625 | |||||||
| chr17:12104690 | C | T | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.514-3100C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12104690 | |||||||
| chr17:12105376 | C | T | 6 | a0001c0001t0001g0273 a0001c0001t0001g0277 a0001c0001t0001g0281 others(3): Show |
6 | HG02055.hp2 HG02451.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-2414C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12105376 | |||||||
| chr17:12105445 | C | T | 1 | a0001c0001t0011g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.514-2345C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12105445 | |||||||
| chr17:12105542 | T | A | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-2248T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12105542 | |||||||
| chr17:12105548 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.514-2242T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12105548 | |||||||
| chr17:12105581 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.514-2209T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12105581 | |||||||
| chr17:12106568 | A | G | 3 | a0001c0001t0002g0232 a0001c0001t0002g0251 a0001c0001t0002g0252 |
3 | HG02818.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.514-1222A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12106568 | |||||||
| chr17:12106678 | C | T | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.514-1112C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12106678 | |||||||
| chr17:12106686 | A | G | 2 | a0001c0001t0001g0235 a0001c0001t0016g0234 |
2 | HG00639.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.514-1104A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12106686 | |||||||
| chr17:12106888 | T | C | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.514-902T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12106888 | |||||||
| chr17:12106914 | A | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(50): Show |
56 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.514-876A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12106914 | |||||||
| chr17:12106941 | T | C | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.514-849T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12106941 | |||||||
| chr17:12106958 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0021 others(1): Show |
4 | HG02809.hp2 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-832T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12106958 | |||||||
| chr17:12107220 | A | G | 3 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02970.hp2 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.514-570A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12107220 | |||||||
| chr17:12107363 | A | G | 180 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(177): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.514-427A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12107363 | |||||||
| chr17:12107382 | C | CT | 18 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0108 others(15): Show |
18 | HG00280.hp1 HG00558.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.514-389dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12107382 | ||||||
| chr17:12107382 | C | CTT | 8 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0127 others(5): Show |
8 | HG00609.hp2 HG00621.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.514-390_514-389dup others(2): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12107382 | ||||||
| chr17:12107488 | A | T | 1 | a0001c0001t0002g0251 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.514-302A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12107488 | |||||||
| chr17:12107629 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.514-161T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12107629 | |||||||
| chr17:12107969 | A | G | 1 | a0001c0001t0001g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.633+60A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12107969 | |||||||
| chr17:12108089 | C | T | 3 | a0001c0001t0002g0232 a0001c0001t0002g0251 a0001c0001t0002g0252 |
3 | HG02818.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.633+180C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12108089 | |||||||
| chr17:12108557 | T | TTTGTA | 112 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(109): Show |
112 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.633+648_633+649ins others(5): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12108557 | |||||||
| chr17:12108591 | T | G | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.633+682T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12108591 | |||||||
| chr17:12108802 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.633+893A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12108802 | |||||||
| chr17:12108877 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.633+968A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12108877 | |||||||
| chr17:12108981 | A | C | 1 | a0001c0001t0001g0140 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.633+1072A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12108981 | |||||||
| chr17:12109215 | G | A | 1 | a0001c0001t0002g0318 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.634-1160G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12109215 | |||||||
| chr17:12109350 | A | G | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.634-1025A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12109350 | |||||||
| chr17:12109379 | A | G | 265 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(262): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.634-996A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12109379 | |||||||
| chr17:12109488 | G | A | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.634-887G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12109488 | |||||||
| chr17:12109612 | G | C | 1 | a0001c0001t0002g0132 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.634-763G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12109612 | |||||||
| chr17:12109954 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.634-421C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12109954 | |||||||
| chr17:12109967 | A | C | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG01934.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.634-408A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12109967 | |||||||
| chr17:12110042 | G | C | 1 | a0001c0001t0003g0112 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.634-333G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12110042 | |||||||
| chr17:12110210 | T | C | 3 | a0001c0001t0002g0232 a0001c0001t0002g0251 a0001c0001t0002g0252 |
3 | HG02818.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.634-165T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12110210 | |||||||
| chr17:12110291 | C | A | 1 | a0001c0001t0002g0298 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.634-84C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12110291 | |||||||
| chr17:12110291 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.634-84C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12110291 | |||||||
| chr17:12110304 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.634-71G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12110304 | |||||||
| chr17:12110311 | A | G | 1 | a0001c0001t0003g0112 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.634-64A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12110311 | |||||||
| chr17:12110487 | C | T | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.685+61C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12110487 | |||||||
| chr17:12110776 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.685+350A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12110776 | |||||||
| chr17:12111375 | T | C | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.685+949T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111375 | |||||||
| chr17:12111468 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.685+1042G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111468 | |||||||
| chr17:12111493 | T | C | 6 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0242 others(3): Show |
