Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5604 |
| ensemblid | ENSG00000169032.11 |
| hgncid | 6840 |
| symbol | MAP2K1 |
| name | mitogen-activated protein kinase kinase 1 |
| refseq_nuc | NM_002755.4 |
| refseq_prot | NP_002746.1 |
| ensembl_nuc | ENST00000307102.10 |
| ensembl_prot | ENSP00000302486.5 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 66386912 |
| end | 66491544 |
| strand | + |
| ver | v1.2 |
| region | chr15:66386912-66491544 |
| region5000 | chr15:66381912-66496544 |
| regionname0 | MAP2K1_chr15_66386912_66491544 |
| regionname5000 | MAP2K1_chr15_66381912_66496544 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1179 | 367 | 89 | 72 | 150 | 16 | 38 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | ATGCC others(1174): Show |
chr15 | 66381912 | 66496544 | ||
| a0001c0002 | 0/0 | 1179 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | ATGCC others(1174): Show |
chr15 | 66381912 | 66496544 | ||
| a0001c0003 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | ATGCC others(1174): Show |
chr15 | 66381912 | 66496544 | ||
| a0001c0004 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | ATGCC others(1174): Show |
chr15 | 66381912 | 66496544 | ||
| a0001c0005 | 0/0 | 1179 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | ATGCC others(1174): Show |
chr15 | 66381912 | 66496544 | ||
| a0001c0006 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | ATGCC others(1174): Show |
chr15 | 66381912 | 66496544 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2547 | 213 | 74 | 49 | 69 | 2 | 18 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2542): Show |
chr15 | 66381912 | 66496544 |
| a0001c0001t0002 | 0/0 | 2548 | 58 | 6 | 5 | 40 | 3 | 4 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2543): Show |
chr15 | 66381912 | 66496544 |
| a0001c0001t0003 | 0/1 | 2547 | 51 | 3 | 13 | 17 | 7 | 10 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2542): Show |
chr15 | 66381912 | 66496544 |
| a0001c0001t0004 | 0/0 | 2547 | 19 | 1 | 0 | 17 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2542): Show |
chr15 | 66381912 | 66496544 |
| a0001c0001t0005 | 0/0 | 2547 | 10 | 0 | 2 | 5 | 1 | 2 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2542): Show |
chr15 | 66381912 | 66496544 |
| a0001c0001t0006 | 0/0 | 2547 | 7 | 0 | 2 | 0 | 3 | 2 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2542): Show |
chr15 | 66381912 | 66496544 |
| a0001c0001t0007 | 0/0 | 2548 | 2 | 1 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2543): Show |
chr15 | 66381912 | 66496544 |
| a0001c0001t0008 | 0/0 | 2548 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2543): Show |
chr15 | 66381912 | 66496544 |
| a0001c0001t0009 | 0/0 | 2548 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2543): Show |
chr15 | 66381912 | 66496544 |
| a0001c0001t0010 | 0/0 | 2547 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2542): Show |
chr15 | 66381912 | 66496544 |
| a0001c0001t0011 | 0/0 | 2547 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2542): Show |
chr15 | 66381912 | 66496544 |
| a0001c0001t0012 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2542): Show |
chr15 | 66381912 | 66496544 |
| a0001c0001t0013 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2542): Show |
chr15 | 66381912 | 66496544 |
| a0001c0001t0014 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2542): Show |
chr15 | 66381912 | 66496544 |
| a0001c0002t0001 | 0/0 | 2547 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2542): Show |
chr15 | 66381912 | 66496544 |
| a0001c0003t0001 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2542): Show |
chr15 | 66381912 | 66496544 |
| a0001c0004t0001 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2542): Show |
chr15 | 66381912 | 66496544 |
| a0001c0005t0002 | 0/0 | 2548 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2543): Show |
chr15 | 66381912 | 66496544 |
| a0001c0006t0001 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | AGTCC others(2542): Show |
chr15 | 66381912 | 66496544 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0006g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0006g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0009g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0010g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0011g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0012g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0013g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0014g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0005t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0006t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0195 | EUR | GBR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0061 | EUR | GBR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0192 | EUR | GBR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0070 | EUR | GBR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0157 | EUR | FIN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0007 | EUR | FIN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0191 | EUR | FIN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0371 | EUR | FIN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0243 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00673 | hp2 | a0001 | c0005 | t0002 | g0087 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0348 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0160 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0370 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0161 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0362 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0057 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0211 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0009 | EUR | IBS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0163 | EUR | IBS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0170 | EUR | IBS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | IBS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | IBS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0008 | EUR | IBS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0003 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02040 | hp2 | a0001 | c0001 | t0011 | g0269 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0361 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02145 | hp2 | a0001 | c0001 | t0012 | g0006 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | CDX | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CDX | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CDX | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CDX | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0351 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02572 | hp2 | a0001 | c0001 | t0014 | g0212 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0004 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0186 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0155 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0340 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0056 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0159 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0073 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0366 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0166 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0368 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03209 | hp2 | a0001 | c0006 | t0001 | g0353 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0179 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0360 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0158 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0005 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03704 | hp2 | a0001 | c0001 | t0010 | g0190 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0244 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0041 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0210 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0194 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0178 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0184 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | YRI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | CHB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0199 | AFR | YRI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0367 | AFR | YRI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18963 | hp2 | a0001 | c0001 | t0005 | g0239 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | LWK | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0365 | AFR | LWK | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | LWK | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | LWK | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0241 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19091 | hp1 | a0001 | c0001 | t0009 | g0165 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | YRI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | YRI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | ASW | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | ASW | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0055 | EUR | TSI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0173 | EUR | TSI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0369 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | USA | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | USA | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | USA | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | LWK | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | LWK | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0162 | REF | REF | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0105 | REF | REF | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:66387410 | C | T | 1 | a0001c0006 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.63C>T | p.Asn21Asn | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | 499/2547 | 63/1182 | 21/393 | chr15 | 66387410 | |||
| chr15:66481810 | C | T | 1 | a0001c0005 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.624C>T | p.Asp208Asp | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/11 | 1060/2547 | 624/1182 | 208/393 | chr15 | 66481810 | |||
| chr15:66487259 | A | T | 1 | a0001c0004 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.927A>T | p.Ala309Ala | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/11 | 1363/2547 | 927/1182 | 309/393 | chr15 | 66487259 | |||
| chr15:66490531 | T | C | 1 | a0001c0002 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.1098T>C | p.Ala366Ala | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 11/11 | 1534/2547 | 1098/1182 | 366/393 | chr15 | 66490531 | |||
| chr15:66490570 | C | T | 1 | a0001c0003 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1137C>T | p.Ile379Ile | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 11/11 | 1573/2547 | 1137/1182 | 379/393 | chr15 | 66490570 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:66386940 | G | T | 1 | a0001c0001t0014 | 1 | HG02572.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-408G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | chr15 | 66386940 | |||||||
| chr15:66387148 | G | A | 1 | a0001c0001t0008 | 1 | HG02886.hp1 | 5_prime_UTR_variant | MODIFIER | c.-200G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | 200 | chr15 | 66387148 | ||||||
| chr15:66387179 | A | G | 1 | a0001c0001t0013 | 1 | HG02280.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-169A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | chr15 | 66387179 | |||||||
| chr15:66387217 | C | T | 1 | a0001c0001t0012 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-131C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | 131 | chr15 | 66387217 | ||||||
| chr15:66387263 | G | C | 3 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0010 |
52 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(49): Show |
5_prime_UTR_variant | MODIFIER | c.-85G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | 85 | chr15 | 66387263 | ||||||
| chr15:66387311 | T | TC | 5 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(2): Show |
63 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(60): Show |
5_prime_UTR_variant | MODIFIER | c.-31dupC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | 30 | INFO_REALIGN_3_PRIME | chr15 | 66387311 | |||||
| chr15:66387346 | A | G | 1 | a0001c0001t0004 | 19 | HG00423.hp1 HG03927.hp2 NA18941.hp1 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-2A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | 2 | chr15 | 66387346 | ||||||
| chr15:66490923 | C | A | 3 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*308C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 11/11 | 308 | chr15 | 66490923 | ||||||
| chr15:66491272 | G | A | 2 | a0001c0001t0006 a0001c0001t0012 |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*657G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 11/11 | 657 | chr15 | 66491272 | ||||||
| chr15:66491375 | G | A | 1 | a0001c0001t0011 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 11/11 | 760 | chr15 | 66491375 | ||||||
| chr15:66491431 | A | C | 1 | a0001c0001t0007 | 2 | HG01255.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*816A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 11/11 | 816 | chr15 | 66491431 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:66387455 | G | C | 1 | a0001c0001t0001g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.80+28G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66387455 | |||||||
| chr15:66387460 | C | G | 2 | a0001c0001t0003g0370 a0001c0001t0003g0371 |
2 | HG00323.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.80+33C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66387460 | |||||||
| chr15:66387481 | G | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+54G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66387481 | |||||||
| chr15:66387512 | TG | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+87delG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66387512 | ||||||
| chr15:66387619 | TC | T | 29 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(26): Show |
29 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.80+195delC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66387619 | ||||||
| chr15:66387814 | G | C | 1 | a0001c0001t0001g0011 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.80+387G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66387814 | |||||||
| chr15:66387937 | G | A | 1 | a0001c0001t0002g0012 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.80+510G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66387937 | |||||||
| chr15:66387967 | C | T | 1 | a0001c0001t0002g0340 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.80+540C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66387967 | |||||||
| chr15:66388052 | C | G | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.80+625C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388052 | |||||||
| chr15:66388181 | C | G | 1 | a0001c0001t0001g0337 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.80+754C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388181 | |||||||
| chr15:66388213 | CG | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+787delG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388213 | |||||||
| chr15:66388214 | G | C | 1 | a0001c0001t0001g0272 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.80+787G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388214 | |||||||
| chr15:66388248 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.80+821T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388248 | |||||||
| chr15:66388307 | A | G | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80+880A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388307 | |||||||
| chr15:66388402 | C | T | 3 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 |
3 | HG01099.hp2 HG02004.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.80+975C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388402 | |||||||
| chr15:66388422 | C | T | 40 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(37): Show |
40 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.80+995C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388422 | |||||||
| chr15:66388596 | C | G | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.80+1169C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388596 | |||||||
| chr15:66388689 | A | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(77): Show |
81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.80+1262A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388689 | |||||||
| chr15:66388747 | C | T | 1 | a0001c0001t0001g0369 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.80+1320C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388747 | |||||||
| chr15:66388793 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | NA18946.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.80+1366C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388793 | |||||||
| chr15:66388904 | C | CT | 72 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(69): Show |
72 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.80+1496dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66388904 | ||||||
| chr15:66388904 | C | CTT | 79 | a0001c0001t0001g0011 a0001c0001t0001g0213 a0001c0001t0001g0214 others(76): Show |
79 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.80+1495_80+1496dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66388904 | ||||||
| chr15:66388904 | CT | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(75): Show |
79 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.80+1496delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66388904 | ||||||
| chr15:66389064 | G | T | 62 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(59): Show |
62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.80+1637G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389064 | |||||||
| chr15:66389114 | C | T | 1 | a0001c0001t0001g0317 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.80+1687C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389114 | |||||||
| chr15:66389176 | G | A | 10 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0159 others(7): Show |
10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.80+1749G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389176 | |||||||
| chr15:66389191 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80+1764C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389191 | |||||||
| chr15:66389307 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80+1880G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389307 | |||||||
| chr15:66389354 | T | C | 1 | a0001c0004t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80+1927T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389354 | |||||||
| chr15:66389440 | A | T | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.80+2013A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389440 | |||||||
| chr15:66389571 | GGTT | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+2145_80+2147del others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389571 | |||||||
| chr15:66389572 | G | GT | 38 | a0001c0001t0001g0046 a0001c0001t0001g0154 a0001c0001t0001g0247 others(35): Show |
38 | HG00423.hp2 HG00609.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.80+2169dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66389572 | ||||||
| chr15:66389572 | G | GTT | 33 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0143 others(30): Show |
33 | HG00438.hp1 HG00544.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.80+2168_80+2169dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66389572 | ||||||
| chr15:66389572 | G | GTTT | 29 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0121 others(26): Show |
29 | HG00609.hp2 HG01257.hp1 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.80+2167_80+2169dup others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66389572 | ||||||
| chr15:66389572 | G | GTTTT | 6 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0122 others(3): Show |
6 | HG00733.hp1 HG01934.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+2166_80+2169dup others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66389572 | ||||||
| chr15:66389572 | GT | G | 161 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(158): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.80+2169delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66389572 | ||||||
| chr15:66389573 | T | G | 6 | a0001c0001t0004g0020 a0001c0001t0004g0023 a0001c0001t0004g0028 others(3): Show |
6 | HG03927.hp2 NA18977.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.80+2146T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389573 | |||||||
| chr15:66389574 | T | G | 31 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(28): Show |
31 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.80+2147T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389574 | |||||||
| chr15:66389647 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.80+2220T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389647 | |||||||
| chr15:66389667 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(109): Show |
113 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.80+2240C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389667 | |||||||
| chr15:66389669 | G | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80+2242G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389669 | |||||||
| chr15:66389832 | A | G | 1 | a0001c0001t0001g0339 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.80+2405A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389832 | |||||||
| chr15:66390121 | A | G | 4 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
4 | HG02970.hp2 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+2694A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390121 | |||||||
| chr15:66390234 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+2807C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390234 | |||||||
| chr15:66390237 | G | C | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.80+2810G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390237 | |||||||
| chr15:66390271 | C | T | 1 | a0001c0001t0001g0338 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.80+2844C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390271 | |||||||
| chr15:66390371 | A | G | 31 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0213 others(28): Show |
31 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.80+2944A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390371 | |||||||
| chr15:66390603 | A | G | 1 | a0001c0001t0014g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80+3176A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390603 | |||||||
| chr15:66390613 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+3186T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390613 | |||||||
| chr15:66390883 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+3456C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390883 | |||||||
| chr15:66391057 | CT | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(264): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.80+3646delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66391057 | ||||||
| chr15:66391057 | CTT | C | 44 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(41): Show |
44 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.80+3645_80+3646del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66391057 | ||||||
| chr15:66391066 | T | C | 1 | a0001c0001t0003g0163 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.80+3639T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391066 | |||||||
| chr15:66391123 | C | T | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.80+3696C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391123 | |||||||
| chr15:66391134 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.80+3707C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391134 | |||||||
| chr15:66391267 | C | G | 1 | a0001c0001t0001g0339 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.80+3840C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391267 | |||||||
| chr15:66391319 | C | T | 1 | a0001c0001t0002g0100 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.80+3892C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391319 | |||||||
| chr15:66391357 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.80+3930C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391357 | |||||||
| chr15:66391382 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.80+3955A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391382 | |||||||
| chr15:66391655 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+4228G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391655 | |||||||
| chr15:66391777 | C | T | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.80+4350C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391777 | |||||||
| chr15:66392052 | C | T | 89 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0213 others(86): Show |
89 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.80+4625C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392052 | |||||||
| chr15:66392207 | A | G | 6 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG02486.hp2 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.80+4780A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392207 | |||||||
| chr15:66392248 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.80+4821T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392248 | |||||||
| chr15:66392253 | G | T | 1 | a0001c0001t0001g0307 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.80+4826G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392253 | |||||||
| chr15:66392254 | G | GTT | 6 | a0001c0001t0001g0156 a0001c0001t0001g0248 a0001c0001t0001g0249 others(3): Show |
6 | HG02273.hp1 HG02622.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | |||||||
| chr15:66392254 | G | GTTT | 46 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
47 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | |||||||
| chr15:66392254 | G | GTTTT | 84 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0118 others(81): Show |
84 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | |||||||
| chr15:66392254 | G | GTTTTT | 76 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0298 others(73): Show |
76 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(73): Show |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | |||||||
| chr15:66392254 | G | GTTTTTT | 20 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(17): Show |
20 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | |||||||
| chr15:66392254 | G | GTTTTTTT | 15 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0222 others(12): Show |
15 | HG00642.hp2 HG01071.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(7): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | |||||||
| chr15:66392254 | G | GTTTTTTT others(1): Show |
6 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(3): Show |
6 | HG01069.hp2 HG02165.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | |||||||
| chr15:66392254 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0002g0113 a0001c0001t0002g0340 |
2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | |||||||
| chr15:66392254 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0002g0114 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.80+4827_80+4828ins others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | |||||||
| chr15:66392254 | GGTTTTTT others(1): Show |
G | 12 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(9): Show |
12 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.80+4828_80+4835del others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | |||||||
| chr15:66392255 | G | GTTTTTTT others(4): Show |
2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.80+4842_80+4852dup others(11): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392255 | ||||||
| chr15:66392255 | G | GTTTTTTT others(5): Show |
3 | a0001c0001t0001g0325 a0001c0001t0001g0347 a0001c0001t0001g0348 |
3 | HG00733.hp2 HG01069.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.80+4841_80+4852dup others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392255 | ||||||
| chr15:66392255 | G | GTTTTTTT others(6): Show |
11 | a0001c0001t0001g0011 a0001c0001t0001g0326 a0001c0001t0001g0327 others(8): Show |
11 | HG02280.hp2 HG02896.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.80+4840_80+4852dup others(13): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392255 | ||||||
| chr15:66392255 | G | GTTTTTTT others(7): Show |
9 | a0001c0001t0001g0328 a0001c0001t0001g0329 a0001c0001t0001g0356 others(6): Show |
9 | HG01109.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.80+4839_80+4852dup others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392255 | ||||||
| chr15:66392255 | G | GTTTTTTT others(8): Show |
4 | a0001c0001t0001g0330 a0001c0001t0001g0363 a0001c0001t0001g0364 others(1): Show |
4 | HG01891.hp2 HG02886.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+4838_80+4852dup others(15): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392255 | ||||||
| chr15:66392255 | G | GTTTTTTT others(17): Show |
1 | a0001c0001t0001g0366 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.80+4829_80+4852dup others(24): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392255 | ||||||
| chr15:66392255 | G | GTTTTTTT others(18): Show |
2 | a0001c0001t0001g0367 a0001c0001t0001g0369 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.80+4852_80+4853ins others(25): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392255 | ||||||
| chr15:66392255 | G | T | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(300): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.80+4828G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392255 | |||||||
| chr15:66392279 | T | TTA | 33 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(30): Show |
33 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.80+4852_80+4853ins others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392279 | |||||||
| chr15:66392279 | T | TTTA | 7 | a0001c0001t0001g0045 a0001c0001t0001g0335 a0001c0001t0004g0041 others(4): Show |
7 | HG01243.hp2 HG02004.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.80+4852_80+4853ins others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392279 | |||||||
| chr15:66392293 | G | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80+4866G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392293 | |||||||
| chr15:66392335 | C | T | 15 | a0001c0001t0001g0221 a0001c0001t0001g0229 a0001c0001t0001g0230 others(12): Show |
15 | HG00280.hp2 HG00639.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.80+4908C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392335 | |||||||
| chr15:66392408 | G | C | 2 | a0001c0001t0001g0218 a0001c0001t0001g0232 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.80+4981G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392408 | |||||||
| chr15:66392434 | T | C | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(359): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.80+5007T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392434 | |||||||
| chr15:66392524 | A | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.80+5097A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392524 | |||||||
| chr15:66392554 | C | CT | 50 | a0001c0001t0001g0011 a0001c0001t0001g0279 a0001c0001t0001g0295 others(47): Show |
50 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.80+5143dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392554 | ||||||
| chr15:66392554 | CT | C | 23 | a0001c0001t0001g0222 a0001c0001t0001g0251 a0001c0001t0002g0048 others(20): Show |
23 | HG00423.hp1 HG01256.hp1 HG03491.hp1 others(20): Show |
intron_variant | MODIFIER | c.80+5143delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392554 | ||||||
| chr15:66392600 | C | T | 38 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(35): Show |
38 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.80+5173C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392600 | |||||||
| chr15:66392639 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80+5212C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392639 | |||||||
| chr15:66392697 | G | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG00738.hp2 HG01106.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.80+5270G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392697 | |||||||
| chr15:66392897 | A | G | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.80+5470A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392897 | |||||||
| chr15:66392957 | C | T | 37 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(34): Show |
37 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.80+5530C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392957 | |||||||
| chr15:66393182 | C | CT | 12 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0156 others(9): Show |
12 | HG00280.hp2 HG00639.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.80+5768dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66393182 | ||||||
| chr15:66393309 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.80+5882C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66393309 | |||||||
| chr15:66393470 | C | T | 28 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0213 others(25): Show |
28 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.80+6043C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66393470 | |||||||
| chr15:66393581 | T | C | 2 | a0001c0001t0001g0229 a0001c0001t0001g0237 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.80+6154T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66393581 | |||||||
| chr15:66393634 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+6207A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66393634 | |||||||
| chr15:66393896 | G | T | 1 | a0001c0001t0006g0010 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.80+6469G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66393896 | |||||||
| chr15:66393896 | GT | G | 5 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0340 others(2): Show |
5 | HG01255.hp2 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+6470delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66393896 | |||||||
| chr15:66394229 | G | A | 1 | a0001c0001t0006g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.80+6802G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394229 | |||||||
| chr15:66394389 | A | G | 2 | a0001c0001t0002g0088 a0001c0005t0002g0087 |
2 | HG00673.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.80+6962A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394389 | |||||||
| chr15:66394390 | C | CAGGTTGA others(34): Show |
8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+6964_80+7004dup others(41): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66394390 | ||||||
| chr15:66394432 | G | A | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.80+7005G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394432 | |||||||
| chr15:66394454 | A | C | 1 | a0001c0004t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80+7027A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394454 | |||||||
| chr15:66394459 | C | CT | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0309 others(4): Show |
7 | HG00642.hp1 HG01168.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.80+7053dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66394459 | ||||||
| chr15:66394459 | C | CTT | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+7052_80+7053dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66394459 | ||||||
| chr15:66394459 | CT | C | 13 | a0001c0001t0001g0101 a0001c0001t0001g0118 a0001c0001t0001g0143 others(10): Show |
13 | HG00621.hp1 HG00642.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.80+7053delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66394459 | ||||||
| chr15:66394491 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+7064G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394491 | |||||||
| chr15:66394648 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+7221G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394648 | |||||||
| chr15:66394690 | A | G | 2 | a0001c0001t0001g0347 a0001c0001t0001g0348 |
2 | HG00733.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.80+7263A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394690 | |||||||
| chr15:66394745 | T | A | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.80+7318T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394745 | |||||||
| chr15:66394840 | A | G | 5 | a0001c0001t0002g0055 a0001c0001t0002g0086 a0001c0001t0002g0095 others(2): Show |
5 | HG00597.hp2 NA18962.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+7413A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394840 | |||||||
| chr15:66394919 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+7492C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394919 | |||||||
| chr15:66394989 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80+7562A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394989 | |||||||
| chr15:66395229 | T | C | 1 | a0001c0001t0001g0338 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.80+7802T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395229 | |||||||
| chr15:66395484 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.80+8057A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395484 | |||||||
| chr15:66395573 | A | ATTTT | 7 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0007 others(4): Show |
7 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.80+8162_80+8165dup others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66395573 | ||||||
| chr15:66395573 | AT | A | 50 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0101 others(47): Show |
50 | HG00733.hp2 HG00735.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.80+8165delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66395573 | ||||||
| chr15:66395573 | ATT | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(291): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.80+8164_80+8165del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66395573 | ||||||
| chr15:66395573 | ATTT | A | 6 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+8163_80+8165del others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66395573 | ||||||
| chr15:66395686 | C | T | 37 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(34): Show |
37 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.80+8259C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395686 | |||||||
| chr15:66395696 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.80+8269C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395696 | |||||||
| chr15:66395736 | C | T | 4 | a0001c0001t0004g0028 a0001c0001t0004g0029 a0001c0001t0004g0043 others(1): Show |
4 | NA19006.hp1 NA19009.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.80+8309C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395736 | |||||||
| chr15:66395753 | T | C | 1 | a0001c0001t0002g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.80+8326T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395753 | |||||||
| chr15:66395766 | C | G | 1 | a0001c0001t0001g0327 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.80+8339C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395766 | |||||||
| chr15:66395812 | A | G | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(2): Show |
5 | HG01255.hp1 HG01261.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.80+8385A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395812 | |||||||
| chr15:66395857 | G | A | 4 | a0001c0001t0001g0295 a0001c0001t0002g0113 a0001c0001t0002g0114 others(1): Show |
4 | HG00735.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.80+8430G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395857 | |||||||
| chr15:66396091 | A | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0003g0164 |
3 | HG03453.hp2 HG03491.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.80+8664A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396091 | |||||||
| chr15:66396133 | A | G | 3 | a0001c0001t0006g0005 a0001c0001t0006g0008 a0001c0001t0006g0009 |
3 | HG01515.hp1 HG01517.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.80+8706A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396133 | |||||||
| chr15:66396273 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.80+8846G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396273 | |||||||
| chr15:66396315 | C | G | 359 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(356): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.80+8888C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396315 | |||||||
| chr15:66396415 | A | C | 2 | a0001c0001t0001g0304 a0001c0001t0001g0306 |
2 | HG01952.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.80+8988A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396415 | |||||||
| chr15:66396428 | G | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+9001G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396428 | |||||||
| chr15:66396443 | T | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.80+9016T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396443 | |||||||
| chr15:66396469 | C | T | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.80+9042C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396469 | |||||||
| chr15:66396617 | G | A | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.80+9190G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396617 | |||||||
| chr15:66396660 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.80+9233A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396660 | |||||||
| chr15:66396878 | T | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0326 a0001c0001t0001g0328 others(1): Show |
4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+9451T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396878 | |||||||
| chr15:66396888 | T | C | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.80+9461T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396888 | |||||||
| chr15:66396930 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(50): Show |
54 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.80+9503C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396930 | |||||||
| chr15:66396952 | T | G | 1 | a0001c0001t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.80+9525T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396952 | |||||||
| chr15:66396964 | C | T | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.80+9537C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396964 | |||||||
| chr15:66396967 | G | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.80+9540G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396967 | |||||||
| chr15:66396968 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0142 |
2 | NA18968.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.80+9541A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396968 | |||||||
| chr15:66396995 | C | CT | 15 | a0001c0001t0001g0037 a0001c0001t0001g0101 a0001c0001t0001g0107 others(12): Show |
15 | HG01433.hp1 HG02027.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.80+9595dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66396995 | ||||||
| chr15:66396995 | CT | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(177): Show |
181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.80+9595delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66396995 | ||||||
| chr15:66396995 | CTT | C | 46 | a0001c0001t0001g0011 a0001c0001t0001g0249 a0001c0001t0001g0325 others(43): Show |
46 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.80+9594_80+9595del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66396995 | ||||||
| chr15:66396995 | CTTTTTT | C | 57 | a0001c0001t0002g0012 a0001c0001t0002g0049 a0001c0001t0002g0050 others(54): Show |
57 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.80+9590_80+9595del others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66396995 | ||||||
| chr15:66396995 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80+9584_80+9595del others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66396995 | ||||||
| chr15:66397076 | C | T | 1 | a0001c0001t0014g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80+9649C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397076 | |||||||
| chr15:66397133 | T | C | 1 | a0001c0001t0001g0309 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.80+9706T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397133 | |||||||
| chr15:66397145 | C | T | 3 | a0001c0001t0001g0248 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.80+9718C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397145 | |||||||
| chr15:66397196 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+9769A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397196 | |||||||
| chr15:66397291 | C | T | 1 | a0001c0001t0003g0210 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80+9864C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397291 | |||||||
| chr15:66397294 | C | T | 2 | a0001c0001t0005g0160 a0001c0001t0005g0161 |
2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.80+9867C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397294 | |||||||
| chr15:66397442 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80+10015C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397442 | |||||||
| chr15:66397462 | A | C | 2 | a0001c0001t0003g0183 a0001c0001t0003g0187 |
2 | NA18747.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.80+10035A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397462 | |||||||
| chr15:66397535 | C | T | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80+10108C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397535 | |||||||
| chr15:66397536 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+10109G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397536 | |||||||
| chr15:66397684 | T | G | 1 | a0001c0001t0001g0333 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.80+10257T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397684 | |||||||
| chr15:66397773 | T | G | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.80+10346T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397773 | |||||||
| chr15:66397797 | C | T | 2 | a0001c0001t0001g0358 a0001c0001t0001g0359 |
2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.80+10370C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397797 | |||||||
| chr15:66397846 | G | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.80+10419G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397846 | |||||||
| chr15:66397862 | G | A | 31 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0213 others(28): Show |
31 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.80+10435G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397862 | |||||||
| chr15:66397931 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.80+10504A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397931 | |||||||
| chr15:66397972 | C | G | 1 | a0001c0001t0001g0302 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.80+10545C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397972 | |||||||
| chr15:66398100 | T | TA | 6 | a0001c0001t0001g0307 a0001c0001t0002g0060 a0001c0001t0002g0084 others(3): Show |
6 | HG02056.hp2 NA18940.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+10685dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66398100 | ||||||
| chr15:66398110 | A | G | 31 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0213 others(28): Show |
31 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.80+10683A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398110 | |||||||
| chr15:66398145 | C | G | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.80+10718C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398145 | |||||||
| chr15:66398152 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+10725C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398152 | |||||||
| chr15:66398173 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.80+10746G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398173 | |||||||
| chr15:66398178 | C | A | 1 | a0001c0001t0001g0238 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.80+10751C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398178 | |||||||
| chr15:66398255 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.80+10828A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398255 | |||||||
| chr15:66398291 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.80+10864G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398291 | |||||||
| chr15:66398369 | C | T | 1 | a0001c0001t0014g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80+10942C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398369 | |||||||
| chr15:66398386 | G | T | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80+10959G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398386 | |||||||
| chr15:66398438 | A | G | 58 | a0001c0001t0002g0012 a0001c0001t0002g0049 a0001c0001t0002g0050 others(55): Show |
58 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.80+11011A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398438 | |||||||
| chr15:66398447 | A | G | 1 | a0001c0001t0006g0005 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.80+11020A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398447 | |||||||
| chr15:66398453 | G | T | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.80+11026G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398453 | |||||||
| chr15:66398454 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.80+11027C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398454 | |||||||
| chr15:66398490 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.80+11063C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398490 | |||||||
| chr15:66398514 | T | C | 359 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(356): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.80+11087T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398514 | |||||||
| chr15:66398568 | T | C | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(359): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.80+11141T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398568 | |||||||
| chr15:66398693 | TTG | T | 3 | a0001c0001t0001g0248 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.80+11270_80+11271d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66398693 | ||||||
| chr15:66398768 | A | AT | 10 | a0001c0001t0003g0208 a0001c0001t0005g0157 a0001c0001t0005g0158 others(7): Show |
10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.80+11353dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66398768 | ||||||
| chr15:66398779 | TTC | T | 26 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(23): Show |
26 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.80+11354_80+11355d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66398779 | ||||||
| chr15:66398781 | C | T | 51 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(48): Show |
51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.80+11354C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398781 | |||||||
| chr15:66398781 | CT | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(229): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.80+11365delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66398781 | ||||||
| chr15:66398782 | T | C | 77 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(74): Show |
77 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.80+11355T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398782 | |||||||
| chr15:66398837 | G | A | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | NA19065.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.80+11410G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398837 | |||||||
| chr15:66398939 | A | C | 1 | a0001c0001t0009g0165 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.80+11512A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398939 | |||||||
| chr15:66399136 | A | G | 4 | a0001c0001t0002g0083 a0001c0001t0002g0088 a0001c0001t0002g0150 others(1): Show |
4 | HG00673.hp2 HG02165.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+11709A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399136 | |||||||
| chr15:66399357 | A | C | 1 | a0001c0001t0003g0182 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.80+11930A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399357 | |||||||
| chr15:66399455 | CT | C | 37 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(34): Show |
37 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.80+12037delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66399455 | ||||||
| chr15:66399519 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.80+12092G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399519 | |||||||
| chr15:66399588 | G | A | 1 | a0001c0005t0002g0087 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.80+12161G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399588 | |||||||
| chr15:66399612 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+12185A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399612 | |||||||
| chr15:66399636 | G | A | 1 | a0001c0001t0014g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80+12209G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399636 | |||||||
| chr15:66399837 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(111): Show |
115 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.80+12410C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399837 | |||||||
| chr15:66399838 | G | T | 1 | a0001c0001t0014g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80+12411G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399838 | |||||||
| chr15:66399872 | G | A | 1 | a0001c0001t0001g0341 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80+12445G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399872 | |||||||
| chr15:66400036 | A | G | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.80+12609A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400036 | |||||||
| chr15:66400107 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+12680G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400107 | |||||||
| chr15:66400174 | A | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+12747A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400174 | |||||||
| chr15:66400183 | G | T | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.80+12756G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400183 | |||||||
| chr15:66400184 | C | T | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.80+12757C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400184 | |||||||
| chr15:66400238 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.80+12811G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400238 | |||||||
| chr15:66400283 | CA | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+12859delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66400283 | ||||||
| chr15:66400317 | C | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(79): Show |
83 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.80+12890C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400317 | |||||||
| chr15:66400396 | A | G | 1 | a0001c0001t0003g0181 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.80+12969A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400396 | |||||||
| chr15:66400441 | A | G | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.80+13014A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400441 | |||||||
| chr15:66400501 | A | G | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(359): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.80+13074A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400501 | |||||||
| chr15:66400506 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.80+13079C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400506 | |||||||
| chr15:66400540 | C | T | 4 | a0001c0001t0003g0163 a0001c0001t0003g0180 a0001c0001t0003g0182 others(1): Show |
4 | HG01106.hp2 HG01515.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+13113C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400540 | |||||||
| chr15:66400657 | A | G | 1 | a0001c0001t0001g0337 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.80+13230A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400657 | |||||||
| chr15:66400790 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(319): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.80+13363A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400790 | |||||||
| chr15:66400848 | C | T | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(359): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.80+13421C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400848 | |||||||
| chr15:66400904 | T | G | 1 | a0001c0001t0001g0214 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.80+13477T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400904 | |||||||
| chr15:66400940 | T | C | 3 | a0001c0001t0001g0342 a0001c0001t0001g0343 a0001c0001t0001g0344 |
3 | HG01884.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.80+13513T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400940 | |||||||
| chr15:66400976 | A | G | 31 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(28): Show |
31 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.80+13549A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400976 | |||||||
| chr15:66400977 | T | C | 1 | a0001c0001t0001g0339 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.80+13550T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400977 | |||||||
| chr15:66401017 | G | A | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(359): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.80+13590G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401017 | |||||||
| chr15:66401022 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+13595T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401022 | |||||||
| chr15:66401027 | T | C | 1 | a0001c0001t0001g0338 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.80+13600T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401027 | |||||||
| chr15:66401321 | T | A | 1 | a0001c0001t0001g0016 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.80+13894T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401321 | |||||||
| chr15:66401435 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+14008G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401435 | |||||||
| chr15:66401530 | G | C | 40 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(37): Show |
40 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.80+14103G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401530 | |||||||
| chr15:66401532 | A | C | 1 | a0001c0004t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80+14105A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401532 | |||||||
| chr15:66401543 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.80+14116G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401543 | |||||||
| chr15:66401792 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0001g0233 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.80+14365G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401792 | |||||||
| chr15:66402082 | A | T | 26 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(23): Show |
26 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.80+14655A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402082 | |||||||
| chr15:66402093 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(111): Show |
115 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.80+14666A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402093 | |||||||
| chr15:66402198 | C | T | 6 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG02486.hp2 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.80+14771C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402198 | |||||||
| chr15:66402220 | A | C | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.80+14793A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402220 | |||||||
| chr15:66402229 | G | A | 5 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+14802G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402229 | |||||||
| chr15:66402308 | T | C | 1 | a0001c0004t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80+14881T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402308 | |||||||
| chr15:66402360 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.80+14933G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402360 | |||||||
| chr15:66402536 | G | A | 1 | a0001c0001t0001g0339 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.80+15109G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402536 | |||||||
| chr15:66402636 | C | T | 1 | a0001c0001t0014g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80+15209C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402636 | |||||||
| chr15:66402696 | A | G | 40 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(37): Show |
40 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.80+15269A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402696 | |||||||
| chr15:66402889 | G | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+15462G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402889 | |||||||
| chr15:66402922 | G | T | 2 | a0001c0001t0006g0008 a0001c0001t0006g0009 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.80+15495G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402922 | |||||||
| chr15:66403154 | C | G | 1 | a0001c0001t0001g0344 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.80+15727C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403154 | |||||||
| chr15:66403296 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.80+15869T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403296 | |||||||
| chr15:66403301 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.80+15874A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403301 | |||||||
| chr15:66403358 | G | C | 1 | a0001c0001t0001g0338 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.80+15931G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403358 | |||||||
| chr15:66403705 | C | T | 1 | a0001c0001t0003g0204 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.80+16278C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403705 | |||||||
| chr15:66403713 | T | C | 3 | a0001c0001t0002g0059 a0001c0001t0002g0062 a0001c0001t0002g0110 |
3 | HG02148.hp2 HG02273.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.80+16286T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403713 | |||||||
| chr15:66403716 | A | G | 2 | a0001c0001t0001g0347 a0001c0001t0001g0348 |
2 | HG00733.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.80+16289A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403716 | |||||||
| chr15:66403725 | C | T | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.80+16298C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403725 | |||||||
| chr15:66403743 | A | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.80+16316A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403743 | |||||||
| chr15:66403829 | C | G | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80+16402C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403829 | |||||||
| chr15:66403854 | T | C | 3 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0065 |
3 | NA18946.hp2 NA19056.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.80+16427T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403854 | |||||||
| chr15:66403994 | T | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+16567T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403994 | |||||||
| chr15:66403999 | C | G | 1 | a0001c0001t0001g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.80+16572C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403999 | |||||||
| chr15:66404003 | A | G | 3 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0340 |
3 | HG02109.hp1 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.80+16576A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404003 | |||||||
| chr15:66404021 | GCTC | G | 3 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 |
3 | HG01099.hp2 HG02004.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.80+16598_80+16600d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66404021 | ||||||
| chr15:66404245 | C | T | 1 | a0001c0001t0003g0204 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.80+16818C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404245 | |||||||
| chr15:66404397 | A | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(160): Show |
164 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.80+16970A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404397 | |||||||
| chr15:66404604 | A | G | 1 | a0001c0001t0002g0100 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.80+17177A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404604 | |||||||
| chr15:66404720 | G | A | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(315): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.80+17293G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404720 | |||||||
| chr15:66404775 | G | A | 2 | a0001c0001t0005g0160 a0001c0001t0005g0161 |
2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.80+17348G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404775 | |||||||
| chr15:66404813 | A | C | 1 | a0001c0001t0003g0211 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.80+17386A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404813 | |||||||
| chr15:66404889 | T | C | 359 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(356): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.80+17462T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404889 | |||||||
| chr15:66404945 | G | A | 1 | a0001c0001t0003g0191 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.80+17518G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404945 | |||||||
| chr15:66405060 | T | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG00438.hp1 HG02155.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.80+17633T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405060 | |||||||
| chr15:66405405 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+17978T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405405 | |||||||
| chr15:66405499 | T | A | 1 | a0001c0001t0001g0285 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.80+18072T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405499 | |||||||
| chr15:66405539 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.80+18112A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405539 | |||||||
| chr15:66405603 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.80+18176G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405603 | |||||||
| chr15:66405721 | C | A | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.80+18294C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405721 | |||||||
| chr15:66405782 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0142 |
2 | NA18968.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.80+18355G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405782 | |||||||
| chr15:66405794 | T | C | 1 | a0001c0001t0004g0017 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.80+18367T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405794 | |||||||
| chr15:66405834 | G | A | 40 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(37): Show |
40 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.80+18407G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405834 | |||||||
| chr15:66406001 | T | C | 1 | a0001c0001t0001g0305 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.80+18574T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66406001 | |||||||
| chr15:66406242 | T | C | 40 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(37): Show |
40 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.80+18815T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66406242 | |||||||
| chr15:66406375 | A | G | 1 | a0001c0001t0002g0054 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.80+18948A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66406375 | |||||||
| chr15:66406575 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.80+19148A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66406575 | |||||||
| chr15:66406805 | C | T | 6 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(3): Show |
6 | HG00558.hp1 HG00673.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+19378C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66406805 | |||||||
| chr15:66406884 | T | G | 1 | a0001c0001t0002g0066 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.80+19457T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66406884 | |||||||
| chr15:66406905 | G | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.80+19478G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66406905 | |||||||
| chr15:66407016 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.80+19589A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407016 | |||||||
| chr15:66407020 | A | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0232 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.80+19593A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407020 | |||||||
| chr15:66407107 | C | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01261.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+19680C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407107 | |||||||
| chr15:66407380 | C | T | 38 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(35): Show |
38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.80+19953C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407380 | |||||||
| chr15:66407390 | T | C | 38 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(35): Show |
38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.80+19963T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407390 | |||||||
| chr15:66407416 | A | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0318 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.80+19989A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407416 | |||||||
| chr15:66407605 | C | A | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(359): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.80+20178C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407605 | |||||||
| chr15:66407629 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80+20202G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407629 | |||||||
| chr15:66407957 | C | T | 2 | a0001c0001t0003g0178 a0001c0001t0003g0179 |
2 | HG03490.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.80+20530C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407957 | |||||||
| chr15:66408219 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.80+20792G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66408219 | |||||||
| chr15:66408238 | T | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.80+20811T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66408238 | |||||||
| chr15:66408341 | AG | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80+20916delG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66408341 | ||||||
| chr15:66408419 | C | T | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.80+20992C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66408419 | |||||||
| chr15:66408859 | T | C | 364 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(361): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.80+21432T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66408859 | |||||||
| chr15:66409162 | G | A | 62 | a0001c0001t0001g0363 a0001c0001t0003g0163 a0001c0001t0003g0164 others(59): Show |
62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.80+21735G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66409162 | |||||||
| chr15:66409490 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.80+22063G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66409490 | |||||||
| chr15:66409766 | A | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+22339A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66409766 | |||||||
| chr15:66409862 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.80+22435A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66409862 | |||||||
| chr15:66409928 | C | T | 37 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(34): Show |
37 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.80+22501C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66409928 | |||||||
| chr15:66409974 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.80+22547A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66409974 | |||||||
| chr15:66409981 | C | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+22554C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66409981 | |||||||
| chr15:66410007 | C | A | 51 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(48): Show |
51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.80+22580C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410007 | |||||||
| chr15:66410122 | C | A | 3 | a0001c0001t0002g0086 a0001c0001t0002g0095 a0001c0001t0002g0096 |
3 | NA18962.hp2 NA19002.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.80+22695C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410122 | |||||||
| chr15:66410185 | C | A | 61 | a0001c0001t0002g0012 a0001c0001t0002g0049 a0001c0001t0002g0050 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.80+22758C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410185 | |||||||
| chr15:66410208 | T | C | 61 | a0001c0001t0002g0012 a0001c0001t0002g0049 a0001c0001t0002g0050 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.80+22781T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410208 | |||||||
| chr15:66410423 | AAGAG | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+23000_80+23003d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66410423 | ||||||
| chr15:66410586 | T | C | 1 | a0001c0001t0012g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.80+23159T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410586 | |||||||
| chr15:66410604 | T | A | 1 | a0001c0001t0002g0067 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.80+23177T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410604 | |||||||
| chr15:66410620 | GA | G | 26 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(23): Show |
26 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.80+23199delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66410620 | ||||||
| chr15:66410770 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.80+23343G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410770 | |||||||