6 | HG02083.hp1 NA18945.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.685+1067T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111493 | |||||||
| chr17:12111658 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.685+1232A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111658 | |||||||
| chr17:12111782 | G | T | 4 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG02055.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.685+1356G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111782 | |||||||
| chr17:12111834 | A | AATATGAC | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(2): Show |
5 | HG02145.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.686-1399_686-1398i others(9): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111834 | |||||||
| chr17:12111836 | A | AGGGGTCA others(3): Show |
5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(2): Show |
5 | HG02145.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.686-1397_686-1396i others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111836 | |||||||
| chr17:12111836 | A | ATCACTAG others(9): Show |
1 | a0002c0004t0012g0027 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.686-1396_686-1395i others(18): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 12111836 | ||||||
| chr17:12111836 | A | ATGACTAG others(9): Show |
285 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(282): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.686-1395_686-1394i others(18): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 12111836 | ||||||
| chr17:12111980 | T | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0021 others(1): Show |
4 | HG02809.hp2 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.686-1253T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111980 | |||||||
| chr17:12111995 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.686-1238C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111995 | |||||||
| chr17:12112053 | C | G | 1 | a0001c0001t0001g0050 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.686-1180C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12112053 | |||||||
| chr17:12112228 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.686-1005C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12112228 | |||||||
| chr17:12112235 | G | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.686-998G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12112235 | |||||||
| chr17:12112332 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.686-901G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12112332 | |||||||
| chr17:12112388 | G | C | 1 | a0001c0001t0001g0009 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.686-845G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12112388 | |||||||
| chr17:12112409 | G | T | 2 | a0001c0001t0001g0276 a0002c0004t0012g0027 |
2 | HG01243.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.686-824G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12112409 | |||||||
| chr17:12112442 | A | G | 1 | a0001c0001t0002g0287 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.686-791A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12112442 | |||||||
| chr17:12112465 | C | CA | 138 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0034 others(135): Show |
139 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.686-748dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 12112465 | ||||||
| chr17:12112465 | C | CAA | 6 | a0001c0001t0001g0179 a0001c0001t0001g0238 a0001c0001t0001g0273 others(3): Show |
6 | HG01243.hp1 HG01934.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.686-749_686-748dup others(2): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 12112465 | ||||||
| chr17:12113371 | A | G | 2 | a0001c0001t0004g0230 a0001c0001t0004g0231 |
2 | NA18995.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.813+11A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12113371 | |||||||
| chr17:12113442 | C | T | 8 | a0001c0001t0002g0132 a0001c0001t0002g0255 a0001c0001t0002g0303 others(5): Show |
8 | HG00544.hp1 HG00673.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.813+82C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12113442 | |||||||
| chr17:12113731 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0166 |
2 | HG02258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.813+371A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12113731 | |||||||
| chr17:12114128 | G | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(261): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.813+768G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12114128 | |||||||
| chr17:12114387 | G | GGT | 33 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(30): Show |
33 | HG01106.hp1 HG01891.hp1 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.813+1056_813+1057d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12114387 | ||||||
| chr17:12114387 | G | GGTGT | 8 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(5): Show |
8 | HG02055.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.813+1054_813+1057d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12114387 | ||||||
| chr17:12114387 | G | GGTGTGTG others(5): Show |
1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.813+1046_813+1057d others(14): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12114387 | ||||||
| chr17:12114387 | GGT | G | 174 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(171): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.813+1056_813+1057d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12114387 | ||||||
| chr17:12114387 | GGTGTGTG others(7): Show |
G | 71 | a0001c0001t0001g0256 a0001c0001t0001g0272 a0001c0001t0001g0273 others(68): Show |
71 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.813+1044_813+1057d others(16): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12114387 | ||||||
| chr17:12114517 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.813+1157T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12114517 | |||||||
| chr17:12114631 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | NA18970.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.813+1271A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12114631 | |||||||
| chr17:12114672 | G | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.813+1312G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12114672 | |||||||
| chr17:12114828 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.813+1468T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12114828 | |||||||
| chr17:12114872 | G | A | 1 | a0001c0001t0002g0298 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.813+1512G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12114872 | |||||||
| chr17:12114971 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.813+1611C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12114971 | |||||||
| chr17:12115090 | C | A | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.813+1730C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115090 | |||||||
| chr17:12115230 | C | T | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.813+1870C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115230 | |||||||
| chr17:12115264 | T | C | 1 | a0001c0001t0004g0230 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.813+1904T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115264 | |||||||
| chr17:12115311 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.813+1951A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115311 | |||||||
| chr17:12115520 | G | A | 8 | a0001c0001t0001g0121 a0001c0001t0001g0127 a0001c0001t0001g0128 others(5): Show |
8 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.813+2160G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115520 | |||||||
| chr17:12115533 | C | T | 1 | a0001c0001t0002g0317 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.813+2173C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115533 | |||||||
| chr17:12115534 | G | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.813+2174G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115534 | |||||||
| chr17:12115538 | C | T | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.813+2178C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115538 | |||||||