| chr15:66410873 | C | G | 40 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(37): Show |
40 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.80+23446C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410873 | |||||||
| chr15:66410989 | A | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80+23562A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410989 | |||||||
| chr15:66411041 | A | G | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.80+23614A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411041 | |||||||
| chr15:66411094 | T | G | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.80+23667T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411094 | |||||||
| chr15:66411138 | A | T | 61 | a0001c0001t0002g0012 a0001c0001t0002g0049 a0001c0001t0002g0050 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.80+23711A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411138 | |||||||
| chr15:66411173 | G | A | 6 | a0001c0001t0004g0018 a0001c0001t0004g0019 a0001c0001t0004g0020 others(3): Show |
6 | NA18941.hp1 NA18944.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+23746G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411173 | |||||||
| chr15:66411199 | G | C | 1 | a0001c0001t0001g0255 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.80+23772G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411199 | |||||||
| chr15:66411287 | G | T | 3 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0159 |
3 | HG00280.hp1 HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.81-23740G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411287 | |||||||
| chr15:66411288 | T | C | 3 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0159 |
3 | HG00280.hp1 HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.81-23739T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411288 | |||||||
| chr15:66411290 | G | T | 3 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0159 |
3 | HG00280.hp1 HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.81-23737G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411290 | |||||||
| chr15:66411291 | G | T | 3 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0159 |
3 | HG00280.hp1 HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.81-23736G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411291 | |||||||
| chr15:66411343 | CCT | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-23680_81-23679d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66411343 | ||||||
| chr15:66411352 | A | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | HG02970.hp2 HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.81-23675A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411352 | |||||||
| chr15:66411359 | A | G | 6 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG02486.hp2 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.81-23668A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411359 | |||||||
| chr15:66411421 | C | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-23606C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411421 | |||||||
| chr15:66411534 | T | G | 1 | a0001c0001t0001g0120 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.81-23493T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411534 | |||||||
| chr15:66411626 | A | G | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-23401A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411626 | |||||||
| chr15:66411686 | T | C | 3 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0065 |
3 | NA18946.hp2 NA19056.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.81-23341T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411686 | |||||||
| chr15:66411769 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0111 |
2 | HG02486.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.81-23258T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411769 | |||||||
| chr15:66411928 | T | G | 1 | a0001c0001t0002g0068 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.81-23099T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411928 | |||||||
| chr15:66412051 | A | G | 1 | a0001c0001t0002g0149 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.81-22976A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66412051 | |||||||
| chr15:66412111 | G | A | 38 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(35): Show |
38 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.81-22916G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66412111 | |||||||
| chr15:66412270 | C | T | 1 | a0001c0001t0003g0174 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.81-22757C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66412270 | |||||||
| chr15:66412668 | C | T | 1 | a0001c0001t0006g0003 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.81-22359C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66412668 | |||||||
| chr15:66412705 | G | A | 91 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(88): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.81-22322G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66412705 | |||||||
| chr15:66412837 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(80): Show |
84 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.81-22190C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66412837 | |||||||
| chr15:66412966 | G | A | 2 | a0001c0001t0001g0341 a0001c0001t0001g0345 |
2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.81-22061G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66412966 | |||||||
| chr15:66413053 | G | A | 3 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0340 |
3 | HG02109.hp1 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.81-21974G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413053 | |||||||
| chr15:66413096 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.81-21931A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413096 | |||||||
| chr15:66413123 | T | C | 1 | a0001c0001t0014g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.81-21904T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413123 | |||||||
| chr15:66413150 | C | T | 38 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(35): Show |
38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.81-21877C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413150 | |||||||
| chr15:66413191 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-21836T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413191 | |||||||
| chr15:66413239 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-21788A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413239 | |||||||
| chr15:66413249 | A | C | 1 | a0001c0001t0001g0325 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.81-21778A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413249 | |||||||
| chr15:66413278 | C | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-21749C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413278 | |||||||
| chr15:66413398 | G | C | 1 | a0001c0001t0003g0175 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.81-21629G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413398 | |||||||
| chr15:66413618 | G | A | 1 | a0001c0001t0003g0205 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.81-21409G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413618 | |||||||
| chr15:66413624 | AT | A | 351 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(348): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.81-21392delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66413624 | ||||||
| chr15:66413624 | ATT | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-21393_81-21392d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66413624 | ||||||
| chr15:66413673 | G | C | 1 | a0001c0001t0002g0068 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.81-21354G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413673 | |||||||
| chr15:66413698 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.81-21329T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413698 | |||||||
| chr15:66413786 | G | A | 2 | a0001c0001t0002g0069 a0001c0001t0002g0090 |
2 | NA18943.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.81-21241G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413786 | |||||||
| chr15:66413832 | T | C | 1 | a0001c0001t0001g0309 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.81-21195T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413832 | |||||||
| chr15:66413878 | C | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-21149C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413878 | |||||||
| chr15:66413886 | T | C | 62 | a0001c0001t0002g0012 a0001c0001t0002g0048 a0001c0001t0002g0049 others(59): Show |
62 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.81-21141T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413886 | |||||||
| chr15:66413911 | C | CT | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(292): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.81-21100dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66413911 | ||||||
| chr15:66413911 | C | CTT | 6 | a0001c0001t0001g0285 a0001c0001t0001g0301 a0001c0001t0002g0099 others(3): Show |
6 | HG00280.hp1 HG02735.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-21101_81-21100d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66413911 | ||||||
| chr15:66413911 | C | CTTT | 35 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(32): Show |
35 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.81-21102_81-21100d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66413911 | ||||||
| chr15:66413955 | C | CT | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-21060dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66413955 | ||||||
| chr15:66413967 | T | A | 2 | a0001c0001t0003g0182 a0001c0001t0003g0207 |
2 | HG01106.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.81-21060T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413967 | |||||||
| chr15:66414010 | C | A | 1 | a0001c0001t0002g0071 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.81-21017C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414010 | |||||||
| chr15:66414167 | G | A | 38 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(35): Show |
38 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.81-20860G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414167 | |||||||
| chr15:66414198 | GAGTCAGG others(140): Show |
G | 40 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(37): Show |
40 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.81-20825_81-20679d others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66414198 | ||||||
| chr15:66414366 | A | G | 46 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(43): Show |
46 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.81-20661A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414366 | |||||||
| chr15:66414407 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(80): Show |
84 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.81-20620A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414407 | |||||||
| chr15:66414539 | T | C | 2 | a0001c0001t0006g0008 a0001c0001t0006g0009 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.81-20488T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414539 | |||||||
| chr15:66414574 | C | T | 1 | a0001c0001t0002g0084 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.81-20453C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414574 | |||||||
| chr15:66414781 | C | CT | 40 | a0001c0001t0001g0011 a0001c0001t0001g0145 a0001c0001t0001g0325 others(37): Show |
40 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.81-20231dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66414781 | ||||||
| chr15:66414781 | CT | C | 6 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-20231delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66414781 | ||||||
| chr15:66414796 | T | C | 37 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(34): Show |
37 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.81-20231T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414796 | |||||||
| chr15:66414846 | G | C | 1 | a0001c0001t0002g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.81-20181G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414846 | |||||||
| chr15:66414850 | C | T | 40 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(37): Show |
40 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.81-20177C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414850 | |||||||
| chr15:66415269 | CT | C | 10 | a0001c0001t0001g0350 a0001c0001t0001g0352 a0001c0001t0001g0356 others(7): Show |
10 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.81-19756delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66415269 | ||||||
| chr15:66415353 | C | T | 2 | a0001c0001t0001g0223 a0001c0001t0001g0233 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.81-19674C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66415353 | |||||||
| chr15:66415458 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.81-19569C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66415458 | |||||||
| chr15:66415459 | C | T | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.81-19568C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66415459 | |||||||
| chr15:66415460 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-19567T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66415460 | |||||||
| chr15:66415523 | G | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(78): Show |
82 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.81-19504G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66415523 | |||||||
| chr15:66415987 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.81-19040C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66415987 | |||||||
| chr15:66416002 | C | T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-19025C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416002 | |||||||
| chr15:66416004 | C | A | 1 | a0001c0001t0003g0244 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.81-19023C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416004 | |||||||
| chr15:66416005 | C | T | 1 | a0001c0001t0003g0244 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.81-19022C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416005 | |||||||
| chr15:66416025 | G | C | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(1): Show |
4 | HG00735.hp1 HG01167.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-19002G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416025 | |||||||
| chr15:66416181 | T | TAGGGAGT others(23): Show |
1 | a0001c0001t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.81-18845_81-18816d others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66416181 | ||||||
| chr15:66416259 | ATTG | A | 4 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(1): Show |
4 | HG00140.hp1 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-18762_81-18760d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66416259 | ||||||
| chr15:66416271 | C | CTTG | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-18754_81-18752d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66416271 | ||||||
| chr15:66416370 | C | A | 1 | a0001c0001t0003g0193 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.81-18657C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416370 | |||||||
| chr15:66416409 | A | G | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81-18618A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416409 | |||||||
| chr15:66416437 | C | A | 28 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0213 others(25): Show |
28 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.81-18590C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416437 | |||||||
| chr15:66416467 | A | C | 38 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(35): Show |
38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.81-18560A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416467 | |||||||
| chr15:66416557 | G | C | 2 | a0001c0001t0001g0347 a0001c0001t0001g0348 |
2 | HG00733.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.81-18470G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416557 | |||||||
| chr15:66416601 | C | A | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.81-18426C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416601 | |||||||
| chr15:66416602 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-18425A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416602 | |||||||
| chr15:66416623 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.81-18404A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416623 | |||||||
| chr15:66417033 | C | T | 59 | a0001c0001t0002g0012 a0001c0001t0002g0048 a0001c0001t0002g0049 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.81-17994C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417033 | |||||||
| chr15:66417048 | C | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(308): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.81-17979C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417048 | |||||||
| chr15:66417316 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.81-17711T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417316 | |||||||
| chr15:66417320 | C | T | 2 | a0001c0001t0003g0164 a0001c0001t0003g0173 |
2 | HG03491.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.81-17707C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417320 | |||||||
| chr15:66417342 | G | A | 1 | a0001c0001t0003g0202 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.81-17685G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417342 | |||||||
| chr15:66417407 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(79): Show |
83 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.81-17620C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417407 | |||||||
| chr15:66417819 | A | G | 1 | a0001c0001t0006g0010 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.81-17208A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417819 | |||||||
| chr15:66417921 | C | G | 93 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(90): Show |
93 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.81-17106C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417921 | |||||||
| chr15:66417938 | C | T | 23 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0218 others(20): Show |
23 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.81-17089C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417938 | |||||||
| chr15:66418313 | C | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-16714C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66418313 | |||||||
| chr15:66418345 | T | C | 3 | a0001c0001t0001g0248 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.81-16682T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66418345 | |||||||
| chr15:66418447 | T | C | 4 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0315 others(1): Show |
4 | NA18967.hp1 NA18969.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-16580T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66418447 | |||||||
| chr15:66418552 | G | C | 1 | a0001c0001t0001g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.81-16475G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66418552 | |||||||
| chr15:66418555 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.81-16472C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66418555 | |||||||
| chr15:66418556 | G | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(308): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.81-16471G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66418556 | |||||||
| chr15:66418888 | C | T | 1 | a0001c0001t0003g0201 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.81-16139C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66418888 | |||||||
| chr15:66418945 | C | CT | 55 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0037 others(52): Show |
55 | HG00597.hp1 HG00673.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.81-16060dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66418945 | ||||||
| chr15:66418945 | C | CTT | 9 | a0001c0001t0001g0327 a0001c0001t0001g0329 a0001c0001t0001g0330 others(6): Show |
9 | HG00733.hp2 HG01109.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.81-16061_81-16060d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66418945 | ||||||
| chr15:66418945 | CT | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(104): Show |
108 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.81-16060delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66418945 | ||||||
| chr15:66419242 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.81-15785G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419242 | |||||||
| chr15:66419349 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.81-15678G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419349 | |||||||
| chr15:66419520 | CA | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-15494delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66419520 | ||||||
| chr15:66419531 | A | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0326 a0001c0001t0001g0328 others(1): Show |
4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-15496A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419531 | |||||||
| chr15:66419543 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.81-15484C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419543 | |||||||
| chr15:66419673 | G | T | 38 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(35): Show |
38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.81-15354G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419673 | |||||||
| chr15:66419704 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81-15323C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419704 | |||||||
| chr15:66419784 | CTGTT | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-15240_81-15237d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66419784 | ||||||
| chr15:66419899 | C | CA | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(308): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.81-15119dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66419899 | ||||||
| chr15:66419913 | G | A | 2 | a0001c0001t0001g0354 a0001c0001t0001g0355 |
2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.81-15114G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419913 | |||||||
| chr15:66419981 | AC | A | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.81-15045delC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419981 | |||||||
| chr15:66420042 | G | A | 30 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0214 others(27): Show |
30 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-14985G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420042 | |||||||
| chr15:66420154 | G | A | 1 | a0001c0004t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81-14873G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420154 | |||||||
| chr15:66420167 | C | T | 8 | a0001c0001t0003g0166 a0001c0001t0003g0172 a0001c0001t0003g0188 others(5): Show |
8 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.81-14860C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420167 | |||||||
| chr15:66420190 | A | G | 359 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(356): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.81-14837A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420190 | |||||||
| chr15:66420376 | G | T | 1 | a0001c0001t0003g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.81-14651G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420376 | |||||||
| chr15:66420384 | TG | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14641delG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420384 | ||||||
| chr15:66420451 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81-14576G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420451 | |||||||
| chr15:66420468 | A | C | 90 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0213 others(87): Show |
90 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.81-14559A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420468 | |||||||
| chr15:66420547 | T | A | 1 | a0001c0001t0005g0160 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.81-14480T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420547 | |||||||
| chr15:66420553 | AAAAAT | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14460_81-14456d others(7): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420553 | ||||||
| chr15:66420643 | A | G | 1 | a0001c0001t0003g0205 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.81-14384A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420643 | |||||||
| chr15:66420706 | C | CAT | 25 | a0001c0001t0001g0002 a0001c0001t0001g0139 a0001c0001t0001g0146 others(22): Show |
25 | HG00323.hp2 HG00597.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.81-14306_81-14305d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | ||||||
| chr15:66420706 | C | CATAT | 19 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(16): Show |
19 | HG00423.hp2 HG00609.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.81-14308_81-14305d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | ||||||
| chr15:66420706 | C | CATATAT | 13 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0124 others(10): Show |
13 | HG00621.hp2 HG02155.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.81-14310_81-14305d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | ||||||
| chr15:66420706 | C | CATATATA others(1): Show |
9 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0003g0176 others(6): Show |
9 | HG00099.hp1 HG00558.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.81-14312_81-14305d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | ||||||
| chr15:66420706 | C | CATATATA others(3): Show |
2 | a0001c0001t0001g0118 a0001c0001t0003g0163 |
2 | HG01515.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.81-14314_81-14305d others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | ||||||
| chr15:66420706 | C | CATATATA others(5): Show |
2 | a0001c0001t0002g0072 a0001c0001t0008g0073 |
2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.81-14316_81-14305d others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | ||||||
| chr15:66420706 | C | CATATATA others(7): Show |
2 | a0001c0001t0001g0238 a0001c0001t0003g0167 |
2 | HG01123.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.81-14318_81-14305d others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | ||||||
| chr15:66420706 | C | CATATATA others(9): Show |
3 | a0001c0001t0001g0279 a0001c0001t0003g0207 a0001c0001t0003g0244 |
3 | HG01106.hp2 HG03927.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.81-14320_81-14305d others(18): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | ||||||
| chr15:66420706 | C | CATATATA others(11): Show |
1 | a0001c0001t0003g0180 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(20): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | ||||||
| chr15:66420706 | C | CATATATA others(17): Show |
1 | a0001c0001t0001g0046 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(26): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | ||||||
| chr15:66420706 | C | CATATATA others(19): Show |
1 | a0001c0001t0001g0339 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | ||||||
| chr15:66420706 | C | CATATATA others(21): Show |
3 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0003g0182 |
3 | HG02486.hp1 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(30): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | ||||||
| chr15:66420706 | C | CATATATA others(25): Show |
1 | a0001c0001t0009g0165 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | ||||||
| chr15:66420715 | A | ATATATAT others(45): Show |
2 | a0001c0001t0001g0033 a0001c0001t0004g0028 |
2 | HG04204.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(54): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420715 | ||||||
| chr15:66420715 | A | ATATATAT others(39): Show |
2 | a0001c0001t0004g0020 a0001c0001t0004g0029 |
2 | NA18995.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(48): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420715 | ||||||
| chr15:66420715 | A | ATATATAT others(37): Show |
3 | a0001c0001t0004g0018 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | NA18944.hp1 NA18969.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(46): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420715 | ||||||
| chr15:66420715 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0334 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420715 | ||||||
| chr15:66420715 | A | ATATATAT others(31): Show |
2 | a0001c0001t0001g0246 a0001c0001t0004g0021 |
2 | NA18967.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(40): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420715 | ||||||
| chr15:66420715 | A | ATATATAT others(29): Show |
2 | a0001c0001t0001g0335 a0001c0001t0004g0041 |
2 | HG02004.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(38): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420715 | ||||||
| chr15:66420715 | ATATATAT others(1): Show |
A | 5 | a0001c0001t0006g0004 a0001c0001t0006g0005 a0001c0001t0006g0008 others(2): Show |
5 | HG01515.hp1 HG01517.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-14310_81-14303d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420715 | ||||||
| chr15:66420717 | A | ATATATAT others(43): Show |
2 | a0001c0001t0001g0307 a0001c0001t0004g0047 |
2 | NA19006.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(52): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420717 | ||||||
| chr15:66420717 | A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0040 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(46): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420717 | ||||||
| chr15:66420717 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420717 | ||||||
| chr15:66420719 | A | ATATATAT others(35): Show |
2 | a0001c0001t0001g0030 a0001c0001t0001g0045 |
2 | HG00738.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(44): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420719 | ||||||
| chr15:66420719 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0322 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(24): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420719 | ||||||
| chr15:66420719 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0323 a0001c0001t0001g0324 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(22): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420719 | ||||||
| chr15:66420721 | A | ATATATAT others(43): Show |
7 | a0001c0001t0001g0032 a0001c0001t0004g0017 a0001c0001t0004g0019 others(4): Show |
7 | HG00423.hp1 HG01106.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.81-14305_81-14304i others(52): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0117 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(43): Show |
3 | a0001c0001t0004g0022 a0001c0001t0004g0025 a0001c0001t0004g0147 |
3 | NA18959.hp2 NA19012.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(52): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(39): Show |
1 | a0001c0001t0001g0031 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(48): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0333 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(46): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(35): Show |
1 | a0001c0001t0004g0023 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(44): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0360 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(46): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0245 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(31): Show |
2 | a0001c0001t0001g0034 a0001c0001t0001g0038 |
2 | HG01123.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(40): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(27): Show |
4 | a0001c0001t0001g0328 a0001c0001t0001g0329 a0001c0001t0001g0344 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-14305_81-14304i others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(29): Show |
3 | a0001c0001t0001g0326 a0001c0001t0001g0349 a0001c0001t0001g0350 |
3 | HG02896.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(38): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(31): Show |
1 | a0001c0006t0001g0353 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(40): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0330 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(35): Show |
1 | a0001c0001t0001g0363 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(44): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0343 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(27): Show |
2 | a0001c0001t0001g0357 a0001c0001t0014g0212 |
2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(29): Show |
1 | a0001c0001t0013g0351 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(38): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0364 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(27): Show |
4 | a0001c0001t0001g0342 a0001c0001t0001g0347 a0001c0001t0001g0348 others(1): Show |
4 | HG00733.hp2 HG01069.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-14305_81-14304i others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0331 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(38): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0365 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0338 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(26): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(25): Show |
4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01261.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-14305_81-14304i others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0327 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0362 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0332 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0115 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(24): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0354 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(30): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0368 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(13): Show |
1 | a0001c0004t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(22): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0355 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(26): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0361 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(21): Show |
2 | a0001c0001t0001g0346 a0001c0001t0001g0366 |
2 | HG02895.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(30): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(23): Show |
2 | a0001c0001t0001g0367 a0001c0001t0001g0369 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0345 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0341 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(5): Show |
4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0141 others(1): Show |
4 | HG02622.hp1 NA18956.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-14305_81-14304i others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0143 |
2 | HG01993.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(5): Show |
11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0129 others(8): Show |
11 | HG00733.hp1 HG01257.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.81-14305_81-14304i others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0358 a0001c0001t0001g0359 |
2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(24): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0145 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420721 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.81-14306A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420721 | |||||||
| chr15:66420721 | ATG | A | 23 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0214 others(20): Show |
23 | HG01069.hp2 HG01071.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.81-14268_81-14267d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | ||||||
| chr15:66420723 | G | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.81-14304G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420723 | |||||||
| chr15:66420725 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.81-14302G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420725 | |||||||
| chr15:66420727 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.81-14300G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420727 | |||||||
| chr15:66420729 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(213): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.81-14298G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420729 | |||||||
| chr15:66420731 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(199): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.81-14296G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420731 | |||||||
| chr15:66420733 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(153): Show |
157 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.81-14294G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420733 | |||||||
| chr15:66420735 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(130): Show |
134 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.81-14292G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420735 | |||||||
| chr15:66420737 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(86): Show |
90 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.81-14290G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420737 | |||||||
| chr15:66420739 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(72): Show |
76 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.81-14288G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420739 | |||||||
| chr15:66420741 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0249 a0001c0001t0001g0250 others(50): Show |
53 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.81-14286G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420741 | |||||||
| chr15:66420743 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0249 a0001c0001t0001g0252 others(15): Show |
18 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.81-14284G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420743 | |||||||
| chr15:66420745 | G | A | 4 | a0001c0001t0001g0238 a0001c0001t0001g0249 a0001c0001t0001g0260 others(1): Show |
4 | HG00544.hp1 HG01123.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-14282G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420745 | |||||||
| chr15:66420747 | G | A | 2 | a0001c0001t0001g0238 a0001c0002t0001g0297 |
2 | HG00544.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.81-14280G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420747 | |||||||
| chr15:66420749 | G | A | 1 | a0001c0002t0001g0297 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.81-14278G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420749 | |||||||
| chr15:66420755 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.81-14272G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420755 | |||||||
| chr15:66420757 | G | A | 45 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(42): Show |
45 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.81-14270G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420757 | |||||||
| chr15:66420757 | GTGTA | G | 3 | a0001c0001t0005g0157 a0001c0001t0005g0239 a0001c0001t0005g0241 |
3 | HG00280.hp1 NA18963.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.81-14266_81-14263d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420757 | ||||||
| chr15:66420759 | G | A | 111 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(108): Show |
111 | HG00423.hp1 HG00733.hp2 HG00738.hp2 others(108): Show |
intron_variant | MODIFIER | c.81-14268G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420759 | |||||||
| chr15:66420759 | G | GTATA | 20 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0120 others(17): Show |
20 | HG00733.hp1 HG01257.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.81-14265_81-14264i others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420759 | ||||||
| chr15:66420759 | GTA | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0251 a0001c0001t0001g0253 others(19): Show |
23 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.81-14266_81-14265d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420759 | ||||||
| chr15:66420759 | GTATGTGT others(3): Show |
G | 40 | a0001c0001t0001g0213 a0001c0001t0002g0012 a0001c0001t0002g0049 others(37): Show |
40 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.81-14264_81-14255d others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420759 | ||||||
| chr15:66420759 | GTATGTGT others(5): Show |
G | 1 | a0001c0001t0006g0003 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.81-14264_81-14253d others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420759 | ||||||
| chr15:66420759 | GTATGTGT others(9): Show |
G | 1 | a0001c0001t0001g0306 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.81-14266_81-14251d others(18): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420759 | ||||||
| chr15:66420761 | A | G | 152 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(149): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.81-14266A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420761 | |||||||
| chr15:66420763 | G | A | 2 | a0001c0001t0002g0072 a0001c0001t0008g0073 |
2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.81-14264G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420763 | |||||||
| chr15:66420763 | GTGTGTAT others(1): Show |
G | 12 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0002g0054 others(9): Show |
12 | HG00544.hp2 HG00597.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.81-14262_81-14255d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420763 | ||||||
| chr15:66420765 | GTGTATA | G | 4 | a0001c0001t0002g0096 a0001c0001t0002g0100 a0001c0001t0002g0148 others(1): Show |
4 | HG00558.hp2 HG01074.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-14260_81-14255d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420765 | ||||||
| chr15:66420765 | GTGTATAT others(3): Show |
G | 1 | a0001c0001t0001g0298 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.81-14258_81-14249d others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420765 | ||||||
| chr15:66420767 | GTATA | G | 26 | a0001c0001t0001g0247 a0001c0001t0001g0256 a0001c0001t0001g0257 others(23): Show |
26 | HG00609.hp1 HG00639.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.81-14254_81-14251d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420767 | ||||||
| chr15:66420767 | GTATATA | G | 12 | a0001c0001t0001g0265 a0001c0001t0001g0272 a0001c0001t0001g0280 others(9): Show |
12 | HG00280.hp2 HG00639.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.81-14256_81-14251d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420767 | ||||||
| chr15:66420767 | GTATATAT others(1): Show |
G | 3 | a0001c0001t0001g0300 a0001c0001t0003g0182 a0001c0001t0009g0165 |
3 | HG02486.hp1 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.81-14258_81-14251d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420767 | ||||||
| chr15:66420769 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(99): Show |
103 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.81-14258A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420769 | |||||||
| chr15:66420771 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.81-14256A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420771 | |||||||
| chr15:66420773 | A | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(119): Show |
123 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.81-14254A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420773 | |||||||
| chr15:66420775 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(145): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.81-14252A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420775 | |||||||
| chr15:66420777 | G | A | 2 | a0001c0001t0002g0072 a0001c0001t0008g0073 |
2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.81-14250G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420777 | |||||||
| chr15:66420779 | G | GTA | 28 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0215 others(25): Show |
28 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.81-14240_81-14239d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420779 | ||||||
| chr15:66420779 | G | GTATATAT others(23): Show |
1 | a0001c0001t0001g0338 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.81-14240_81-14239i others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420779 | ||||||
| chr15:66420779 | G | GTATATAT others(79): Show |
1 | a0001c0001t0001g0339 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.81-14240_81-14239i others(88): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420779 | ||||||
| chr15:66420781 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.81-14246A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420781 | |||||||
| chr15:66420783 | A | G | 6 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(3): Show |
6 | HG00558.hp1 HG00673.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-14244A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420783 | |||||||
| chr15:66420787 | ATG | A | 13 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(10): Show |
13 | HG00280.hp1 HG00438.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.81-14234_81-14233d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420787 | ||||||
| chr15:66420789 | G | A | 119 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0031 others(116): Show |
119 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.81-14238G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420789 | |||||||
| chr15:66420791 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(77): Show |
81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.81-14236G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420791 | |||||||
| chr15:66420793 | G | A | 48 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0119 others(45): Show |
48 | HG00609.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.81-14234G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420793 | |||||||
| chr15:66420793 | G | GTATATAT others(7): Show |
36 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(33): Show |
36 | HG00733.hp2 HG01069.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.81-14226_81-14213d others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420793 | ||||||
| chr15:66420801 | A | ATG | 21 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0120 others(18): Show |
21 | HG00733.hp1 HG01257.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.81-14222_81-14221d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420801 | ||||||
| chr15:66420801 | A | G | 2 | a0001c0001t0001g0336 a0001c0001t0002g0066 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.81-14226A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420801 | |||||||
| chr15:66420803 | G | A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0231 a0001c0001t0001g0233 |
3 | HG02451.hp2 HG02970.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.81-14224G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420803 | |||||||
| chr15:66420805 | G | A | 39 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(36): Show |
39 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.81-14222G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420805 | |||||||
| chr15:66420805 | G | GTA | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.81-14214_81-14213d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420805 | ||||||
| chr15:66420807 | A | G | 2 | a0001c0001t0001g0223 a0001c0001t0001g0233 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.81-14220A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420807 | |||||||
| chr15:66420809 | A | G | 2 | a0001c0001t0001g0231 a0001c0001t0002g0066 |
2 | HG01243.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.81-14218A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420809 | |||||||
| chr15:66420815 | G | A | 4 | a0001c0001t0001g0338 a0001c0001t0001g0339 a0001c0001t0001g0362 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-14212G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420815 | |||||||
| chr15:66420817 | GTA | G | 6 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-14200_81-14199d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420817 | ||||||
| chr15:66420819 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(91): Show |
95 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.81-14208A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420819 | |||||||
| chr15:66420823 | A | G | 220 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0031 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.81-14204A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420823 | |||||||
| chr15:66420823 | ATATATGT others(11): Show |
A | 2 | a0001c0001t0006g0008 a0001c0001t0006g0009 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.81-14202_81-14185d others(20): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420823 | ||||||
| chr15:66420833 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0365 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.81-14187_81-14186i others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420833 | ||||||
| chr15:66420833 | A | ATATGTAT others(5): Show |
10 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0123 others(7): Show |
10 | HG00609.hp2 HG01361.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.81-14191_81-14190i others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420833 | ||||||
| chr15:66420833 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.81-14194A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420833 | |||||||
| chr15:66420837 | A | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(77): Show |
81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.81-14190A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420837 | |||||||
| chr15:66420837 | ATATG | A | 6 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-14188_81-14185d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420837 | ||||||
| chr15:66420839 | ATG | A | 79 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0120 others(76): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.81-14182_81-14181d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420839 | ||||||
| chr15:66420841 | G | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(225): Show |
229 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.81-14186G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420841 | |||||||
| chr15:66420847 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81-14180A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420847 | |||||||
| chr15:66420853 | A | G | 3 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0340 |
3 | HG02109.hp1 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.81-14174A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420853 | |||||||
| chr15:66420855 | G | A | 1 | a0001c0001t0001g0362 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.81-14172G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420855 | |||||||
| chr15:66420855 | GTGTGTAT others(27): Show |
G | 1 | a0001c0001t0002g0066 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81-14170_81-14137d others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420855 | ||||||
| chr15:66420857 | GTGTATA | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14168_81-14163d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420857 | ||||||
| chr15:66420859 | GTA | G | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.81-14160_81-14159d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420859 | ||||||
| chr15:66420861 | A | G | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(307): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.81-14166A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420861 | |||||||
| chr15:66420867 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.81-14160A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420867 | |||||||
| chr15:66420873 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14154G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420873 | |||||||
| chr15:66420874 | T | C | 1 | a0001c0001t0003g0196 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.81-14153T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420874 | |||||||
| chr15:66420875 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0362 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.81-14141_81-14140i others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420875 | ||||||
| chr15:66420881 | A | G | 1 | a0001c0001t0001g0339 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.81-14146A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420881 | |||||||
| chr15:66420881 | ATGTG | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14144_81-14141d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420881 | ||||||
| chr15:66420886 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14141T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420886 | |||||||
| chr15:66420894 | CACAT | C | 15 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(12): Show |
15 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.81-14121_81-14118d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420894 | ||||||
| chr15:66420896 | C | T | 1 | a0001c0001t0002g0149 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.81-14131C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420896 | |||||||
| chr15:66420906 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0267 |
2 | HG01978.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.81-14121T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420906 | |||||||
| chr15:66420912 | CACAT | C | 109 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(106): Show |
109 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.81-14105_81-14102d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420912 | ||||||
| chr15:66420916 | T | C | 2 | a0001c0001t0002g0076 a0001c0001t0002g0097 |
2 | HG00597.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.81-14111T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420916 | |||||||
| chr15:66420922 | CAT | C | 5 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0003g0167 others(2): Show |
5 | HG03130.hp2 NA18940.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-14097_81-14096d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420922 | ||||||
| chr15:66420940 | C | CAT | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14081_81-14080d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420940 | ||||||
| chr15:66420950 | TACAC | T | 3 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0065 |
3 | NA18946.hp2 NA19056.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.81-14075_81-14072d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420950 | ||||||
| chr15:66420958 | C | CAT | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14063_81-14062d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420958 | ||||||
| chr15:66420962 | TATACAC | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(106): Show |
110 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.81-14063_81-14058d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420962 | ||||||
| chr15:66420962 | TATACACA others(7): Show |
T | 1 | a0001c0001t0003g0169 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.81-14045_81-14032d others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420962 | ||||||
| chr15:66420970 | CACAT | C | 160 | a0001c0001t0001g0046 a0001c0001t0001g0111 a0001c0001t0001g0112 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.81-14049_81-14046d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420970 | ||||||
| chr15:66420974 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(107): Show |
111 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.81-14053T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420974 | |||||||
| chr15:66420974 | TACATACA others(1): Show |
T | 40 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0031 others(37): Show |
40 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.81-14049_81-14042d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420974 | ||||||
| chr15:66420976 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81-14051C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420976 | |||||||
| chr15:66420984 | C | T | 2 | a0001c0001t0002g0061 a0001c0001t0002g0070 |
2 | HG00099.hp2 HG00140.hp2 |
intron_variant | MODIFIER | c.81-14043C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420984 | |||||||
| chr15:66420984 | CACAT | C | 4 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
4 | HG03041.hp2 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-14033_81-14030d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420984 | ||||||
| chr15:66420988 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0003g0198 |
2 | HG01993.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.81-14039T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420988 | |||||||
| chr15:66420995 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14032A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420995 | |||||||
| chr15:66421005 | G | T | 1 | a0001c0001t0001g0325 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.81-14022G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421005 | |||||||
| chr15:66421019 | T | TTA | 359 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(356): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.81-14005_81-14004d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421019 | ||||||
| chr15:66421083 | TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.81-13934_81-13921d others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421083 | ||||||
| chr15:66421083 | TACACACA others(19): Show |
T | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.81-13934_81-13909d others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421083 | ||||||
| chr15:66421093 | T | C | 1 | a0001c0001t0002g0340 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.81-13934T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421093 | |||||||
| chr15:66421093 | T | TAC | 11 | a0001c0001t0001g0046 a0001c0001t0001g0116 a0001c0001t0003g0209 others(8): Show |
11 | HG00280.hp1 HG00280.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.81-13902_81-13901d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | ||||||
| chr15:66421093 | T | TACAC | 6 | a0001c0001t0005g0160 a0001c0001t0005g0161 a0001c0001t0005g0240 others(3): Show |
6 | HG01074.hp1 HG01099.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.81-13904_81-13901d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | ||||||
| chr15:66421093 | T | TACACAC | 3 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0243 |
3 | HG00438.hp2 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.81-13906_81-13901d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | ||||||
| chr15:66421093 | TACAC | T | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.81-13904_81-13901d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | ||||||
| chr15:66421093 | TACACAC | T | 12 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(9): Show |
12 | HG00738.hp2 HG01106.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.81-13906_81-13901d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | ||||||
| chr15:66421093 | TACACACA others(1): Show |
T | 26 | a0001c0001t0001g0038 a0001c0001t0001g0109 a0001c0001t0001g0245 others(23): Show |
26 | HG00423.hp1 HG01099.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.81-13908_81-13901d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | ||||||
| chr15:66421093 | TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.81-13910_81-13901d others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | ||||||
| chr15:66421093 | TACACACA others(7): Show |
T | 38 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(35): Show |
38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.81-13914_81-13901d others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | ||||||
| chr15:66421107 | CACACACA others(15): Show |
C | 1 | a0001c0001t0003g0164 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.81-13918_81-13897d others(24): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421107 | ||||||
| chr15:66421117 | CACACACA others(3): Show |
C | 3 | a0001c0001t0001g0213 a0001c0001t0001g0273 a0001c0001t0002g0099 |
3 | HG02280.hp1 HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.81-13908_81-13899d others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421117 | ||||||
| chr15:66421119 | CACACACA others(1): Show |
C | 7 | a0001c0001t0001g0261 a0001c0001t0001g0270 a0001c0001t0001g0275 others(4): Show |
7 | HG02027.hp1 HG03834.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.81-13906_81-13899d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421119 | ||||||
| chr15:66421121 | CACACAT | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(120): Show |
123 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.81-13904_81-13899d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421121 | ||||||
| chr15:66421123 | CACAT | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0111 others(54): Show |
58 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.81-13902_81-13899d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421123 | ||||||
| chr15:66421123 | CACATAT | C | 3 | a0001c0001t0002g0340 a0001c0001t0003g0370 a0001c0001t0003g0371 |
3 | HG00323.hp2 HG01074.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.81-13902_81-13897d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421123 | ||||||
| chr15:66421125 | CAT | C | 40 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0236 others(37): Show |
40 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.81-13888_81-13887d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421125 | ||||||
| chr15:66421125 | CATAT | C | 10 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0003g0179 others(7): Show |
10 | HG00099.hp1 HG02109.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.81-13890_81-13887d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421125 | ||||||
| chr15:66421127 | T | C | 34 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(31): Show |
34 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.81-13900T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421127 | |||||||
| chr15:66421129 | T | C | 50 | a0001c0001t0003g0163 a0001c0001t0003g0166 a0001c0001t0003g0167 others(47): Show |
50 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.81-13898T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421129 | |||||||
| chr15:66421228 | C | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-13799C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421228 | |||||||
| chr15:66421295 | C | A | 30 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0214 others(27): Show |
30 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-13732C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421295 | |||||||
| chr15:66421378 | C | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-13649C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421378 | |||||||
| chr15:66421438 | A | G | 2 | a0001c0001t0001g0287 a0001c0001t0001g0299 |
2 | HG00609.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.81-13589A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421438 | |||||||
| chr15:66421619 | G | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-13408G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421619 | |||||||
| chr15:66421683 | C | G | 41 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(38): Show |
41 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.81-13344C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421683 | |||||||
| chr15:66421704 | G | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-13323G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421704 | |||||||
| chr15:66421883 | C | CT | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(242): Show |
246 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.81-13131dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421883 | ||||||
| chr15:66422040 | C | G | 59 | a0001c0001t0001g0213 a0001c0001t0002g0012 a0001c0001t0002g0048 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.81-12987C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422040 | |||||||
| chr15:66422405 | A | G | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.81-12622A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422405 | |||||||
| chr15:66422507 | C | T | 7 | a0001c0001t0001g0261 a0001c0001t0001g0270 a0001c0001t0001g0309 others(4): Show |
7 | HG02027.hp1 HG02040.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.81-12520C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422507 | |||||||
| chr15:66422584 | C | T | 1 | a0001c0001t0001g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.81-12443C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422584 | |||||||
| chr15:66422614 | A | G | 6 | a0001c0001t0003g0166 a0001c0001t0003g0172 a0001c0001t0003g0188 others(3): Show |
6 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.81-12413A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422614 | |||||||
| chr15:66422645 | G | A | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.81-12382G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422645 | |||||||
| chr15:66422820 | C | T | 2 | a0001c0001t0001g0354 a0001c0001t0001g0355 |
2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.81-12207C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422820 | |||||||
| chr15:66422826 | C | T | 1 | a0001c0001t0002g0085 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.81-12201C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422826 | |||||||
| chr15:66422867 | C | T | 1 | a0001c0001t0003g0168 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.81-12160C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422867 | |||||||
| chr15:66422920 | CT | C | 13 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(10): Show |
13 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.81-12098delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66422920 | ||||||
| chr15:66422962 | T | C | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81-12065T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422962 | |||||||
| chr15:66423211 | C | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-11816C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423211 | |||||||
| chr15:66423284 | A | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-11743A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423284 | |||||||
| chr15:66423335 | A | C | 1 | a0001c0001t0002g0091 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.81-11692A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423335 | |||||||
| chr15:66423339 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.81-11688T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423339 | |||||||
| chr15:66423407 | T | C | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(359): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.81-11620T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423407 | |||||||
| chr15:66423442 | C | CT | 11 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(8): Show |
11 | HG01255.hp1 HG01261.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.81-11571dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66423442 | ||||||
| chr15:66423442 | CT | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(108): Show |
112 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.81-11571delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66423442 | ||||||
| chr15:66423604 | A | AT | 281 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(278): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.81-11403dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66423604 | ||||||
| chr15:66423604 | A | ATT | 19 | a0001c0001t0001g0032 a0001c0001t0001g0109 a0001c0001t0001g0145 others(16): Show |
19 | HG00642.hp2 HG00673.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.81-11404_81-11403d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66423604 | ||||||
| chr15:66423604 | A | ATTT | 42 | a0001c0001t0001g0011 a0001c0001t0001g0326 a0001c0001t0001g0327 others(39): Show |
42 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.81-11405_81-11403d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66423604 | ||||||
| chr15:66423738 | G | A | 41 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(38): Show |
41 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.81-11289G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423738 | |||||||
| chr15:66423755 | G | GC | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(308): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.81-11271dupC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66423755 | ||||||
| chr15:66423764 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-11263T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423764 | |||||||
| chr15:66423768 | C | T | 51 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(48): Show |
51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.81-11259C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423768 | |||||||
| chr15:66423807 | A | G | 1 | a0001c0001t0010g0190 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.81-11220A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423807 | |||||||
| chr15:66423885 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.81-11142G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423885 | |||||||
| chr15:66423983 | C | T | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(1): Show |
4 | HG00735.hp1 HG01167.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-11044C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423983 | |||||||
| chr15:66424014 | A | C | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(1): Show |
4 | HG00735.hp1 HG01167.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-11013A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424014 | |||||||
| chr15:66424043 | G | A | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.81-10984G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424043 | |||||||
| chr15:66424064 | A | AT | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.81-10953dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66424064 | ||||||
| chr15:66424064 | A | T | 1 | a0001c0001t0001g0327 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.81-10963A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424064 | |||||||
| chr15:66424101 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.81-10926A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424101 | |||||||
| chr15:66424102 | T | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.81-10925T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424102 | |||||||
| chr15:66424111 | G | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.81-10916G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424111 | |||||||
| chr15:66424348 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.81-10679G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424348 | |||||||
| chr15:66424358 | C | T | 3 | a0001c0001t0003g0167 a0001c0001t0003g0209 a0001c0001t0009g0165 |
3 | NA18940.hp1 NA18962.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.81-10669C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424358 | |||||||
| chr15:66424383 | T | G | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(359): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.81-10644T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424383 | |||||||
| chr15:66424583 | C | T | 59 | a0001c0001t0001g0213 a0001c0001t0002g0012 a0001c0001t0002g0048 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.81-10444C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424583 | |||||||
| chr15:66424603 | C | A | 2 | a0001c0001t0005g0160 a0001c0001t0005g0161 |
2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.81-10424C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424603 | |||||||
| chr15:66424791 | C | CT | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(134): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.81-10213dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66424791 | ||||||
| chr15:66424791 | C | CTT | 6 | a0001c0001t0001g0298 a0001c0001t0003g0204 a0001c0001t0003g0244 others(3): Show |
6 | HG01074.hp1 HG01099.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-10214_81-10213d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66424791 | ||||||
| chr15:66424791 | CT | C | 24 | a0001c0001t0001g0112 a0001c0001t0001g0129 a0001c0001t0001g0139 others(21): Show |
24 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.81-10213delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66424791 | ||||||
| chr15:66424791 | CTT | C | 9 | a0001c0001t0001g0233 a0001c0001t0002g0061 a0001c0001t0002g0070 others(6): Show |
9 | HG00099.hp2 HG00140.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.81-10214_81-10213d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66424791 | ||||||
| chr15:66424791 | CTTT | C | 48 | a0001c0001t0001g0213 a0001c0001t0002g0012 a0001c0001t0002g0048 others(45): Show |
48 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.81-10215_81-10213d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66424791 | ||||||
| chr15:66424791 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0248 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.81-10224_81-10213d others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66424791 | ||||||
| chr15:66424816 | C | A | 359 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(356): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.81-10211C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424816 | |||||||
| chr15:66425002 | G | A | 1 | a0001c0001t0001g0338 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.81-10025G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425002 | |||||||
| chr15:66425042 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.81-9985C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425042 | |||||||
| chr15:66425383 | AT | A | 10 | a0001c0001t0001g0326 a0001c0001t0003g0174 a0001c0001t0006g0003 others(7): Show |
10 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.81-9633delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66425383 | ||||||
| chr15:66425408 | A | G | 4 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-9619A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425408 | |||||||
| chr15:66425417 | G | A | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG01099.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.81-9610G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425417 | |||||||