| chr17:12115878 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.813+2518T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115878 | |||||||
| chr17:12115975 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.813+2615T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115975 | |||||||
| chr17:12116076 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.813+2716C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116076 | |||||||
| chr17:12116265 | T | C | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.813+2905T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116265 | |||||||
| chr17:12116438 | TAATA | T | 4 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG02055.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.813+3082_813+3085d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12116438 | ||||||
| chr17:12116499 | A | T | 3 | a0001c0001t0001g0288 a0001c0001t0001g0292 a0001c0001t0001g0293 |
3 | HG00280.hp2 HG02257.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.813+3139A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116499 | |||||||
| chr17:12116500 | T | A | 1 | a0001c0001t0002g0267 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.813+3140T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116500 | |||||||
| chr17:12116553 | AG | A | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.813+3194delG | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116553 | |||||||
| chr17:12116557 | G | A | 1 | a0001c0001t0002g0133 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.813+3197G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116557 | |||||||
| chr17:12116771 | A | G | 62 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(59): Show |
65 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.813+3411A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116771 | |||||||
| chr17:12116773 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.813+3413G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116773 | |||||||
| chr17:12117171 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(62): Show |
68 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.813+3811C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12117171 | |||||||
| chr17:12117276 | G | A | 2 | a0001c0001t0007g0248 a0001c0001t0007g0249 |
2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.813+3916G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12117276 | |||||||
| chr17:12117317 | G | A | 2 | a0001c0001t0007g0248 a0001c0001t0007g0249 |
2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.813+3957G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12117317 | |||||||
| chr17:12117409 | TA | T | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(3): Show |
6 | HG02165.hp2 NA18970.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.813+4060delA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12117409 | ||||||
| chr17:12117509 | A | C | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.813+4149A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12117509 | |||||||
| chr17:12117597 | AT | A | 196 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(193): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.813+4246delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12117597 | ||||||
| chr17:12117608 | T | G | 3 | a0001c0001t0001g0140 a0001c0001t0003g0032 a0001c0001t0003g0079 |
3 | NA18983.hp2 NA18997.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.813+4248T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12117608 | |||||||
| chr17:12117810 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.813+4450G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12117810 | |||||||
| chr17:12117953 | G | A | 1 | a0001c0001t0004g0165 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.813+4593G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12117953 | |||||||
| chr17:12118230 | T | C | 83 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(80): Show |
86 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.813+4870T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12118230 | |||||||
| chr17:12118263 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.813+4903C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12118263 | |||||||
| chr17:12118348 | G | A | 2 | a0001c0001t0002g0316 a0001c0001t0014g0090 |
2 | HG01975.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.813+4988G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12118348 | |||||||
| chr17:12118447 | G | A | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.813+5087G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12118447 | |||||||
| chr17:12118489 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.813+5129T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12118489 | |||||||
| chr17:12118779 | A | T | 1 | a0001c0001t0001g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.813+5419A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12118779 | |||||||
| chr17:12118893 | G | A | 4 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG01123.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.813+5533G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12118893 | |||||||
| chr17:12119001 | G | A | 1 | a0001c0001t0005g0186 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.813+5641G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119001 | |||||||
| chr17:12119249 | T | C | 285 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(282): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.813+5889T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119249 | |||||||
| chr17:12119265 | A | G | 5 | a0001c0001t0003g0002 a0001c0001t0003g0031 a0001c0001t0003g0054 others(2): Show |
6 | HG00621.hp1 NA18943.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.813+5905A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119265 | |||||||
| chr17:12119404 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.814-5890G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119404 | |||||||
| chr17:12119437 | G | A | 1 | a0001c0001t0003g0069 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.814-5857G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119437 | |||||||
| chr17:12119476 | T | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.814-5818T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119476 | |||||||
| chr17:12119559 | A | G | 1 | a0001c0001t0004g0044 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.814-5735A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119559 | |||||||
| chr17:12119583 | C | A | 2 | a0001c0001t0001g0156 a0001c0001t0018g0046 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.814-5711C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119583 | |||||||
| chr17:12119588 | A | G | 2 | a0001c0001t0001g0156 a0001c0001t0018g0046 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.814-5706A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119588 | |||||||
| chr17:12119616 | C | T | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.814-5678C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119616 | |||||||
| chr17:12119870 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.814-5424A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119870 | |||||||
| chr17:12120044 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0278 |
2 | HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.814-5250A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12120044 | |||||||
| chr17:12120186 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(78): Show |
84 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.814-5108C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12120186 | |||||||
| chr17:12120188 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.814-5106C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12120188 | |||||||
| chr17:12120227 | A | G | 65 | a0001c0001t0001g0274 a0001c0001t0001g0278 a0001c0001t0002g0056 others(62): Show |
65 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.814-5067A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12120227 | |||||||
| chr17:12120534 | T | TC | 260 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(257): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.814-4751dupC | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12120534 | ||||||