| chr15:66425446 | C | G | 1 | a0001c0001t0005g0159 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.81-9581C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425446 | |||||||
| chr15:66425482 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.81-9545A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425482 | |||||||
| chr15:66425915 | C | T | 2 | a0001c0001t0001g0360 a0001c0006t0001g0353 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.81-9112C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425915 | |||||||
| chr15:66425929 | T | A | 1 | a0001c0001t0003g0202 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.81-9098T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425929 | |||||||
| chr15:66425931 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81-9096G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425931 | |||||||
| chr15:66426049 | A | G | 30 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0341 others(27): Show |
30 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-8978A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426049 | |||||||
| chr15:66426142 | CT | C | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(304): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.81-8869delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66426142 | ||||||
| chr15:66426142 | CTT | C | 52 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(49): Show |
52 | HG00423.hp1 HG00738.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.81-8870_81-8869del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66426142 | ||||||
| chr15:66426151 | T | A | 89 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0213 others(86): Show |
89 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.81-8876T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426151 | |||||||
| chr15:66426313 | T | G | 1 | a0001c0001t0014g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.81-8714T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426313 | |||||||
| chr15:66426360 | C | CA | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(249): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.81-8653dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66426360 | ||||||
| chr15:66426360 | C | CAA | 58 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(55): Show |
58 | HG00140.hp1 HG00423.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.81-8654_81-8653dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66426360 | ||||||
| chr15:66426360 | C | CAAA | 8 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0046 others(5): Show |
8 | HG01433.hp1 HG02055.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.81-8655_81-8653dup others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66426360 | ||||||
| chr15:66426375 | C | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.81-8652C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426375 | |||||||
| chr15:66426416 | A | G | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-8611A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426416 | |||||||
| chr15:66426606 | T | G | 1 | a0001c0001t0002g0150 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.81-8421T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426606 | |||||||
| chr15:66426643 | G | C | 1 | a0001c0001t0001g0339 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.81-8384G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426643 | |||||||
| chr15:66426695 | G | A | 48 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(45): Show |
48 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.81-8332G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426695 | |||||||
| chr15:66426792 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.81-8235T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426792 | |||||||
| chr15:66426844 | A | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(79): Show |
83 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.81-8183A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426844 | |||||||
| chr15:66426880 | T | G | 1 | a0001c0001t0002g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.81-8147T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426880 | |||||||
| chr15:66426931 | T | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(294): Show |
298 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.81-8096T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426931 | |||||||
| chr15:66426943 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(78): Show |
82 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.81-8084G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426943 | |||||||
| chr15:66427030 | T | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0131 |
2 | NA18953.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.81-7997T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66427030 | |||||||
| chr15:66427067 | T | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0131 |
2 | NA18953.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.81-7960T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66427067 | |||||||
| chr15:66427355 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0326 a0001c0001t0001g0328 others(1): Show |
4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-7672C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66427355 | |||||||
| chr15:66427386 | C | T | 31 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(28): Show |
31 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.81-7641C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66427386 | |||||||
| chr15:66427756 | C | T | 8 | a0001c0001t0001g0261 a0001c0001t0001g0270 a0001c0001t0001g0307 others(5): Show |
8 | HG02027.hp1 HG02040.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-7271C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66427756 | |||||||
| chr15:66427970 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81-7057C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66427970 | |||||||
| chr15:66428011 | C | G | 1 | a0001c0001t0002g0096 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.81-7016C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428011 | |||||||
| chr15:66428075 | C | G | 1 | a0001c0001t0003g0197 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.81-6952C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428075 | |||||||
| chr15:66428098 | C | T | 1 | a0001c0001t0014g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.81-6929C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428098 | |||||||
| chr15:66428271 | C | CGTGTGTG others(3): Show |
1 | a0001c0001t0001g0342 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.81-6711_81-6702dup others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | ||||||
| chr15:66428271 | CGT | C | 31 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0039 others(28): Show |
31 | HG01169.hp1 HG01243.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.81-6703_81-6702del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | ||||||
| chr15:66428271 | CGTGT | C | 42 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0125 others(39): Show |
42 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.81-6705_81-6702del others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | ||||||
| chr15:66428271 | CGTGTGT | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0030 others(85): Show |
89 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.81-6707_81-6702del others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | ||||||
| chr15:66428271 | CGTGTGTG others(1): Show |
C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0035 a0001c0001t0001g0036 others(72): Show |
75 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.81-6709_81-6702del others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | ||||||
| chr15:66428271 | CGTGTGTG others(3): Show |
C | 28 | a0001c0001t0001g0046 a0001c0001t0001g0118 a0001c0001t0001g0227 others(25): Show |
28 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.81-6711_81-6702del others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | ||||||
| chr15:66428271 | CGTGTGTG others(5): Show |
C | 44 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(41): Show |
44 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.81-6713_81-6702del others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | ||||||
| chr15:66428271 | CGTGTGTG others(7): Show |
C | 12 | a0001c0001t0001g0107 a0001c0001t0001g0112 a0001c0001t0001g0218 others(9): Show |
12 | HG02165.hp2 HG02559.hp1 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.81-6715_81-6702del others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | ||||||
| chr15:66428271 | CGTGTGTG others(9): Show |
C | 20 | a0001c0001t0001g0111 a0001c0001t0001g0219 a0001c0001t0001g0220 others(17): Show |
20 | HG00558.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.81-6717_81-6702del others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | ||||||
| chr15:66428271 | CGTGTGTG others(21): Show |
C | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81-6729_81-6702del others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | ||||||
| chr15:66428271 | CGTGTGTG others(27): Show |
C | 2 | a0001c0001t0005g0157 a0001c0001t0005g0159 |
2 | HG00280.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.81-6735_81-6702del others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | ||||||
| chr15:66428275 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.81-6752T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428275 | |||||||
| chr15:66428279 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.81-6748T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428279 | |||||||
| chr15:66428281 | T | C | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0141 others(1): Show |
4 | NA18953.hp1 NA18956.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-6746T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428281 | |||||||
| chr15:66428283 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0142 |
2 | NA18968.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.81-6744T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428283 | |||||||
| chr15:66428285 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.81-6742T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428285 | |||||||
| chr15:66428388 | G | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-6639G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428388 | |||||||
| chr15:66428699 | T | C | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-6328T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428699 | |||||||
| chr15:66428773 | C | CT | 31 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0117 others(28): Show |
31 | HG00609.hp1 HG00673.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.81-6228dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428773 | ||||||
| chr15:66428773 | C | CTT | 9 | a0001c0001t0001g0011 a0001c0001t0001g0331 a0001c0001t0001g0332 others(6): Show |
9 | HG00733.hp2 HG01515.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.81-6229_81-6228dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428773 | ||||||
| chr15:66428773 | C | CTTT | 18 | a0001c0001t0001g0325 a0001c0001t0001g0327 a0001c0001t0001g0342 others(15): Show |
18 | HG00639.hp1 HG01109.hp1 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.81-6230_81-6228dup others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428773 | ||||||
| chr15:66428773 | C | CTTTT | 10 | a0001c0001t0001g0156 a0001c0001t0001g0360 a0001c0001t0001g0361 others(7): Show |
10 | HG00280.hp2 HG01891.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.81-6231_81-6228dup others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428773 | ||||||
| chr15:66428773 | CT | C | 148 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0031 others(145): Show |
148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.81-6228delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428773 | ||||||
| chr15:66428773 | CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(3): Show |
6 | HG02559.hp2 HG02895.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.81-6235_81-6228del others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428773 | ||||||
| chr15:66428840 | C | T | 10 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0159 others(7): Show |
10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.81-6187C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428840 | |||||||
| chr15:66428865 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(79): Show |
83 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.81-6162C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428865 | |||||||
| chr15:66428866 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-6161G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428866 | |||||||
| chr15:66428889 | C | T | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.81-6138C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428889 | |||||||
| chr15:66428936 | C | T | 2 | a0001c0001t0001g0285 a0001c0001t0001g0301 |
2 | NA18947.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.81-6091C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428936 | |||||||
| chr15:66428937 | G | A | 37 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(34): Show |
37 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.81-6090G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428937 | |||||||
| chr15:66428954 | A | G | 36 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(33): Show |
36 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.81-6073A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428954 | |||||||
| chr15:66429193 | G | A | 9 | a0001c0001t0001g0314 a0001c0001t0006g0003 a0001c0001t0006g0004 others(6): Show |
9 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.81-5834G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429193 | |||||||
| chr15:66429278 | CAA | C | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.81-5748_81-5747del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429278 | |||||||
| chr15:66429300 | G | T | 1 | a0001c0001t0002g0151 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.81-5727G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429300 | |||||||
| chr15:66429342 | A | G | 4 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-5685A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429342 | |||||||
| chr15:66429350 | ACT | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-5676_81-5675del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429350 | |||||||
| chr15:66429439 | T | C | 2 | a0001c0001t0005g0240 a0001c0001t0005g0243 |
2 | HG00438.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.81-5588T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429439 | |||||||
| chr15:66429517 | A | G | 64 | a0001c0001t0001g0213 a0001c0001t0001g0358 a0001c0001t0001g0359 others(61): Show |
64 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.81-5510A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429517 | |||||||
| chr15:66429518 | T | C | 1 | a0001c0001t0006g0010 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.81-5509T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429518 | |||||||
| chr15:66429666 | CCCCCCCC others(7): Show |
C | 35 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(32): Show |
35 | HG00423.hp1 HG01099.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.81-5353_81-5340del others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66429666 | ||||||
| chr15:66429667 | CCCCCCCC others(6): Show |
C | 4 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0045 others(1): Show |
4 | HG00738.hp2 HG01243.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-5352_81-5340del others(13): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66429667 | ||||||
| chr15:66429675 | C | G | 2 | a0001c0001t0006g0007 a0001c0001t0006g0009 |
2 | HG00280.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.81-5352C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429675 | |||||||
| chr15:66429676 | C | A | 6 | a0001c0001t0001g0350 a0001c0001t0001g0352 a0001c0001t0001g0356 others(3): Show |
6 | HG02055.hp2 HG02280.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-5351C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429676 | |||||||
| chr15:66429676 | C | G | 9 | a0001c0001t0001g0339 a0001c0001t0001g0346 a0001c0001t0001g0347 others(6): Show |
9 | HG01069.hp1 HG01517.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.81-5351C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429676 | |||||||
| chr15:66429676 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0120 a0001c0001t0001g0121 others(39): Show |
42 | HG00423.hp2 HG00438.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.81-5351C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429676 | |||||||
| chr15:66429677 | C | A | 4 | a0001c0001t0001g0290 a0001c0001t0001g0357 a0001c0001t0001g0360 others(1): Show |
4 | HG02056.hp1 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-5350C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429677 | |||||||
| chr15:66429677 | C | G | 29 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0115 others(26): Show |
29 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.81-5350C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429677 | |||||||
| chr15:66429677 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(65): Show |
68 | HG00609.hp1 HG00609.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.81-5350C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429677 | |||||||
| chr15:66429678 | C | A | 2 | a0001c0001t0001g0289 a0001c0001t0001g0364 |
2 | HG01891.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.81-5349C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429678 | |||||||
| chr15:66429678 | C | CCCCG | 19 | a0001c0001t0001g0231 a0001c0001t0002g0012 a0001c0001t0002g0052 others(16): Show |
19 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.81-5349_81-5348ins others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429678 | |||||||
| chr15:66429678 | C | CCCG | 24 | a0001c0001t0001g0213 a0001c0001t0001g0233 a0001c0001t0001g0238 others(21): Show |
24 | HG00597.hp1 HG01074.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.81-5349_81-5348ins others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429678 | |||||||
| chr15:66429678 | C | CCG | 26 | a0001c0001t0001g0156 a0001c0001t0001g0219 a0001c0001t0001g0220 others(23): Show |
26 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.81-5349_81-5348ins others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429678 | |||||||
| chr15:66429678 | C | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0120 a0001c0001t0001g0121 others(56): Show |
59 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.81-5349C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429678 | |||||||
| chr15:66429678 | CG | C | 31 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0115 others(28): Show |
31 | HG00733.hp2 HG01074.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.81-5348delG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429678 | |||||||
| chr15:66429678 | CGT | C | 10 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0350 others(7): Show |
10 | HG01069.hp1 HG01515.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.81-5348_81-5347del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429678 | |||||||
| chr15:66429679 | G | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0117 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.81-5348G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429679 | |||||||
| chr15:66429679 | G | GC | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(108): Show |
111 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.81-5348_81-5347ins others(1): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429679 | |||||||
| chr15:66429679 | G | GCC | 9 | a0001c0001t0001g0118 a0001c0001t0001g0225 a0001c0001t0001g0235 others(6): Show |
9 | HG00438.hp2 HG01175.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.81-5348_81-5347ins others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429679 | |||||||
| chr15:66429680 | T | C | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(306): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.81-5347T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429680 | |||||||
| chr15:66429726 | G | A | 2 | a0001c0001t0001g0347 a0001c0001t0001g0348 |
2 | HG00733.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.81-5301G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429726 | |||||||
| chr15:66429867 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.81-5160T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429867 | |||||||
| chr15:66429913 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-5114A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429913 | |||||||
| chr15:66429969 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.81-5058C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429969 | |||||||
| chr15:66429979 | C | T | 3 | a0001c0001t0001g0248 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.81-5048C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429979 | |||||||
| chr15:66430005 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-5022C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430005 | |||||||
| chr15:66430231 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-4796G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430231 | |||||||
| chr15:66430287 | G | T | 1 | a0001c0001t0002g0051 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.81-4740G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430287 | |||||||
| chr15:66430534 | G | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-4493G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430534 | |||||||
| chr15:66430549 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81-4478C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430549 | |||||||
| chr15:66430608 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.81-4419A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430608 | |||||||
| chr15:66430715 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-4312T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430715 | |||||||
| chr15:66430936 | T | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-4091T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430936 | |||||||
| chr15:66430971 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.81-4056C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430971 | |||||||
| chr15:66431098 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.81-3929T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431098 | |||||||
| chr15:66431211 | C | T | 1 | a0001c0001t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.81-3816C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431211 | |||||||
| chr15:66431513 | G | A | 9 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0062 others(6): Show |
9 | HG00544.hp2 HG01884.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.81-3514G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431513 | |||||||
| chr15:66431587 | A | G | 1 | a0001c0001t0001g0362 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.81-3440A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431587 | |||||||
| chr15:66431655 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81-3372G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431655 | |||||||
| chr15:66431694 | G | T | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81-3333G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431694 | |||||||
| chr15:66431871 | G | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-3156G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431871 | |||||||
| chr15:66431890 | C | G | 1 | a0001c0001t0001g0275 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.81-3137C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431890 | |||||||
| chr15:66432008 | C | G | 1 | a0001c0001t0003g0184 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.81-3019C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432008 | |||||||
| chr15:66432012 | A | G | 90 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0213 others(87): Show |
90 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.81-3015A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432012 | |||||||
| chr15:66432232 | A | G | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(359): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.81-2795A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432232 | |||||||
| chr15:66432274 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-2753G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432274 | |||||||
| chr15:66432343 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.81-2684G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432343 | |||||||
| chr15:66432425 | A | G | 2 | a0001c0001t0005g0160 a0001c0001t0005g0161 |
2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.81-2602A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432425 | |||||||
| chr15:66432839 | A | G | 1 | a0001c0001t0002g0012 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.81-2188A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432839 | |||||||
| chr15:66432959 | A | AGT | 23 | a0001c0001t0001g0219 a0001c0001t0001g0221 a0001c0001t0001g0225 others(20): Show |
23 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.81-2027_81-2026dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | ||||||
| chr15:66432959 | A | AGTGT | 39 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(36): Show |
39 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.81-2029_81-2026dup others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | ||||||
| chr15:66432959 | A | AGTGTGT | 77 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(74): Show |
77 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.81-2031_81-2026dup others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | ||||||
| chr15:66432959 | A | AGTGTGTG others(1): Show |
56 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0140 others(53): Show |
57 | HG00280.hp2 HG00323.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.81-2033_81-2026dup others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | ||||||
| chr15:66432959 | A | AGTGTGTG others(3): Show |
44 | a0001c0001t0001g0109 a0001c0001t0001g0120 a0001c0001t0001g0133 others(41): Show |
44 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.81-2035_81-2026dup others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | ||||||
| chr15:66432959 | A | AGTGTGTG others(5): Show |
39 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0118 others(36): Show |
39 | HG00544.hp1 HG00621.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.81-2037_81-2026dup others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | ||||||
| chr15:66432959 | A | AGTGTGTG others(7): Show |
21 | a0001c0001t0001g0002 a0001c0001t0001g0116 a0001c0001t0001g0130 others(18): Show |
21 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.81-2039_81-2026dup others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | ||||||
| chr15:66432959 | A | AGTGTGTG others(9): Show |
18 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0126 others(15): Show |
18 | HG00140.hp1 HG00609.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.81-2041_81-2026dup others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | ||||||
| chr15:66432959 | A | AGTGTGTG others(11): Show |
8 | a0001c0001t0001g0115 a0001c0001t0001g0144 a0001c0001t0001g0286 others(5): Show |
8 | HG00423.hp2 HG00438.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-2043_81-2026dup others(18): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | ||||||
| chr15:66432959 | A | AGTGTGTG others(13): Show |
2 | a0001c0001t0001g0304 a0001c0001t0003g0171 |
2 | HG01071.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.81-2045_81-2026dup others(20): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | ||||||
| chr15:66432959 | A | AGTGTGTG others(21): Show |
1 | a0001c0001t0001g0046 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.81-2053_81-2026dup others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | ||||||
| chr15:66432959 | A | ATGTGTGT others(8): Show |
1 | a0001c0001t0003g0244 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.81-2068_81-2067ins others(15): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432959 | |||||||
| chr15:66432959 | AGT | A | 5 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0127 others(2): Show |
5 | HG00609.hp2 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-2027_81-2026del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | ||||||
| chr15:66432959 | AGTGTGT | A | 5 | a0001c0001t0001g0124 a0001c0001t0001g0344 a0001c0001t0002g0113 others(2): Show |
5 | HG01884.hp2 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-2031_81-2026del others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | ||||||
| chr15:66432959 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0011g0269 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.81-2037_81-2026del others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | ||||||
| chr15:66433007 | G | A | 37 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(34): Show |
37 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.81-2020G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433007 | |||||||
| chr15:66433023 | T | C | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.81-2004T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433023 | |||||||
| chr15:66433066 | C | G | 1 | a0001c0001t0001g0355 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.81-1961C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433066 | |||||||
| chr15:66433217 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-1810T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433217 | |||||||
| chr15:66433277 | C | T | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.81-1750C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433277 | |||||||
| chr15:66433412 | C | T | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81-1615C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433412 | |||||||
| chr15:66433558 | T | C | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.81-1469T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433558 | |||||||
| chr15:66433619 | T | G | 1 | a0001c0001t0001g0355 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.81-1408T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433619 | |||||||
| chr15:66433676 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(78): Show |
82 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.81-1351A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433676 | |||||||
| chr15:66433686 | C | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(78): Show |
82 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.81-1341C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433686 | |||||||
| chr15:66433740 | A | G | 3 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0159 |
3 | HG00280.hp1 HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.81-1287A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433740 | |||||||
| chr15:66433767 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-1260T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433767 | |||||||
| chr15:66433783 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.81-1244A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433783 | |||||||
| chr15:66433809 | G | A | 2 | a0001c0001t0001g0300 a0001c0001t0001g0303 |
2 | NA18989.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.81-1218G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433809 | |||||||
| chr15:66433913 | C | T | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.81-1114C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433913 | |||||||
| chr15:66433990 | C | T | 3 | a0001c0001t0001g0327 a0001c0001t0001g0329 a0001c0001t0001g0330 |
3 | HG02257.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.81-1037C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433990 | |||||||
| chr15:66434027 | A | G | 30 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0341 others(27): Show |
30 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-1000A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434027 | |||||||
| chr15:66434031 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(46): Show |
50 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.81-996C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434031 | |||||||
| chr15:66434064 | A | C | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-963A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434064 | |||||||
| chr15:66434179 | T | C | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.81-848T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434179 | |||||||
| chr15:66434370 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.81-657A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434370 | |||||||
| chr15:66434398 | C | T | 1 | a0001c0001t0001g0365 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.81-629C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434398 | |||||||
| chr15:66434472 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-555G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434472 | |||||||
| chr15:66434569 | G | A | 47 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(44): Show |
47 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.81-458G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434569 | |||||||
| chr15:66434987 | C | G | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.81-40C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434987 | |||||||
| chr15:66435259 | G | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(78): Show |
82 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.291+22G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435259 | |||||||
| chr15:66435351 | A | AT | 12 | a0001c0001t0001g0031 a0001c0001t0001g0142 a0001c0001t0001g0152 others(9): Show |
12 | HG01069.hp2 HG01256.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.291+129dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 66435351 | ||||||
| chr15:66435351 | A | ATT | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(285): Show |
289 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(286): Show |
intron_variant | MODIFIER | c.291+128_291+129dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 66435351 | ||||||
| chr15:66435351 | A | ATTT | 61 | a0001c0001t0001g0307 a0001c0001t0002g0061 a0001c0001t0002g0070 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(58): Show |
intron_variant | MODIFIER | c.291+127_291+129dup others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 66435351 | ||||||
| chr15:66435419 | G | A | 3 | a0001c0001t0001g0327 a0001c0001t0001g0329 a0001c0001t0001g0330 |
3 | HG02257.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.291+182G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435419 | |||||||
| chr15:66435433 | C | G | 1 | a0001c0001t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.291+196C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435433 | |||||||
| chr15:66435436 | C | T | 40 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(37): Show |
40 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.291+199C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435436 | |||||||
| chr15:66435487 | G | A | 2 | a0001c0001t0002g0086 a0001c0001t0002g0096 |
2 | NA19002.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.291+250G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435487 | |||||||
| chr15:66435558 | C | A | 1 | a0001c0001t0002g0100 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.291+321C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435558 | |||||||
| chr15:66435617 | T | C | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.291+380T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435617 | |||||||
| chr15:66435705 | A | G | 1 | a0001c0001t0003g0211 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.291+468A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435705 | |||||||
| chr15:66435931 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(77): Show |
81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.291+694C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435931 | |||||||
| chr15:66435972 | A | G | 51 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(48): Show |
51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.291+735A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435972 | |||||||
| chr15:66436048 | G | C | 1 | a0001c0001t0001g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.292-698G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66436048 | |||||||
| chr15:66436613 | A | C | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-133A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66436613 | |||||||
| chr15:66436912 | C | T | 10 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0159 others(7): Show |
10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.438+20C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66436912 | |||||||
| chr15:66437084 | C | T | 10 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0159 others(7): Show |
10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.438+192C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437084 | |||||||
| chr15:66437095 | T | C | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.438+203T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437095 | |||||||