| chr17:12120738 | T | G | 1 | a0001c0001t0001g0173 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.814-4556T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12120738 | |||||||
| chr17:12121030 | C | G | 61 | a0001c0001t0001g0209 a0001c0001t0002g0056 a0001c0001t0002g0057 others(58): Show |
61 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.814-4264C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121030 | |||||||
| chr17:12121039 | G | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.814-4255G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121039 | |||||||
| chr17:12121058 | G | A | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(3): Show |
6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.814-4236G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121058 | |||||||
| chr17:12121166 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(193): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.814-4128A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121166 | |||||||
| chr17:12121169 | T | A | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.814-4125T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121169 | |||||||
| chr17:12121205 | T | C | 1 | a0001c0001t0002g0300 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.814-4089T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121205 | |||||||
| chr17:12121418 | T | C | 4 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(1): Show |
4 | HG01106.hp2 HG02683.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.814-3876T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121418 | |||||||
| chr17:12121532 | G | A | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.814-3762G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121532 | |||||||
| chr17:12121574 | C | CA | 70 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0120 others(67): Show |
70 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.814-3700dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12121574 | ||||||
| chr17:12121574 | C | CAA | 9 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(6): Show |
9 | HG01261.hp2 HG02109.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.814-3701_814-3700d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12121574 | ||||||
| chr17:12121574 | CA | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0030 others(71): Show |
76 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.814-3700delA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12121574 | ||||||
| chr17:12121574 | CAA | C | 6 | a0001c0001t0003g0002 a0001c0001t0003g0031 a0001c0001t0003g0054 others(3): Show |
7 | HG00621.hp1 NA18943.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.814-3701_814-3700d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12121574 | ||||||
| chr17:12121687 | T | C | 1 | a0001c0001t0002g0266 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.814-3607T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121687 | |||||||
| chr17:12121725 | G | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0100 a0001c0001t0001g0157 others(2): Show |
5 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.814-3569G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121725 | |||||||
| chr17:12121735 | G | C | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.814-3559G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121735 | |||||||
| chr17:12121892 | G | C | 266 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(263): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.814-3402G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121892 | |||||||
| chr17:12121944 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0001g0278 |
2 | HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.814-3350T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121944 | |||||||
| chr17:12121958 | G | A | 1 | a0001c0001t0002g0310 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.814-3336G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121958 | |||||||
| chr17:12121996 | A | G | 2 | a0001c0001t0001g0273 a0001c0001t0001g0277 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.814-3298A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121996 | |||||||
| chr17:12122133 | C | T | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(3): Show |
6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.814-3161C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12122133 | |||||||
| chr17:12122556 | T | A | 1 | a0001c0001t0019g0295 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.814-2738T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12122556 | |||||||
| chr17:12122679 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.814-2615A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12122679 | |||||||
| chr17:12122738 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG01106.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.814-2556A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12122738 | |||||||
| chr17:12122764 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.814-2530A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12122764 | |||||||
| chr17:12122790 | A | G | 2 | a0001c0001t0002g0301 a0001c0001t0002g0311 |
2 | NA18950.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.814-2504A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12122790 | |||||||
| chr17:12123033 | T | A | 1 | a0001c0001t0004g0044 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.814-2261T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123033 | |||||||
| chr17:12123142 | C | T | 17 | a0001c0001t0004g0026 a0001c0001t0004g0029 a0001c0001t0004g0035 others(14): Show |
17 | HG00673.hp2 HG01891.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.814-2152C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123142 | |||||||
| chr17:12123201 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.814-2093G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123201 | |||||||
| chr17:12123315 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.814-1979T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123315 | |||||||
| chr17:12123593 | C | CT | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.814-1693dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12123593 | ||||||
| chr17:12123617 | A | G | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(3): Show |
6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.814-1677A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123617 | |||||||
| chr17:12123745 | A | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.814-1549A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123745 | |||||||
| chr17:12123795 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.814-1499G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123795 | |||||||
| chr17:12123891 | G | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0019 others(3): Show |
6 | HG02109.hp2 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.814-1403G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123891 | |||||||
| chr17:12123919 | G | A | 1 | a0001c0001t0002g0232 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.814-1375G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123919 | |||||||
| chr17:12124077 | C | CA | 5 | a0001c0001t0001g0033 a0001c0001t0001g0100 a0001c0001t0001g0157 others(2): Show |
5 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.814-1208dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12124077 | ||||||
| chr17:12124077 | CA | C | 206 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.814-1208delA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12124077 | ||||||
| chr17:12124279 | G | A | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.814-1015G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12124279 | |||||||
| chr17:12124283 | C | T | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(3): Show |
6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.814-1011C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12124283 | |||||||
| chr17:12124367 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG01123.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.814-927T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12124367 | |||||||
| chr17:12124565 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.814-729T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12124565 | |||||||