| chr15:66437231 | G | A | 4 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(1): Show |
4 | HG00673.hp2 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+339G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437231 | |||||||
| chr15:66437295 | G | A | 2 | a0001c0001t0001g0358 a0001c0001t0001g0359 |
2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.438+403G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437295 | |||||||
| chr15:66437539 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.438+647G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437539 | |||||||
| chr15:66437589 | T | C | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.438+697T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437589 | |||||||
| chr15:66437638 | C | T | 4 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0181 others(1): Show |
4 | HG00140.hp1 HG01071.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+746C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437638 | |||||||
| chr15:66437773 | T | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(308): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.438+881T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437773 | |||||||
| chr15:66437844 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.438+952G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437844 | |||||||
| chr15:66437933 | G | T | 1 | a0001c0001t0014g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.438+1041G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437933 | |||||||
| chr15:66437969 | C | T | 51 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(48): Show |
51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.438+1077C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437969 | |||||||
| chr15:66437973 | G | C | 4 | a0001c0001t0001g0224 a0001c0001t0002g0113 a0001c0001t0002g0114 others(1): Show |
4 | HG02109.hp1 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+1081G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437973 | |||||||
| chr15:66437998 | A | T | 1 | a0001c0001t0014g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.438+1106A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437998 | |||||||
| chr15:66438019 | C | CT | 120 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.438+1143dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66438019 | ||||||
| chr15:66438019 | CT | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0102 others(7): Show |
10 | HG01169.hp2 HG01256.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.438+1143delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66438019 | ||||||
| chr15:66438035 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.438+1143T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438035 | |||||||
| chr15:66438159 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.438+1267T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438159 | |||||||
| chr15:66438235 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.438+1343C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438235 | |||||||
| chr15:66438290 | T | C | 6 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG02486.hp2 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.438+1398T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438290 | |||||||
| chr15:66438338 | C | T | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.438+1446C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438338 | |||||||
| chr15:66438362 | C | T | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.438+1470C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438362 | |||||||
| chr15:66438442 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.438+1550T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438442 | |||||||
| chr15:66438443 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.438+1551T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438443 | |||||||
| chr15:66438628 | A | C | 1 | a0001c0001t0006g0003 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.438+1736A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438628 | |||||||
| chr15:66438654 | G | GT | 16 | a0001c0001t0001g0016 a0001c0001t0001g0119 a0001c0001t0001g0120 others(13): Show |
16 | HG00733.hp1 HG01257.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.438+1767dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66438654 | ||||||
| chr15:66438707 | A | C | 51 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(48): Show |
51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.438+1815A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438707 | |||||||
| chr15:66438947 | G | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(109): Show |
113 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.438+2055G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438947 | |||||||
| chr15:66438987 | T | C | 6 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG02486.hp2 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.438+2095T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438987 | |||||||
| chr15:66438990 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.438+2098G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438990 | |||||||
| chr15:66438994 | A | C | 3 | a0001c0001t0001g0327 a0001c0001t0001g0329 a0001c0001t0001g0330 |
3 | HG02257.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.438+2102A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438994 | |||||||
| chr15:66439031 | A | T | 1 | a0001c0001t0001g0260 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.438+2139A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439031 | |||||||
| chr15:66439152 | A | G | 359 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(356): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.438+2260A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439152 | |||||||
| chr15:66439275 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.438+2383C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439275 | |||||||
| chr15:66439370 | A | G | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(359): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.438+2478A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439370 | |||||||
| chr15:66439460 | C | A | 31 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(28): Show |
31 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.438+2568C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439460 | |||||||
| chr15:66439538 | G | A | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.438+2646G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439538 | |||||||
| chr15:66439626 | C | T | 1 | a0001c0001t0003g0244 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.438+2734C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439626 | |||||||
| chr15:66439661 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0232 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.438+2769G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439661 | |||||||
| chr15:66439891 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.438+2999C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439891 | |||||||
| chr15:66439935 | C | CA | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(119): Show |
123 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.438+3061dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66439935 | ||||||
| chr15:66439935 | CA | C | 50 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0102 others(47): Show |
50 | HG00673.hp2 HG00733.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.438+3061delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66439935 | ||||||
| chr15:66440042 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.438+3150A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440042 | |||||||
| chr15:66440092 | TTTTG | T | 40 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(37): Show |
40 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.439-3176_439-3173d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66440092 | ||||||
| chr15:66440114 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.439-3166C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440114 | |||||||
| chr15:66440153 | G | A | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.439-3127G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440153 | |||||||
| chr15:66440278 | A | C | 1 | a0001c0001t0003g0194 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.439-3002A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440278 | |||||||
| chr15:66440394 | G | C | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.439-2886G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440394 | |||||||
| chr15:66440569 | A | G | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.439-2711A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440569 | |||||||
| chr15:66440776 | T | C | 3 | a0001c0001t0001g0273 a0001c0001t0001g0319 a0001c0001t0001g0337 |
3 | HG02451.hp1 HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.439-2504T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440776 | |||||||
| chr15:66440913 | C | G | 1 | a0001c0001t0001g0338 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.439-2367C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440913 | |||||||
| chr15:66440988 | G | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.439-2292G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440988 | |||||||
| chr15:66441067 | G | GTCC | 4 | a0001c0001t0001g0261 a0001c0001t0001g0270 a0001c0001t0001g0307 others(1): Show |
4 | NA18952.hp1 NA18993.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.439-2209_439-2207d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66441067 | ||||||
| chr15:66441189 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0253 |
2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.439-2091C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441189 | |||||||
| chr15:66441300 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.439-1980C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441300 | |||||||
| chr15:66441324 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0253 |
2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.439-1956C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441324 | |||||||
| chr15:66441334 | A | G | 1 | a0001c0001t0003g0194 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.439-1946A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441334 | |||||||
| chr15:66441410 | C | T | 60 | a0001c0001t0001g0213 a0001c0001t0002g0012 a0001c0001t0002g0048 others(57): Show |
60 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.439-1870C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441410 | |||||||
| chr15:66441550 | G | A | 8 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0159 others(5): Show |
8 | HG00280.hp1 HG00438.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.439-1730G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441550 | |||||||
| chr15:66441563 | C | T | 1 | a0001c0001t0012g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.439-1717C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441563 | |||||||
| chr15:66441685 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.439-1595A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441685 | |||||||
| chr15:66441747 | A | T | 1 | a0001c0001t0001g0220 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.439-1533A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441747 | |||||||
| chr15:66441752 | C | CA | 6 | a0001c0001t0001g0011 a0001c0001t0001g0221 a0001c0001t0001g0326 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.439-1514dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66441752 | ||||||
| chr15:66441752 | CA | C | 11 | a0001c0001t0001g0249 a0001c0001t0001g0260 a0001c0001t0003g0168 others(8): Show |
11 | HG00140.hp1 HG00280.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.439-1514delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66441752 | ||||||
| chr15:66441764 | A | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-1516A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441764 | |||||||
| chr15:66441767 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.439-1513C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441767 | |||||||
| chr15:66442308 | T | C | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.439-972T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66442308 | |||||||
| chr15:66442380 | C | A | 38 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(35): Show |
38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.439-900C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66442380 | |||||||
| chr15:66442547 | G | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-733G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66442547 | |||||||
| chr15:66442675 | G | A | 2 | a0001c0001t0007g0056 a0001c0001t0007g0057 |
2 | HG01255.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.439-605G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66442675 | |||||||
| chr15:66442736 | A | G | 3 | a0001c0001t0002g0094 a0001c0001t0003g0178 a0001c0001t0003g0179 |
3 | HG01884.hp1 HG03490.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.439-544A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66442736 | |||||||
| chr15:66442886 | G | A | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.439-394G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66442886 | |||||||
| chr15:66443082 | A | AT | 173 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.439-175dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66443082 | ||||||
| chr15:66443082 | A | ATT | 88 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(85): Show |
88 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.439-176_439-175dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66443082 | ||||||
| chr15:66443082 | A | ATTT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0125 a0001c0001t0001g0156 others(12): Show |
16 | HG00544.hp1 HG01109.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.439-177_439-175dup others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66443082 | ||||||
| chr15:66443082 | A | ATTTT | 6 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0132 others(3): Show |
6 | HG00609.hp2 HG01943.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.439-178_439-175dup others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66443082 | ||||||
| chr15:66443082 | A | ATTTTT | 20 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(17): Show |
20 | HG00733.hp1 HG01257.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.439-179_439-175dup others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66443082 | ||||||
| chr15:66443082 | AT | A | 10 | a0001c0001t0001g0326 a0001c0001t0001g0350 a0001c0001t0006g0003 others(7): Show |
10 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.439-175delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66443082 | ||||||
| chr15:66443112 | G | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.439-168G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66443112 | |||||||
| chr15:66443185 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.439-95C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66443185 | |||||||
| chr15:66443213 | C | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(308): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.439-67C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66443213 | |||||||
| chr15:66443385 | A | G | 1 | a0001c0001t0001g0363 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.516+28A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66443385 | |||||||
| chr15:66443548 | G | A | 48 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(45): Show |
48 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.516+191G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66443548 | |||||||
| chr15:66443587 | C | CAG | 359 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(356): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.516+230_516+231ins others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66443587 | |||||||
| chr15:66443965 | C | T | 41 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(38): Show |
41 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.516+608C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66443965 | |||||||
| chr15:66444035 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.517-621C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444035 | |||||||
| chr15:66444074 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.517-582A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444074 | |||||||
| chr15:66444162 | C | T | 38 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(35): Show |
38 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.517-494C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444162 | |||||||
| chr15:66444273 | C | T | 1 | a0001c0001t0002g0012 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.517-383C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444273 | |||||||
| chr15:66444345 | C | A | 38 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(35): Show |
38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.517-311C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444345 | |||||||
| chr15:66444402 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.517-254G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444402 | |||||||
| chr15:66444403 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(109): Show |
113 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.517-253C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444403 | |||||||
| chr15:66444410 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.517-246G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444410 | |||||||
| chr15:66444426 | A | C | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.517-230A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444426 | |||||||
| chr15:66444472 | G | T | 1 | a0001c0001t0001g0046 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517-184G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444472 | |||||||
| chr15:66444517 | G | T | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.517-139G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444517 | |||||||
| chr15:66444795 | C | T | 6 | a0001c0001t0003g0167 a0001c0001t0003g0201 a0001c0001t0003g0204 others(3): Show |
6 | HG00621.hp2 HG02155.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.568+88C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66444795 | |||||||
| chr15:66444863 | G | A | 1 | a0001c0001t0005g0239 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.568+156G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66444863 | |||||||
| chr15:66444905 | C | T | 1 | a0001c0004t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.568+198C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66444905 | |||||||
| chr15:66445145 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+438A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445145 | |||||||
| chr15:66445148 | G | T | 38 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(35): Show |
38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.568+441G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445148 | |||||||
| chr15:66445157 | T | TG | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(153): Show |
157 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.568+457dupG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66445157 | ||||||
| chr15:66445246 | G | A | 1 | a0001c0001t0001g0339 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.568+539G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445246 | |||||||
| chr15:66445352 | G | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.568+645G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445352 | |||||||
| chr15:66445370 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+663T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445370 | |||||||
| chr15:66445408 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.568+701G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445408 | |||||||
| chr15:66445422 | A | G | 3 | a0001c0001t0003g0174 a0001c0001t0003g0199 a0001c0001t0003g0200 |
3 | HG02572.hp1 NA18906.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.568+715A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445422 | |||||||
| chr15:66445735 | G | T | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.568+1028G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445735 | |||||||
| chr15:66445877 | T | A | 3 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0084 |
3 | NA18954.hp2 NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.568+1170T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445877 | |||||||
| chr15:66446031 | C | T | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.568+1324C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446031 | |||||||
| chr15:66446081 | C | T | 1 | a0001c0001t0005g0242 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.568+1374C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446081 | |||||||
| chr15:66446086 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.568+1379G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446086 | |||||||
| chr15:66446155 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.568+1448G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446155 | |||||||
| chr15:66446204 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG01261.hp2 HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.568+1497G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446204 | |||||||
| chr15:66446257 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.568+1550G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446257 | |||||||
| chr15:66446382 | C | T | 1 | a0001c0001t0001g0362 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.568+1675C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446382 | |||||||
| chr15:66446440 | C | CA | 8 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0136 others(5): Show |
8 | HG01891.hp2 HG02970.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+1748dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66446440 | ||||||
| chr15:66446515 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.568+1808C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446515 | |||||||
| chr15:66446528 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.568+1821C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446528 | |||||||
| chr15:66446637 | A | G | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | NA18946.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.568+1930A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446637 | |||||||
| chr15:66446656 | A | G | 1 | a0001c0001t0011g0269 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.568+1949A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446656 | |||||||
| chr15:66446712 | C | CAG | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.568+2005_568+2006i others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446712 | |||||||
| chr15:66446748 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+2041G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446748 | |||||||
| chr15:66446780 | A | AT | 41 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(38): Show |
41 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.568+2074dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66446780 | ||||||
| chr15:66446953 | A | G | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.568+2246A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446953 | |||||||
| chr15:66447074 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.568+2367C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447074 | |||||||
| chr15:66447195 | C | A | 1 | a0001c0001t0002g0071 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.568+2488C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447195 | |||||||
| chr15:66447332 | A | G | 38 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(35): Show |
38 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.568+2625A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447332 | |||||||
| chr15:66447426 | A | G | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.568+2719A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447426 | |||||||
| chr15:66447501 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.568+2794G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447501 | |||||||
| chr15:66447550 | G | A | 29 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0341 others(26): Show |
29 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.568+2843G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447550 | |||||||
| chr15:66447554 | G | T | 1 | a0001c0001t0002g0098 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.568+2847G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447554 | |||||||
| chr15:66447555 | G | T | 1 | a0001c0001t0002g0083 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.568+2848G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447555 | |||||||
| chr15:66447592 | T | C | 2 | a0001c0001t0001g0304 a0001c0001t0001g0306 |
2 | HG01952.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.568+2885T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447592 | |||||||
| chr15:66447686 | C | CA | 220 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0111 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.568+2994dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66447686 | ||||||
| chr15:66447686 | C | CAA | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(92): Show |
96 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.568+2993_568+2994d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66447686 | ||||||
| chr15:66447705 | T | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(78): Show |
82 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.568+2998T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447705 | |||||||
| chr15:66447839 | G | C | 6 | a0001c0001t0003g0166 a0001c0001t0003g0172 a0001c0001t0003g0188 others(3): Show |
6 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.568+3132G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447839 | |||||||
| chr15:66448085 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.568+3378G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448085 | |||||||
| chr15:66448152 | C | CA | 15 | a0001c0001t0001g0011 a0001c0001t0001g0108 a0001c0001t0001g0144 others(12): Show |
15 | HG00544.hp2 HG00621.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.568+3466dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66448152 | ||||||
| chr15:66448152 | C | CAA | 115 | a0001c0001t0001g0016 a0001c0001t0001g0111 a0001c0001t0001g0112 others(112): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.568+3465_568+3466d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66448152 | ||||||
| chr15:66448152 | C | CAAA | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(76): Show |
80 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.568+3464_568+3466d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66448152 | ||||||
| chr15:66448152 | C | CAAAA | 7 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0001g0270 others(4): Show |
7 | HG01175.hp2 HG01346.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.568+3463_568+3466d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66448152 | ||||||
| chr15:66448157 | A | AC | 48 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(45): Show |
48 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.568+3450_568+3451i others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448157 | |||||||
| chr15:66448162 | A | AAG | 50 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(47): Show |
50 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.568+3456_568+3457i others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66448162 | ||||||
| chr15:66448162 | A | C | 48 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(45): Show |
48 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.568+3455A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448162 | |||||||
| chr15:66448162 | A | G | 1 | a0001c0001t0003g0184 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.568+3455A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448162 | |||||||
| chr15:66448166 | A | C | 41 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(38): Show |
41 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.568+3459A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448166 | |||||||
| chr15:66448173 | A | C | 2 | a0001c0001t0005g0160 a0001c0001t0005g0161 |
2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.568+3466A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448173 | |||||||
| chr15:66448227 | C | A | 1 | a0001c0001t0003g0164 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.568+3520C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448227 | |||||||
| chr15:66448502 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0045 |
2 | HG00738.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.568+3795A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448502 | |||||||
| chr15:66448663 | T | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0230 |
2 | HG01934.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.568+3956T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448663 | |||||||
| chr15:66448683 | T | C | 1 | a0001c0001t0003g0193 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.568+3976T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448683 | |||||||
| chr15:66448818 | A | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.568+4111A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448818 | |||||||
| chr15:66448831 | C | T | 1 | a0001c0001t0001g0338 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.568+4124C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448831 | |||||||
| chr15:66448872 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.568+4165C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448872 | |||||||
| chr15:66448996 | A | T | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.568+4289A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448996 | |||||||
| chr15:66449003 | C | CA | 150 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0032 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.568+4321dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66449003 | ||||||
| chr15:66449003 | C | CAA | 76 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0038 others(73): Show |
76 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.568+4320_568+4321d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66449003 | ||||||
| chr15:66449003 | C | CAAA | 11 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0216 others(8): Show |
11 | HG00741.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.568+4319_568+4321d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66449003 | ||||||
| chr15:66449003 | CA | C | 9 | a0001c0001t0001g0265 a0001c0001t0006g0003 a0001c0001t0006g0004 others(6): Show |
9 | HG00280.hp2 HG00639.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.568+4321delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66449003 | ||||||
| chr15:66449029 | C | A | 2 | a0001c0001t0002g0055 a0001c0001t0002g0097 |
2 | HG00597.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.568+4322C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449029 | |||||||
| chr15:66449049 | C | G | 51 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(48): Show |
51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.568+4342C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449049 | |||||||
| chr15:66449124 | T | A | 1 | a0001c0001t0001g0301 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.568+4417T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449124 | |||||||
| chr15:66449398 | T | G | 31 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(28): Show |
31 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.568+4691T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449398 | |||||||
| chr15:66449477 | AAAGTGCA others(1): Show |
A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.568+4774_568+4781d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66449477 | ||||||
| chr15:66449618 | C | T | 2 | a0001c0001t0001g0300 a0001c0001t0006g0004 |
2 | HG02602.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.568+4911C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449618 | |||||||
| chr15:66449632 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.568+4925G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449632 | |||||||
| chr15:66449657 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(109): Show |
113 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.568+4950G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449657 | |||||||
| chr15:66449692 | C | T | 55 | a0001c0001t0001g0213 a0001c0001t0002g0012 a0001c0001t0002g0048 others(52): Show |
55 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.568+4985C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449692 | |||||||
| chr15:66449763 | C | T | 3 | a0001c0001t0001g0248 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.568+5056C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449763 | |||||||
| chr15:66450165 | T | A | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(359): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.568+5458T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450165 | |||||||
| chr15:66450186 | C | T | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(359): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.568+5479C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450186 | |||||||
| chr15:66450223 | T | C | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.568+5516T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450223 | |||||||
| chr15:66450228 | C | G | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.568+5521C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450228 | |||||||
| chr15:66450253 | A | G | 359 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(356): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.568+5546A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450253 | |||||||
| chr15:66450264 | A | G | 10 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0159 others(7): Show |
10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.568+5557A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450264 | |||||||
| chr15:66450348 | T | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+5641T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450348 | |||||||
| chr15:66450393 | T | A | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.568+5686T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450393 | |||||||
| chr15:66450394 | C | T | 1 | a0001c0001t0003g0205 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.568+5687C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450394 | |||||||
| chr15:66450395 | G | A | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.568+5688G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450395 | |||||||
| chr15:66450434 | A | G | 4 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.568+5727A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450434 | |||||||
| chr15:66450504 | CAGAG | C | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.568+5800_568+5803d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66450504 | ||||||
| chr15:66450580 | A | G | 54 | a0001c0001t0001g0213 a0001c0001t0002g0012 a0001c0001t0002g0048 others(51): Show |
54 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.568+5873A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450580 | |||||||
| chr15:66450607 | G | T | 41 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(38): Show |
41 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.568+5900G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450607 | |||||||
| chr15:66450695 | G | A | 1 | a0001c0002t0001g0297 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.568+5988G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450695 | |||||||
| chr15:66450810 | A | G | 2 | a0001c0001t0003g0163 a0001c0001t0003g0180 |
2 | HG01515.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.568+6103A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450810 | |||||||
| chr15:66450874 | AC | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+6169delC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66450874 | ||||||
| chr15:66450985 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.568+6278A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450985 | |||||||
| chr15:66450988 | T | C | 21 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0219 others(18): Show |
21 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.568+6281T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450988 | |||||||
| chr15:66451008 | T | C | 10 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0159 others(7): Show |
10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.568+6301T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451008 | |||||||
| chr15:66451113 | TC | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+6408delC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66451113 | ||||||
| chr15:66451175 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.568+6468A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451175 | |||||||
| chr15:66451226 | G | A | 9 | a0001c0001t0001g0002 a0001c0001t0006g0003 a0001c0001t0006g0004 others(6): Show |
9 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.568+6519G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451226 | |||||||
| chr15:66451306 | C | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+6599C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451306 | |||||||
| chr15:66451379 | G | A | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.568+6672G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451379 | |||||||
| chr15:66451448 | A | AAAAC | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+6744_568+6747d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66451448 | ||||||
| chr15:66451472 | T | C | 359 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(356): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.568+6765T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451472 | |||||||
| chr15:66451617 | A | C | 1 | a0001c0001t0002g0062 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.568+6910A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451617 | |||||||
| chr15:66451829 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(77): Show |
81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.568+7122C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451829 | |||||||
| chr15:66451884 | A | G | 38 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(35): Show |
38 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.568+7177A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451884 | |||||||
| chr15:66451948 | T | C | 2 | a0001c0001t0001g0223 a0001c0001t0001g0233 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.568+7241T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451948 | |||||||
| chr15:66451963 | A | C | 21 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0219 others(18): Show |
21 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.568+7256A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451963 | |||||||
| chr15:66451975 | A | C | 1 | a0001c0001t0001g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.568+7268A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451975 | |||||||
| chr15:66452002 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(77): Show |
81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.568+7295T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452002 | |||||||
| chr15:66452031 | G | A | 11 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(8): Show |
11 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.568+7324G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452031 | |||||||
| chr15:66452151 | G | C | 10 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0159 others(7): Show |
10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.568+7444G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452151 | |||||||
| chr15:66452166 | T | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.568+7459T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452166 | |||||||
| chr15:66452170 | G | T | 1 | a0001c0001t0004g0021 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.568+7463G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452170 | |||||||
| chr15:66452195 | C | T | 1 | a0001c0001t0001g0362 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.568+7488C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452195 | |||||||
| chr15:66452210 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(109): Show |
113 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.568+7503C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452210 | |||||||
| chr15:66452226 | A | C | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.568+7519A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452226 | |||||||
| chr15:66452265 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+7558C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452265 | |||||||
| chr15:66452294 | A | AAAG | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+7589_568+7590i others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66452294 | ||||||
| chr15:66452300 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+7593A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452300 | |||||||
| chr15:66452301 | A | AAAAG | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(115): Show |
119 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.568+7596_568+7597i others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66452301 | ||||||
| chr15:66452302 | A | AAAAG | 120 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(117): Show |
120 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.568+7596_568+7597i others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66452302 | ||||||
| chr15:66452302 | A | AAAG | 50 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(47): Show |
50 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.568+7596_568+7597i others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66452302 | ||||||
| chr15:66452303 | A | AAG | 6 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.568+7596_568+7597i others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452303 | |||||||
| chr15:66452304 | G | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(309): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.568+7597G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452304 | |||||||
| chr15:66452304 | G | GAA | 41 | a0001c0001t0001g0011 a0001c0001t0001g0156 a0001c0001t0001g0322 others(38): Show |
41 | HG00733.hp2 HG01109.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.568+7606_568+7607d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66452304 | ||||||
| chr15:66452349 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.568+7642A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452349 | |||||||
| chr15:66452412 | T | G | 2 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.568+7705T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452412 | |||||||
| chr15:66452435 | C | G | 359 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(356): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.568+7728C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452435 | |||||||
| chr15:66452559 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.568+7852T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452559 | |||||||
| chr15:66452673 | G | A | 3 | a0001c0001t0002g0086 a0001c0001t0002g0095 a0001c0001t0002g0096 |
3 | NA18962.hp2 NA19002.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.568+7966G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452673 | |||||||
| chr15:66452682 | G | T | 3 | a0001c0001t0002g0086 a0001c0001t0002g0095 a0001c0001t0002g0096 |
3 | NA18962.hp2 NA19002.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.568+7975G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452682 | |||||||
| chr15:66452755 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.568+8048A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452755 | |||||||
| chr15:66452787 | C | T | 1 | a0001c0001t0006g0007 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.568+8080C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452787 | |||||||
| chr15:66452799 | T | C | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.568+8092T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452799 | |||||||
| chr15:66453174 | C | G | 1 | a0001c0001t0003g0169 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.568+8467C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66453174 | |||||||
| chr15:66453198 | A | T | 1 | a0001c0001t0002g0068 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.568+8491A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66453198 | |||||||
| chr15:66453390 | A | C | 3 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0159 |
3 | HG00280.hp1 HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.568+8683A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66453390 | |||||||
| chr15:66453552 | G | A | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(359): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.568+8845G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66453552 | |||||||
| chr15:66453591 | G | C | 30 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0214 others(27): Show |
30 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.568+8884G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66453591 | |||||||
| chr15:66453855 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.568+9148G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66453855 | |||||||
| chr15:66454122 | G | A | 48 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(45): Show |
48 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.568+9415G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454122 | |||||||
| chr15:66454132 | G | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.568+9425G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454132 | |||||||
| chr15:66454218 | C | A | 3 | a0001c0001t0001g0309 a0001c0001t0001g0313 a0001c0001t0001g0314 |
3 | HG02027.hp1 NA19010.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.568+9511C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454218 | |||||||
| chr15:66454296 | T | TC | 48 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(45): Show |
48 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.568+9591dupC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66454296 | ||||||
| chr15:66454553 | C | T | 31 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(28): Show |
31 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.568+9846C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454553 | |||||||
| chr15:66454554 | C | T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.568+9847C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454554 | |||||||
| chr15:66454750 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.568+10043C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454750 | |||||||
| chr15:66454815 | G | A | 1 | a0001c0001t0003g0168 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.568+10108G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454815 | |||||||
| chr15:66454983 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(77): Show |
81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.568+10276T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454983 | |||||||
| chr15:66455068 | C | T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.568+10361C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455068 | |||||||
| chr15:66455194 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.568+10487C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455194 | |||||||
| chr15:66455243 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.568+10536A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455243 | |||||||
| chr15:66455560 | TC | T | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.568+10855delC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66455560 | ||||||
| chr15:66455571 | G | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(109): Show |
113 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.568+10864G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455571 | |||||||
| chr15:66455665 | A | G | 1 | a0001c0001t0012g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.568+10958A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455665 | |||||||
| chr15:66455763 | G | A | 1 | a0001c0001t0001g0364 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.568+11056G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455763 | |||||||
| chr15:66455869 | T | G | 1 | a0001c0001t0001g0279 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.568+11162T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455869 | |||||||
| chr15:66455874 | T | A | 20 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0219 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.568+11167T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455874 | |||||||
| chr15:66455875 | C | A | 20 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0219 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.568+11168C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455875 | |||||||
| chr15:66456068 | C | T | 1 | a0001c0001t0006g0003 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.568+11361C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66456068 | |||||||
| chr15:66456330 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0262 |
2 | HG02559.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.568+11623C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66456330 | |||||||
| chr15:66456568 | C | T | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG00609.hp2 NA18947.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.568+11861C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66456568 | |||||||
| chr15:66456606 | A | G | 60 | a0001c0001t0001g0213 a0001c0001t0002g0012 a0001c0001t0002g0048 others(57): Show |
60 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.568+11899A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66456606 | |||||||
| chr15:66456717 | A | C | 11 | a0001c0001t0001g0350 a0001c0001t0001g0352 a0001c0001t0001g0356 others(8): Show |
11 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.568+12010A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66456717 | |||||||
| chr15:66456921 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.568+12214C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66456921 | |||||||
| chr15:66456933 | C | G | 1 | a0001c0001t0012g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.568+12226C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66456933 | |||||||
| chr15:66457115 | TTTA | T | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.568+12417_568+1241 others(7): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66457115 | ||||||
| chr15:66457187 | C | T | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(307): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.568+12480C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457187 | |||||||
| chr15:66457276 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.568+12569G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457276 | |||||||
| chr15:66457292 | G | A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(307): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.568+12585G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457292 | |||||||
| chr15:66457308 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(77): Show |
81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.568+12601C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457308 | |||||||
| chr15:66457369 | C | T | 2 | a0001c0001t0003g0188 a0001c0001t0003g0189 |
2 | HG00642.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.568+12662C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457369 | |||||||
| chr15:66457579 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(77): Show |
81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.568+12872C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457579 | |||||||
| chr15:66457727 | C | A | 2 | a0001c0001t0003g0164 a0001c0001t0003g0173 |
2 | HG03491.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.568+13020C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457727 | |||||||
| chr15:66457732 | C | T | 50 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(47): Show |
50 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.568+13025C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457732 | |||||||
| chr15:66457756 | G | A | 90 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0213 others(87): Show |
90 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.568+13049G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457756 | |||||||
| chr15:66457791 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+13084G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457791 | |||||||
| chr15:66457835 | C | T | 26 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0214 others(23): Show |
26 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.568+13128C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457835 | |||||||
| chr15:66457911 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.568+13204C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457911 | |||||||
| chr15:66457963 | G | GA | 13 | a0001c0001t0001g0213 a0001c0001t0001g0272 a0001c0001t0001g0317 others(10): Show |
13 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.568+13271dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66457963 | ||||||
| chr15:66458186 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+13479A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458186 | |||||||
| chr15:66458277 | A | C | 90 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0213 others(87): Show |
90 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.568+13570A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458277 | |||||||
| chr15:66458309 | G | A | 2 | a0001c0001t0003g0186 a0001c0001t0003g0210 |
2 | HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.568+13602G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458309 | |||||||
| chr15:66458313 | C | T | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(307): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.568+13606C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458313 | |||||||
| chr15:66458351 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | HG02970.hp2 HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.568+13644G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458351 | |||||||
| chr15:66458712 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.568+14005G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458712 | |||||||
| chr15:66458730 | A | C | 1 | a0001c0001t0002g0051 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.568+14023A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458730 | |||||||
| chr15:66458914 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(77): Show |
81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.568+14207T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458914 | |||||||
| chr15:66459130 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.568+14423C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459130 | |||||||
| chr15:66459205 | T | C | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(359): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.568+14498T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459205 | |||||||
| chr15:66459309 | C | CA | 49 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0115 others(46): Show |
49 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.568+14619dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66459309 | ||||||
| chr15:66459309 | CA | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(290): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.568+14619delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66459309 | ||||||
| chr15:66459383 | A | G | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.568+14676A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459383 | |||||||
| chr15:66459441 | A | T | 2 | a0001c0001t0005g0160 a0001c0001t0005g0161 |
2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.568+14734A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459441 | |||||||
| chr15:66459541 | A | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+14834A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459541 | |||||||
| chr15:66459551 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.568+14844G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459551 | |||||||
| chr15:66459616 | T | TG | 56 | a0001c0001t0001g0224 a0001c0001t0002g0012 a0001c0001t0002g0048 others(53): Show |
56 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.568+14909_568+1491 others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459616 | |||||||
| chr15:66459616 | T | TGA | 3 | a0001c0001t0002g0067 a0001c0001t0002g0077 a0001c0001t0008g0073 |
3 | HG02886.hp1 NA18949.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.568+14909_568+1491 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459616 | |||||||
| chr15:66459617 | C | A | 59 | a0001c0001t0001g0224 a0001c0001t0002g0012 a0001c0001t0002g0048 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.568+14910C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459617 | |||||||
| chr15:66459617 | C | CA | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(220): Show |
224 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.568+14925dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66459617 | ||||||
| chr15:66459617 | C | CAA | 53 | a0001c0001t0001g0320 a0001c0001t0001g0322 a0001c0001t0001g0323 others(50): Show |
53 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.568+14924_568+1492 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66459617 | ||||||
| chr15:66459617 | C | G | 5 | a0001c0001t0001g0213 a0001c0001t0002g0052 a0001c0001t0002g0053 others(2): Show |
5 | HG02280.hp1 NA18954.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.568+14910C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459617 | |||||||
| chr15:66459632 | A | AT | 10 | a0001c0001t0003g0206 a0001c0001t0005g0157 a0001c0001t0005g0158 others(7): Show |
10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.568+14933dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66459632 | ||||||
| chr15:66459632 | A | T | 1 | a0001c0001t0005g0241 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.568+14925A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459632 | |||||||
| chr15:66459633 | T | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0277 |
2 | HG02683.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.568+14926T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459633 | |||||||
| chr15:66459917 | C | T | 2 | a0001c0001t0002g0061 a0001c0001t0002g0070 |
2 | HG00099.hp2 HG00140.hp2 |
intron_variant | MODIFIER | c.568+15210C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459917 | |||||||
| chr15:66460054 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.568+15347T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460054 | |||||||
| chr15:66460068 | G | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+15361G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460068 | |||||||
| chr15:66460155 | G | A | 1 | a0001c0001t0003g0211 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.568+15448G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460155 | |||||||
| chr15:66460187 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.568+15480G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460187 | |||||||
| chr15:66460326 | G | A | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.568+15619G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460326 | |||||||
| chr15:66460452 | A | G | 1 | a0001c0001t0001g0327 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.568+15745A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460452 | |||||||
| chr15:66460487 | A | T | 1 | a0001c0001t0002g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.568+15780A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460487 | |||||||
| chr15:66460580 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.568+15873G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460580 | |||||||
| chr15:66460696 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.568+15989G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460696 | |||||||
| chr15:66460830 | G | C | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.568+16123G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460830 | |||||||
| chr15:66460872 | G | C | 1 | a0001c0001t0001g0354 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.568+16165G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460872 | |||||||
| chr15:66460983 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0126 |
2 | NA18949.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.568+16276C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460983 | |||||||
| chr15:66461163 | T | C | 1 | a0001c0002t0001g0297 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.568+16456T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461163 | |||||||
| chr15:66461476 | C | CTAAA | 134 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0032 others(131): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.568+16805_568+1680 others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66461476 | ||||||
| chr15:66461476 | C | CTAAATAA others(1): Show |
7 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0003g0195 others(4): Show |
7 | HG00099.hp1 HG01433.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.568+16801_568+1680 others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66461476 | ||||||
| chr15:66461476 | CTAAA | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(145): Show |
149 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.568+16805_568+1680 others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66461476 | ||||||
| chr15:66461476 | CTAAATAA others(1): Show |
C | 13 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(10): Show |
13 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.568+16801_568+1680 others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66461476 | ||||||
| chr15:66461516 | T | A | 1 | a0001c0001t0003g0163 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.568+16809T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461516 | |||||||
| chr15:66461517 | A | T | 1 | a0001c0001t0003g0163 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.568+16810A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461517 | |||||||
| chr15:66461581 | A | G | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.568+16874A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461581 | |||||||
| chr15:66461765 | C | T | 2 | a0001c0001t0001g0343 a0001c0001t0001g0344 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.568+17058C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461765 | |||||||
| chr15:66461791 | T | C | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.568+17084T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461791 | |||||||
| chr15:66461816 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.568+17109G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461816 | |||||||
| chr15:66461872 | A | G | 2 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.568+17165A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461872 | |||||||
| chr15:66462216 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.568+17509T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462216 | |||||||
| chr15:66462314 | A | G | 1 | a0001c0001t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.568+17607A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462314 | |||||||
| chr15:66462359 | G | C | 5 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(2): Show |
5 | HG00438.hp2 NA18963.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.568+17652G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462359 | |||||||
| chr15:66462399 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.568+17692C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462399 | |||||||
| chr15:66462422 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.568+17715G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462422 | |||||||
| chr15:66462446 | G | A | 1 | a0001c0006t0001g0353 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.568+17739G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462446 | |||||||
| chr15:66462496 | C | CA | 117 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0101 others(114): Show |
117 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.568+17809dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66462496 | ||||||
| chr15:66462496 | C | CAA | 35 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0156 others(32): Show |
35 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.568+17808_568+1780 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66462496 | ||||||
| chr15:66462496 | CA | C | 7 | a0001c0001t0001g0143 a0001c0001t0001g0271 a0001c0001t0001g0292 others(4): Show |
7 | HG00738.hp1 HG01516.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.568+17809delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66462496 | ||||||
| chr15:66462593 | A | G | 2 | a0001c0001t0004g0023 a0001c0001t0004g0042 |
2 | NA18977.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.568+17886A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462593 | |||||||
| chr15:66462603 | G | GA | 29 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(26): Show |
29 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.568+17907dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66462603 | ||||||
| chr15:66462603 | G | GAAAA | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+17904_568+1790 others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66462603 | ||||||
| chr15:66462603 | GA | G | 107 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0102 others(104): Show |
107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.568+17907delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66462603 | ||||||
| chr15:66462722 | G | C | 1 | a0001c0001t0004g0043 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.568+18015G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462722 | |||||||
| chr15:66462884 | C | T | 3 | a0001c0001t0002g0058 a0001c0001t0002g0080 a0001c0001t0002g0081 |
3 | NA18972.hp1 NA19057.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.568+18177C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462884 | |||||||
| chr15:66462896 | G | A | 4 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.568+18189G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462896 | |||||||
| chr15:66462907 | G | A | 51 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0102 others(48): Show |
51 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.568+18200G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462907 | |||||||
| chr15:66463115 | T | C | 3 | a0001c0001t0001g0309 a0001c0001t0001g0313 a0001c0001t0001g0314 |
3 | HG02027.hp1 NA19010.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.568+18408T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463115 | |||||||
| chr15:66463184 | T | G | 31 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(28): Show |
31 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.568+18477T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463184 | |||||||
| chr15:66463277 | C | G | 1 | a0001c0001t0001g0319 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.569-18478C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463277 | |||||||
| chr15:66463495 | T | A | 1 | a0001c0001t0003g0194 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.569-18260T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463495 | |||||||
| chr15:66463585 | C | T | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.569-18170C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463585 | |||||||
| chr15:66463597 | G | A | 25 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(22): Show |
25 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.569-18158G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463597 | |||||||
| chr15:66463627 | C | T | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.569-18128C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463627 | |||||||
| chr15:66463635 | A | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.569-18120A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463635 | |||||||
| chr15:66463830 | T | C | 1 | a0001c0001t0006g0010 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.569-17925T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463830 | |||||||
| chr15:66463832 | T | C | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.569-17923T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463832 | |||||||
| chr15:66464132 | G | A | 51 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0102 others(48): Show |
51 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.569-17623G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464132 | |||||||
| chr15:66464181 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(78): Show |
82 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.569-17574C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464181 | |||||||
| chr15:66464501 | G | GGAAAA | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-17249_569-1724 others(9): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66464501 | ||||||
| chr15:66464503 | A | G | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-17252A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464503 | |||||||
| chr15:66464559 | T | C | 1 | a0001c0001t0002g0148 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.569-17196T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464559 | |||||||
| chr15:66464585 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.569-17170C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464585 | |||||||
| chr15:66464587 | T | C | 332 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(329): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.569-17168T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464587 | |||||||
| chr15:66464650 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(110): Show |
114 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.569-17105T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464650 | |||||||
| chr15:66464672 | T | A | 3 | a0001c0001t0001g0366 a0001c0001t0001g0367 a0001c0001t0001g0369 |
3 | HG02559.hp2 HG02895.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.569-17083T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464672 | |||||||
| chr15:66464674 | C | T | 50 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(47): Show |
50 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.569-17081C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464674 | |||||||
| chr15:66464675 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.569-17080G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464675 | |||||||
| chr15:66464765 | G | T | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.569-16990G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464765 | |||||||
| chr15:66464770 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-16985C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464770 | |||||||
| chr15:66464949 | A | G | 329 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(326): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.569-16806A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464949 | |||||||
| chr15:66464953 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-16802T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464953 | |||||||
| chr15:66465122 | G | A | 41 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(38): Show |
41 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.569-16633G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465122 | |||||||
| chr15:66465123 | G | C | 1 | a0001c0001t0001g0338 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.569-16632G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465123 | |||||||
| chr15:66465202 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.569-16553G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465202 | |||||||
| chr15:66465224 | C | T | 11 | a0001c0001t0003g0206 a0001c0001t0005g0157 a0001c0001t0005g0158 others(8): Show |
11 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.569-16531C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465224 | |||||||
| chr15:66465349 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.569-16406C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465349 | |||||||
| chr15:66465353 | A | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(110): Show |
114 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.569-16402A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465353 | |||||||
| chr15:66465490 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.569-16265C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465490 | |||||||
| chr15:66465623 | T | A | 61 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.569-16132T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465623 | |||||||
| chr15:66465708 | A | C | 1 | a0001c0001t0001g0314 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.569-16047A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465708 | |||||||
| chr15:66465737 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.569-16018G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465737 | |||||||
| chr15:66465829 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-15926G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465829 | |||||||
| chr15:66466045 | C | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-15710C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66466045 | |||||||
| chr15:66466354 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-15401C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66466354 | |||||||
| chr15:66466356 | A | G | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.569-15399A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66466356 | |||||||
| chr15:66466371 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.569-15384G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66466371 | |||||||