| chr17:12124884 | C | G | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.814-410C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12124884 | |||||||
| chr17:12124911 | C | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.814-383C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12124911 | |||||||
| chr17:12125048 | C | G | 1 | a0001c0001t0001g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.814-246C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12125048 | |||||||
| chr17:12125267 | T | G | 1 | a0001c0001t0002g0135 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.814-27T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12125267 | |||||||
| chr17:12125473 | A | G | 2 | a0001c0001t0001g0156 a0001c0001t0018g0046 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.891+102A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12125473 | |||||||
| chr17:12125540 | A | C | 1 | a0002c0004t0012g0027 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.891+169A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12125540 | |||||||
| chr17:12125675 | C | T | 3 | a0001c0001t0003g0067 a0001c0001t0003g0085 a0001c0001t0003g0112 |
3 | HG00558.hp2 HG00609.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.891+304C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12125675 | |||||||
| chr17:12125911 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.891+540C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12125911 | |||||||
| chr17:12125950 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.891+579A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12125950 | |||||||
| chr17:12126157 | G | A | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.891+786G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126157 | |||||||
| chr17:12126572 | G | A | 1 | a0001c0001t0002g0106 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.891+1201G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126572 | |||||||
| chr17:12126575 | G | A | 4 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG02055.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+1204G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126575 | |||||||
| chr17:12126611 | G | T | 1 | a0001c0001t0001g0007 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.891+1240G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126611 | |||||||
| chr17:12126771 | T | C | 5 | a0001c0001t0004g0038 a0001c0001t0004g0155 a0001c0001t0004g0289 others(2): Show |
5 | HG00673.hp2 HG02040.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+1400T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126771 | |||||||
| chr17:12126773 | G | C | 2 | a0001c0001t0002g0135 a0001c0001t0002g0304 |
2 | NA18977.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.891+1402G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126773 | |||||||
| chr17:12126871 | C | T | 1 | a0001c0001t0002g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.891+1500C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126871 | |||||||
| chr17:12126973 | C | G | 2 | a0001c0001t0002g0287 a0001c0001t0002g0291 |
2 | NA18966.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.891+1602C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126973 | |||||||
| chr17:12127160 | A | G | 1 | a0001c0003t0001g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.891+1789A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127160 | |||||||
| chr17:12127300 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.892-1839G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127300 | |||||||
| chr17:12127333 | G | C | 1 | a0001c0001t0001g0034 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.892-1806G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127333 | |||||||
| chr17:12127464 | A | C | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-1675A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127464 | |||||||
| chr17:12127792 | C | T | 195 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.892-1347C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127792 | |||||||
| chr17:12127830 | G | A | 65 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(62): Show |
68 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.892-1309G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127830 | |||||||
| chr17:12127847 | CAT | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0053 a0001c0001t0001g0104 |
3 | HG02027.hp1 HG02071.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.892-1291_892-1290d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127847 | |||||||
| chr17:12127884 | G | T | 1 | a0001c0001t0002g0313 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.892-1255G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127884 | |||||||
| chr17:12128027 | C | T | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.892-1112C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128027 | |||||||
| chr17:12128164 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.892-975G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128164 | |||||||
| chr17:12128279 | G | A | 2 | a0001c0001t0002g0058 a0001c0001t0002g0264 |
2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.892-860G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128279 | |||||||
| chr17:12128323 | C | T | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.892-816C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128323 | |||||||
| chr17:12128324 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.892-815G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128324 | |||||||
| chr17:12128346 | G | C | 2 | a0001c0001t0001g0156 a0001c0001t0018g0046 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.892-793G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128346 | |||||||
| chr17:12128386 | G | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(2): Show |
5 | HG02486.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-753G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128386 | |||||||
| chr17:12128457 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.892-682T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128457 | |||||||
| chr17:12128491 | G | A | 1 | a0001c0001t0004g0041 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.892-648G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128491 | |||||||
| chr17:12128608 | G | C | 4 | a0001c0001t0002g0072 a0001c0001t0002g0261 a0001c0001t0002g0266 others(1): Show |
4 | HG00639.hp2 HG02602.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.892-531G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128608 | |||||||
| chr17:12128825 | T | A | 1 | a0001c0001t0001g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.892-314T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128825 | |||||||
| chr17:12128870 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.892-269G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128870 | |||||||
| chr17:12129030 | A | G | 3 | a0001c0001t0007g0025 a0001c0001t0007g0248 a0001c0001t0007g0249 |
3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.892-109A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12129030 | |||||||
| chr17:12129304 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1040+17T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12129304 | |||||||
| chr17:12129325 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0168 |
2 | HG02630.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1040+38C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12129325 | |||||||
| chr17:12129537 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1040+250T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12129537 | |||||||
| chr17:12129622 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1040+335A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12129622 | |||||||
| chr17:12129627 | A | G | 61 | a0001c0001t0001g0209 a0001c0001t0002g0056 a0001c0001t0002g0057 others(58): Show |
61 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1040+340A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12129627 | |||||||
| chr17:12130382 | T | G | 1 | a0001c0001t0005g0196 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1040+1095T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12130382 | |||||||
| chr17:12130619 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1040+1332T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12130619 | |||||||
| chr17:12130835 | A | G | 3 | a0001c0001t0001g0274 a0001c0001t0001g0278 a0002c0004t0012g0027 |
3 | HG01243.hp2 HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1040+1548A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12130835 | |||||||
| chr17:12130946 | A | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0288 |
2 | HG03239.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1040+1659A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12130946 | |||||||
| chr17:12130970 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1040+1683G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12130970 | |||||||
| chr17:12131143 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1040+1856A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131143 | |||||||
| chr17:12131200 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(2): Show |
5 | HG02486.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1040+1913G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131200 | |||||||
| chr17:12131209 | T | C | 1 | a0001c0001t0005g0307 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1040+1922T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131209 | |||||||
| chr17:12131234 | CT | C | 121 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(118): Show |
121 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.1040+1964delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12131234 | ||||||
| chr17:12131271 | A | G | 1 | a0001c0001t0002g0317 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1040+1984A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131271 | |||||||
| chr17:12131289 | A | G | 4 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG02055.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040+2002A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131289 | |||||||
| chr17:12131492 | G | T | 1 | a0001c0001t0001g0241 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1040+2205G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131492 | |||||||
| chr17:12131546 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0018g0046 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1040+2259G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131546 | |||||||
| chr17:12131636 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1040+2349G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131636 | |||||||
| chr17:12131959 | G | A | 28 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(25): Show |
28 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1040+2672G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131959 | |||||||
| chr17:12132190 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1040+2903T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12132190 | |||||||
| chr17:12132351 | A | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0100 a0001c0001t0001g0176 others(1): Show |
4 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1040+3064A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12132351 | |||||||
| chr17:12132362 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1040+3075G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12132362 | |||||||
| chr17:12132436 | C | G | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1040+3149C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12132436 | |||||||
| chr17:12132608 | AG | A | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(3): Show |
6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040+3323delG | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12132608 | ||||||
| chr17:12132610 | G | GA | 11 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0014 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1040+3335dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12132610 | ||||||
| chr17:12132658 | C | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0100 a0001c0001t0001g0176 |
3 | HG01192.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1040+3371C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12132658 | |||||||
| chr17:12132702 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1040+3415G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12132702 | |||||||
| chr17:12132760 | TAGAA | T | 28 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(25): Show |
28 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1040+3480_1040+348 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12132760 | ||||||
| chr17:12132776 | T | G | 1 | a0001c0001t0018g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1040+3489T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12132776 | |||||||
| chr17:12133027 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1040+3740A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133027 | |||||||
| chr17:12133070 | T | TTTG | 6 | a0001c0001t0001g0009 a0001c0001t0001g0156 a0001c0001t0001g0198 others(3): Show |
6 | HG02165.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1040+3807_1040+380 others(7): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12133070 | ||||||
| chr17:12133185 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1040+3898G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133185 | |||||||
| chr17:12133285 | C | G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+3998C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133285 | |||||||
| chr17:12133328 | C | T | 2 | a0001c0001t0003g0067 a0001c0001t0003g0112 |
2 | HG00558.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.1040+4041C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133328 | |||||||
| chr17:12133343 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4056G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133343 | |||||||
| chr17:12133345 | G | A | 3 | a0001c0001t0008g0189 a0001c0001t0008g0191 a0001c0001t0008g0192 |
3 | NA18990.hp1 NA19054.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1040+4058G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133345 | |||||||
| chr17:12133362 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4075G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133362 | |||||||
| chr17:12133363 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1040+4076T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133363 | |||||||
| chr17:12133430 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4143T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133430 | |||||||
| chr17:12133500 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1040+4213C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133500 | |||||||
| chr17:12133554 | C | G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4267C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133554 | |||||||
| chr17:12133606 | ATT | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4326_1040+432 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12133606 | ||||||
| chr17:12133643 | G | GA | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(3): Show |
6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040+4356_1040+435 others(5): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133643 | |||||||
| chr17:12133644 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4357G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133644 | |||||||
| chr17:12133647 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4360G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133647 | |||||||
| chr17:12133733 | C | A | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1040+4446C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133733 | |||||||
| chr17:12133771 | C | G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4484C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133771 | |||||||
| chr17:12133777 | C | G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4490C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133777 | |||||||
| chr17:12133999 | A | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1040+4712A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133999 | |||||||
| chr17:12134063 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4776T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134063 | |||||||
| chr17:12134084 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1040+4797A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134084 | |||||||
| chr17:12134096 | A | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1040+4809A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134096 | |||||||
| chr17:12134108 | G | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4821G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134108 | |||||||
| chr17:12134190 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1040+4903C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134190 | |||||||
| chr17:12134208 | C | G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4921C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134208 | |||||||
| chr17:12134295 | C | CCTAT | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+5011_1040+501 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12134295 | ||||||
| chr17:12134491 | C | T | 82 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(79): Show |
82 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.1040+5204C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134491 | |||||||
| chr17:12134492 | G | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+5205G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134492 | |||||||
| chr17:12134545 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1040+5258G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134545 | |||||||
| chr17:12134599 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-5240T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134599 | |||||||
| chr17:12134653 | A | G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-5186A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134653 | |||||||
| chr17:12134701 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-5138G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134701 | |||||||
| chr17:12134735 | A | G | 198 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(195): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1041-5104A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134735 | |||||||
| chr17:12134751 | A | C | 1 | a0001c0001t0004g0044 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1041-5088A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134751 | |||||||
| chr17:12134824 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-5015T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134824 | |||||||
| chr17:12134949 | C | A | 6 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0299 others(3): Show |
6 | HG00597.hp1 NA18612.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1041-4890C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134949 | |||||||
| chr17:12134969 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-4870T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134969 | |||||||
| chr17:12135002 | A | T | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1041-4837A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135002 | |||||||
| chr17:12135065 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1041-4774G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135065 | |||||||
| chr17:12135075 | G | GT | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-4757dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12135075 | ||||||
| chr17:12135151 | T | G | 1 | a0001c0001t0001g0138 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1041-4688T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135151 | |||||||
| chr17:12135158 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1041-4681G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135158 | |||||||
| chr17:12135198 | C | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-4641C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135198 | |||||||
| chr17:12135258 | T | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0294 |
2 | NA18949.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1041-4581T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135258 | |||||||
| chr17:12135327 | G | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041-4512G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135327 | |||||||
| chr17:12135335 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1041-4504C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135335 | |||||||
| chr17:12135460 | A | T | 1 | a0001c0001t0009g0001 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1041-4379A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135460 | |||||||
| chr17:12135484 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0011g0017 |
3 | HG02145.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1041-4355G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135484 | |||||||
| chr17:12135491 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1041-4348C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135491 | |||||||
| chr17:12135697 | G | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-4142G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135697 | |||||||
| chr17:12135746 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-4093T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135746 | |||||||
| chr17:12135770 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-4069G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135770 | |||||||
| chr17:12136103 | C | T | 1 | a0001c0001t0003g0061 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1041-3736C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136103 | |||||||
| chr17:12136406 | A | G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-3433A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136406 | |||||||
| chr17:12136584 | G | T | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-3255G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136584 | |||||||
| chr17:12136650 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-3189G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136650 | |||||||
| chr17:12136669 | AAAAG | A | 103 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(100): Show |
103 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1041-3167_1041-316 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12136669 | ||||||
| chr17:12136671 | A | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-3168A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136671 | |||||||
| chr17:12136680 | G | T | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(3): Show |
6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1041-3159G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136680 | |||||||
| chr17:12136715 | G | A | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041-3124G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136715 | |||||||
| chr17:12136754 | G | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-3085G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136754 | |||||||
| chr17:12136872 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-2967T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136872 | |||||||
| chr17:12136877 | TG | T | 5 | a0001c0001t0002g0132 a0001c0001t0002g0255 a0001c0001t0002g0303 others(2): Show |
5 | HG00544.hp1 HG02015.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1041-2960delG | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12136877 | ||||||
| chr17:12137438 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-2401T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12137438 | |||||||
| chr17:12137552 | G | A | 1 | a0001c0001t0002g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1041-2287G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12137552 | |||||||
| chr17:12137610 | A | G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-2229A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12137610 | |||||||
| chr17:12137734 | A | G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-2105A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12137734 | |||||||
| chr17:12137781 | CAA | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-2056_1041-205 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12137781 | ||||||
| chr17:12137825 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0137 |
2 | NA18943.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1041-2014T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12137825 | |||||||
| chr17:12137866 | A | AATG | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-1970_1041-196 others(7): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12137866 | ||||||
| chr17:12137871 | TAAAC | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041-1964_1041-196 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12137871 | ||||||
| chr17:12138007 | G | A | 65 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0002g0056 others(62): Show |
65 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1041-1832G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138007 | |||||||
| chr17:12138176 | T | G | 1 | a0001c0001t0006g0111 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1041-1663T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138176 | |||||||
| chr17:12138200 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-1639T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138200 | |||||||
| chr17:12138231 | A | AGGTTAGG others(16): Show |
8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-1607_1041-158 others(27): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12138231 | ||||||
| chr17:12138232 | G | A | 4 | a0001c0001t0004g0155 a0001c0001t0004g0289 a0001c0001t0004g0290 others(1): Show |
4 | HG00673.hp2 HG02132.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.1041-1607G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138232 | |||||||
| chr17:12138316 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1041-1523T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138316 | |||||||
| chr17:12138344 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0023 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1041-1495C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138344 | |||||||
| chr17:12138447 | ATATAT | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-1388_1041-138 others(9): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12138447 | ||||||
| chr17:12138471 | G | A | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(3): Show |
6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1041-1368G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138471 | |||||||
| chr17:12138557 | A | G | 9 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(6): Show |
9 | HG02165.hp2 HG02622.hp1 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1041-1282A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138557 | |||||||
| chr17:12138691 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1041-1148G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138691 | |||||||
| chr17:12138712 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1041-1127G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138712 | |||||||
| chr17:12138777 | G | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0021 others(3): Show |
6 | HG01243.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1041-1062G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138777 | |||||||
| chr17:12138791 | A | G | 1 | a0001c0001t0002g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1041-1048A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138791 | |||||||
| chr17:12138846 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1041-993G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138846 | |||||||
| chr17:12139050 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-789T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139050 | |||||||
| chr17:12139247 | A | G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-592A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139247 | |||||||
| chr17:12139307 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-532T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139307 | |||||||
| chr17:12139315 | T | C | 89 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(86): Show |
92 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1041-524T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139315 | |||||||
| chr17:12139460 | A | G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-379A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139460 | |||||||
| chr17:12139534 | CATTT | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-302_1041-299d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12139534 | ||||||
| chr17:12139617 | T | A | 65 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0002g0056 others(62): Show |
65 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1041-222T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139617 | |||||||
| chr17:12139697 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1041-142G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139697 | |||||||
| chr17:12139738 | G | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-101G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139738 | |||||||
| chr17:12139977 | C | T | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1086+93C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12139977 | |||||||
| chr17:12139995 | A | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1086+111A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12139995 | |||||||
| chr17:12140136 | A | T | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(3): Show |
6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1086+252A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140136 | |||||||
| chr17:12140162 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1086+278A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140162 | |||||||
| chr17:12140214 | A | AG | 288 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(285): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1086+330_1086+331i others(3): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140214 | |||||||
| chr17:12140256 | G | A | 269 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(266): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1086+372G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140256 | |||||||
| chr17:12140301 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1086+417A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140301 | |||||||
| chr17:12140338 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0250 |
2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1086+454G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140338 | |||||||
| chr17:12140342 | T | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1086+458T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140342 | |||||||
| chr17:12140460 | A | G | 63 | a0001c0001t0001g0104 a0001c0001t0002g0056 a0001c0001t0002g0057 others(60): Show |
63 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1086+576A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140460 | |||||||
| chr17:12140532 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-615G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140532 | |||||||
| chr17:12140772 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-375T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140772 | |||||||
| chr17:12140810 | G | T | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-337G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140810 | |||||||
| chr17:12140832 | G | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-315G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140832 | |||||||
| chr17:12140865 | T | G | 1 | a0001c0001t0001g0226 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1087-282T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140865 | |||||||
| chr17:12140892 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-255G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140892 | |||||||
| chr17:12140928 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-219G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140928 | |||||||
| chr17:12141036 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-111T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12141036 | |||||||
| chr17:12141066 | T | C | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(1): Show |
4 | HG02145.hp1 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1087-81T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12141066 | |||||||
| chr17:12141067 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1087-80A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12141067 |