| chr15:66466437 | C | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.569-15318C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66466437 | |||||||
| chr15:66466503 | A | T | 1 | a0001c0001t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.569-15252A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66466503 | |||||||
| chr15:66466579 | C | T | 1 | a0001c0001t0002g0055 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.569-15176C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66466579 | |||||||
| chr15:66467094 | G | A | 3 | a0001c0001t0006g0005 a0001c0001t0006g0008 a0001c0001t0006g0009 |
3 | HG01515.hp1 HG01517.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.569-14661G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467094 | |||||||
| chr15:66467181 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.569-14574C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467181 | |||||||
| chr15:66467221 | C | T | 1 | a0001c0001t0002g0058 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.569-14534C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467221 | |||||||
| chr15:66467229 | C | T | 4 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0181 others(1): Show |
4 | HG00140.hp1 HG01071.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-14526C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467229 | |||||||
| chr15:66467266 | A | G | 1 | a0001c0001t0007g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.569-14489A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467266 | |||||||
| chr15:66467361 | G | A | 41 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(38): Show |
41 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.569-14394G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467361 | |||||||
| chr15:66467543 | C | T | 3 | a0001c0001t0001g0259 a0001c0001t0001g0271 a0001c0001t0001g0318 |
3 | HG02895.hp2 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.569-14212C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467543 | |||||||
| chr15:66467647 | G | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.569-14108G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467647 | |||||||
| chr15:66468004 | A | G | 92 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0213 others(89): Show |
92 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.569-13751A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468004 | |||||||
| chr15:66468246 | A | T | 1 | a0001c0001t0001g0365 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.569-13509A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468246 | |||||||
| chr15:66468269 | CT | C | 7 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(4): Show |
7 | HG01257.hp2 HG02615.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.569-13477delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66468269 | ||||||
| chr15:66468271 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.569-13484T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468271 | |||||||
| chr15:66468281 | C | G | 2 | a0001c0001t0001g0338 a0001c0004t0001g0015 |
2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.569-13474C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468281 | |||||||
| chr15:66468291 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.569-13464C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468291 | |||||||
| chr15:66468361 | C | A | 1 | a0001c0001t0001g0295 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.569-13394C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468361 | |||||||
| chr15:66468377 | A | G | 1 | a0001c0001t0003g0166 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.569-13378A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468377 | |||||||
| chr15:66468442 | G | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-13313G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468442 | |||||||
| chr15:66468553 | T | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-13202T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468553 | |||||||
| chr15:66468569 | T | C | 15 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(12): Show |
15 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.569-13186T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468569 | |||||||
| chr15:66468581 | C | T | 1 | a0001c0001t0001g0305 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.569-13174C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468581 | |||||||
| chr15:66468633 | TA | T | 4 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-13114delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66468633 | ||||||
| chr15:66468634 | A | T | 7 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-13121A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468634 | |||||||
| chr15:66468642 | T | A | 62 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(59): Show |
62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.569-13113T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468642 | |||||||
| chr15:66468645 | T | G | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-13110T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468645 | |||||||
| chr15:66468708 | G | A | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.569-13047G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468708 | |||||||
| chr15:66468734 | C | A | 1 | a0001c0001t0003g0205 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.569-13021C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468734 | |||||||
| chr15:66468743 | C | T | 1 | a0001c0001t0005g0160 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.569-13012C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468743 | |||||||
| chr15:66468792 | G | A | 1 | a0001c0001t0001g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.569-12963G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468792 | |||||||
| chr15:66468807 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-12948T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468807 | |||||||
| chr15:66468868 | TTGCAGTG others(17): Show |
T | 64 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(61): Show |
64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.569-12858_569-1283 others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66468868 | ||||||
| chr15:66468903 | TG | T | 37 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(34): Show |
37 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.569-12851delG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468903 | |||||||
| chr15:66468949 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.569-12806G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468949 | |||||||
| chr15:66468953 | C | CA | 47 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(44): Show |
47 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.569-12791dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66468953 | ||||||
| chr15:66469029 | G | T | 1 | a0001c0001t0001g0046 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.569-12726G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469029 | |||||||
| chr15:66469149 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0253 |
2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.569-12606C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469149 | |||||||
| chr15:66469173 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-12582T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469173 | |||||||
| chr15:66469175 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-12580G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469175 | |||||||
| chr15:66469176 | A | T | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-12579A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469176 | |||||||
| chr15:66469179 | C | A | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-12576C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469179 | |||||||
| chr15:66469180 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-12575C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469180 | |||||||
| chr15:66469185 | G | T | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-12570G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469185 | |||||||
| chr15:66469189 | G | T | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-12566G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469189 | |||||||
| chr15:66469472 | C | CT | 52 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0045 others(49): Show |
52 | HG00544.hp2 HG00621.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.569-12256dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | ||||||
| chr15:66469472 | C | CTT | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(126): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.569-12257_569-1225 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | ||||||
| chr15:66469472 | C | CTTT | 40 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(37): Show |
40 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.569-12258_569-1225 others(7): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | ||||||
| chr15:66469472 | C | CTTTTTT | 15 | a0001c0001t0001g0327 a0001c0001t0001g0332 a0001c0001t0001g0341 others(12): Show |
15 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.569-12261_569-1225 others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | ||||||
| chr15:66469472 | C | CTTTTTTT | 11 | a0001c0001t0001g0331 a0001c0001t0001g0343 a0001c0001t0001g0346 others(8): Show |
11 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.569-12262_569-1225 others(11): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | ||||||
| chr15:66469472 | CTT | C | 6 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.569-12257_569-1225 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | ||||||
| chr15:66469472 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0031 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.569-12267_569-1225 others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | ||||||
| chr15:66469472 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0300 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.569-12268_569-1225 others(17): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | ||||||
| chr15:66469535 | G | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-12220G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469535 | |||||||
| chr15:66469557 | C | G | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-12198C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469557 | |||||||
| chr15:66469611 | GAGA | G | 7 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-12136_569-1213 others(7): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469611 | ||||||
| chr15:66469637 | A | G | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG00609.hp2 NA18947.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12118A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469637 | |||||||
| chr15:66469661 | AAAAC | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-12089_569-1208 others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469661 | ||||||
| chr15:66469693 | G | GAC | 8 | a0001c0001t0001g0011 a0001c0001t0001g0333 a0001c0001t0001g0343 others(5): Show |
8 | HG01099.hp2 HG01884.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.569-12032_569-1203 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACAC | 3 | a0001c0001t0001g0325 a0001c0001t0006g0008 a0001c0001t0006g0009 |
3 | HG01515.hp1 HG01517.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.569-12034_569-1203 others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(1): Show |
4 | a0001c0001t0001g0309 a0001c0001t0001g0312 a0001c0001t0001g0313 others(1): Show |
4 | HG00639.hp2 NA18522.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12038_569-1203 others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(3): Show |
47 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(44): Show |
48 | HG00609.hp1 HG00735.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.569-12040_569-1203 others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(5): Show |
26 | a0001c0001t0001g0002 a0001c0001t0001g0046 a0001c0001t0001g0115 others(23): Show |
26 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.569-12042_569-1203 others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(7): Show |
6 | a0001c0001t0001g0130 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
6 | HG01256.hp1 HG01891.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.569-12044_569-1203 others(18): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(9): Show |
5 | a0001c0001t0001g0253 a0001c0001t0001g0285 a0001c0001t0001g0286 others(2): Show |
5 | HG04199.hp1 NA18947.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-12046_569-1203 others(20): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(11): Show |
3 | a0001c0001t0001g0248 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02809.hp1 HG03209.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.569-12048_569-1203 others(22): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(13): Show |
3 | a0001c0001t0001g0291 a0001c0001t0001g0305 a0001c0001t0012g0006 |
3 | HG02145.hp2 HG04228.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.569-12050_569-1203 others(24): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(15): Show |
2 | a0001c0001t0001g0127 a0001c0003t0001g0155 |
2 | HG00609.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.569-12052_569-1203 others(26): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(17): Show |
7 | a0001c0001t0001g0135 a0001c0001t0001g0146 a0001c0001t0001g0232 others(4): Show |
7 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-12054_569-1203 others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(19): Show |
1 | a0001c0001t0001g0223 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.569-12056_569-1203 others(30): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(21): Show |
6 | a0001c0001t0001g0101 a0001c0001t0001g0121 a0001c0001t0001g0123 others(3): Show |
6 | HG01952.hp1 HG02602.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.569-12058_569-1203 others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(23): Show |
4 | a0001c0001t0001g0104 a0001c0001t0001g0122 a0001c0001t0001g0125 others(1): Show |
4 | HG01934.hp1 HG02258.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.569-12060_569-1203 others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(25): Show |
3 | a0001c0001t0001g0145 a0001c0001t0001g0215 a0001c0001t0001g0233 |
3 | HG02970.hp1 HG02976.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(27): Show |
8 | a0001c0001t0001g0016 a0001c0001t0001g0120 a0001c0001t0001g0126 others(5): Show |
8 | HG01257.hp1 HG01993.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(38): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(29): Show |
14 | a0001c0001t0001g0106 a0001c0001t0001g0111 a0001c0001t0001g0128 others(11): Show |
14 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(40): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(31): Show |
5 | a0001c0001t0001g0133 a0001c0001t0001g0154 a0001c0001t0001g0216 others(2): Show |
5 | HG00642.hp2 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(33): Show |
7 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0137 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(44): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(35): Show |
4 | a0001c0001t0001g0107 a0001c0001t0001g0141 a0001c0001t0001g0236 others(1): Show |
4 | HG01123.hp1 HG02165.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(46): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(37): Show |
2 | a0001c0001t0001g0118 a0001c0001t0001g0132 |
2 | NA18975.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(48): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(39): Show |
4 | a0001c0001t0001g0140 a0001c0001t0001g0220 a0001c0001t0001g0225 others(1): Show |
4 | HG02818.hp2 NA18747.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(50): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(41): Show |
6 | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0119 others(3): Show |
6 | HG01934.hp2 HG02145.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(52): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(43): Show |
1 | a0001c0001t0001g0142 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.569-12031_569-1203 others(54): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(45): Show |
1 | a0001c0001t0001g0235 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.569-12031_569-1203 others(56): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469693 | G | GACACACA others(51): Show |
1 | a0001c0001t0001g0227 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.569-12031_569-1203 others(62): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | ||||||
| chr15:66469723 | C | CACACACA others(45): Show |
1 | a0001c0001t0002g0063 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.569-12031_569-1203 others(56): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(43): Show |
2 | a0001c0001t0002g0050 a0001c0001t0005g0239 |
2 | NA18963.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(54): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(41): Show |
4 | a0001c0001t0002g0060 a0001c0001t0002g0084 a0001c0001t0002g0091 others(1): Show |
4 | HG02056.hp2 NA18993.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(52): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(39): Show |
5 | a0001c0001t0002g0054 a0001c0001t0002g0076 a0001c0001t0002g0093 others(2): Show |
5 | HG03942.hp2 NA18962.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(50): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(41): Show |
2 | a0001c0001t0002g0052 a0001c0001t0003g0206 |
2 | NA18986.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(52): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(37): Show |
3 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 |
3 | HG01243.hp1 NA18946.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(48): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(35): Show |
9 | a0001c0001t0002g0051 a0001c0001t0002g0055 a0001c0001t0002g0058 others(6): Show |
9 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(46): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(33): Show |
11 | a0001c0001t0001g0213 a0001c0001t0002g0012 a0001c0001t0002g0059 others(8): Show |
11 | HG00099.hp2 HG00597.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(44): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(31): Show |
5 | a0001c0001t0002g0049 a0001c0001t0002g0053 a0001c0001t0002g0072 others(2): Show |
5 | NA18954.hp2 NA19012.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(33): Show |
1 | a0001c0001t0005g0160 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.569-12031_569-1203 others(44): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(29): Show |
7 | a0001c0001t0002g0069 a0001c0001t0002g0074 a0001c0001t0002g0082 others(4): Show |
7 | HG00280.hp1 HG00544.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(40): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(27): Show |
6 | a0001c0001t0002g0048 a0001c0001t0002g0062 a0001c0001t0002g0070 others(3): Show |
6 | HG00140.hp2 HG02300.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(38): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(25): Show |
2 | a0001c0001t0005g0243 a0001c0001t0008g0073 |
2 | HG00438.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(23): Show |
2 | a0001c0001t0002g0067 a0001c0001t0005g0158 |
2 | HG03669.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(25): Show |
1 | a0001c0001t0005g0161 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.569-12031_569-1203 others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(21): Show |
2 | a0001c0001t0002g0068 a0001c0005t0002g0087 |
2 | HG00673.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(19): Show |
1 | a0001c0001t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.569-12031_569-1203 others(30): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(17): Show |
4 | a0001c0001t0002g0083 a0001c0001t0002g0088 a0001c0001t0003g0192 others(1): Show |
4 | HG00140.hp1 HG02165.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(15): Show |
2 | a0001c0001t0002g0150 a0001c0001t0003g0183 |
2 | NA18982.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(26): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(13): Show |
4 | a0001c0001t0003g0187 a0001c0001t0003g0199 a0001c0001t0003g0200 others(1): Show |
4 | HG01433.hp2 HG02572.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(24): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(11): Show |
8 | a0001c0001t0002g0075 a0001c0001t0003g0168 a0001c0001t0003g0178 others(5): Show |
8 | HG00642.hp1 HG01168.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(22): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(9): Show |
25 | a0001c0001t0003g0163 a0001c0001t0003g0167 a0001c0001t0003g0174 others(22): Show |
25 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(20): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(7): Show |
3 | a0001c0001t0003g0172 a0001c0001t0003g0173 a0001c0001t0003g0195 |
3 | HG00099.hp1 HG00741.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(18): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(5): Show |
4 | a0001c0001t0003g0166 a0001c0001t0003g0170 a0001c0001t0003g0197 others(1): Show |
4 | HG00738.hp1 HG01074.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469723 | C | CACACACA others(3): Show |
2 | a0001c0001t0003g0191 a0001c0001t0003g0371 |
2 | HG00323.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | ||||||
| chr15:66469725 | T | C | 10 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.569-12030T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469725 | |||||||
| chr15:66469829 | T | A | 4 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(1): Show |
4 | HG00438.hp2 NA18963.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.569-11926T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469829 | |||||||
| chr15:66469855 | C | G | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.569-11900C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469855 | |||||||
| chr15:66469947 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(113): Show |
117 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.569-11808T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469947 | |||||||
| chr15:66469962 | C | A | 1 | a0001c0001t0006g0010 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.569-11793C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469962 | |||||||
| chr15:66470091 | CTTGT | C | 9 | a0001c0001t0003g0206 a0001c0001t0005g0157 a0001c0001t0005g0158 others(6): Show |
9 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.569-11661_569-1165 others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470091 | ||||||
| chr15:66470094 | G | GT | 48 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0036 others(45): Show |
48 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.569-11637dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | ||||||
| chr15:66470094 | G | GTT | 12 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0003g0166 others(9): Show |
12 | HG00099.hp1 HG00597.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.569-11638_569-1163 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | ||||||
| chr15:66470094 | GT | G | 36 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(33): Show |
36 | HG00609.hp2 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.569-11637delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | ||||||
| chr15:66470094 | GTT | G | 44 | a0001c0001t0001g0002 a0001c0001t0001g0046 a0001c0001t0001g0115 others(41): Show |
44 | HG00280.hp2 HG00544.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.569-11638_569-1163 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | ||||||
| chr15:66470094 | GTTT | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(94): Show |
98 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.569-11639_569-1163 others(7): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | ||||||
| chr15:66470094 | GTTTT | G | 47 | a0001c0001t0001g0111 a0001c0001t0001g0213 a0001c0001t0001g0222 others(44): Show |
47 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.569-11640_569-1163 others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | ||||||
| chr15:66470094 | GTTTTT | G | 10 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.569-11641_569-1163 others(9): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | ||||||
| chr15:66470094 | GTTTTTT | G | 35 | a0001c0001t0001g0011 a0001c0001t0001g0326 a0001c0001t0001g0327 others(32): Show |
35 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.569-11642_569-1163 others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | ||||||
| chr15:66470288 | G | C | 2 | a0001c0001t0003g0183 a0001c0001t0003g0187 |
2 | NA18747.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.569-11467G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66470288 | |||||||
| chr15:66470404 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(80): Show |
84 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.569-11351C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66470404 | |||||||
| chr15:66470758 | T | C | 19 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0019 others(16): Show |
19 | HG00423.hp1 HG03927.hp2 NA18941.hp1 others(16): Show |
intron_variant | MODIFIER | c.569-10997T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66470758 | |||||||
| chr15:66470839 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(47): Show |
51 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.569-10916C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66470839 | |||||||
| chr15:66470927 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.569-10828G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66470927 | |||||||
| chr15:66471177 | C | T | 1 | a0001c0001t0003g0211 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.569-10578C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66471177 | |||||||
| chr15:66471302 | C | G | 7 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-10453C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66471302 | |||||||
| chr15:66471363 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.569-10392T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66471363 | |||||||
| chr15:66471618 | G | T | 1 | a0001c0001t0003g0187 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.569-10137G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66471618 | |||||||
| chr15:66471658 | AT | A | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(311): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.569-10086delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66471658 | ||||||
| chr15:66471658 | ATT | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-10087_569-1008 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66471658 | ||||||
| chr15:66471879 | C | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0299 |
2 | HG00609.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.569-9876C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66471879 | |||||||
| chr15:66471937 | C | T | 2 | a0001c0001t0003g0178 a0001c0001t0003g0179 |
2 | HG03490.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.569-9818C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66471937 | |||||||
| chr15:66472075 | C | CA | 9 | a0001c0001t0001g0115 a0001c0001t0001g0123 a0001c0001t0001g0156 others(6): Show |
9 | HG01074.hp2 HG01934.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.569-9662dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472075 | ||||||
| chr15:66472075 | C | CAA | 180 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0111 others(177): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.569-9663_569-9662d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472075 | ||||||
| chr15:66472075 | C | CAAA | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(113): Show |
117 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.569-9664_569-9662d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472075 | ||||||
| chr15:66472075 | C | CAAAA | 14 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0101 others(11): Show |
14 | HG00438.hp1 HG01167.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.569-9665_569-9662d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472075 | ||||||
| chr15:66472075 | C | CAAAAAAA others(2): Show |
7 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(4): Show |
7 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-9670_569-9662d others(11): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472075 | ||||||
| chr15:66472075 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0012g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.569-9671_569-9662d others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472075 | ||||||
| chr15:66472228 | C | A | 1 | a0001c0001t0002g0066 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.569-9527C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472228 | |||||||
| chr15:66472259 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.569-9496G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472259 | |||||||
| chr15:66472303 | C | CA | 112 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0102 others(109): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.569-9437dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472303 | ||||||
| chr15:66472303 | CA | C | 68 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(65): Show |
68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.569-9437delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472303 | ||||||
| chr15:66472430 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-9325C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472430 | |||||||
| chr15:66472452 | A | G | 2 | a0001c0001t0006g0008 a0001c0001t0006g0009 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.569-9303A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472452 | |||||||
| chr15:66472476 | C | A | 20 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0219 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.569-9279C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472476 | |||||||
| chr15:66472535 | C | T | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(320): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.569-9220C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472535 | |||||||
| chr15:66472557 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-9198C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472557 | |||||||
| chr15:66472612 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-9143C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472612 | |||||||
| chr15:66472686 | A | ATTGTCAG | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-9063_569-9062i others(9): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472686 | ||||||
| chr15:66472720 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.569-9035C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472720 | |||||||
| chr15:66472725 | T | C | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.569-9030T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472725 | |||||||
| chr15:66472852 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.569-8903A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472852 | |||||||
| chr15:66472861 | G | A | 1 | a0001c0001t0001g0352 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.569-8894G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472861 | |||||||
| chr15:66472946 | C | T | 1 | a0001c0002t0001g0297 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.569-8809C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472946 | |||||||
| chr15:66473066 | G | A | 36 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0102 others(33): Show |
36 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.569-8689G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66473066 | |||||||
| chr15:66473096 | T | A | 2 | a0001c0001t0001g0258 a0001c0001t0001g0278 |
2 | HG00735.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.569-8659T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66473096 | |||||||
| chr15:66473243 | T | C | 32 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(29): Show |
32 | HG00609.hp2 HG00642.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.569-8512T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66473243 | |||||||
| chr15:66473443 | G | T | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.569-8312G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66473443 | |||||||
| chr15:66473596 | A | C | 2 | a0001c0001t0001g0358 a0001c0001t0001g0359 |
2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.569-8159A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66473596 | |||||||
| chr15:66473803 | G | C | 1 | a0001c0001t0002g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.569-7952G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66473803 | |||||||
| chr15:66473921 | A | G | 14 | a0001c0001t0001g0016 a0001c0001t0001g0120 a0001c0001t0001g0121 others(11): Show |
14 | HG00733.hp1 HG01257.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.569-7834A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66473921 | |||||||
| chr15:66474056 | A | T | 1 | a0001c0001t0003g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.569-7699A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474056 | |||||||
| chr15:66474209 | G | T | 59 | a0001c0001t0001g0213 a0001c0001t0002g0012 a0001c0001t0002g0048 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.569-7546G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474209 | |||||||
| chr15:66474372 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.569-7383G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474372 | |||||||
| chr15:66474405 | A | C | 1 | a0001c0001t0001g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.569-7350A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474405 | |||||||
| chr15:66474546 | C | T | 2 | a0001c0001t0001g0341 a0001c0001t0001g0345 |
2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.569-7209C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474546 | |||||||
| chr15:66474722 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.569-7033C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474722 | |||||||
| chr15:66474826 | C | G | 1 | a0001c0001t0004g0044 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.569-6929C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474826 | |||||||
| chr15:66474836 | G | A | 1 | a0001c0001t0003g0204 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.569-6919G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474836 | |||||||
| chr15:66474902 | C | CA | 10 | a0001c0001t0001g0238 a0001c0001t0001g0336 a0001c0001t0006g0003 others(7): Show |
10 | HG00280.hp2 HG00639.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.569-6837dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66474902 | ||||||
| chr15:66474902 | CA | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(191): Show |
195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.569-6837delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66474902 | ||||||
| chr15:66474996 | C | T | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.569-6759C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474996 | |||||||
| chr15:66475181 | A | G | 8 | a0001c0001t0001g0224 a0001c0001t0002g0072 a0001c0001t0002g0113 others(5): Show |
8 | HG01255.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.569-6574A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66475181 | |||||||
| chr15:66475518 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.569-6237G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66475518 | |||||||
| chr15:66475530 | C | G | 20 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0219 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.569-6225C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66475530 | |||||||
| chr15:66475642 | G | A | 7 | a0001c0001t0001g0251 a0001c0001t0001g0259 a0001c0001t0001g0263 others(4): Show |
7 | HG01256.hp1 HG01346.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.569-6113G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66475642 | |||||||
| chr15:66475669 | C | T | 7 | a0001c0001t0002g0072 a0001c0001t0002g0113 a0001c0001t0002g0114 others(4): Show |
7 | HG01255.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.569-6086C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66475669 | |||||||
| chr15:66475707 | G | C | 1 | a0001c0001t0001g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.569-6048G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66475707 | |||||||
| chr15:66475743 | C | T | 1 | a0001c0001t0001g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.569-6012C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66475743 | |||||||
| chr15:66476027 | C | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0326 a0001c0001t0001g0328 others(1): Show |
4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-5728C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476027 | |||||||
| chr15:66476037 | C | T | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.569-5718C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476037 | |||||||
| chr15:66476177 | G | A | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.569-5578G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476177 | |||||||
| chr15:66476265 | A | C | 1 | a0001c0001t0005g0160 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.569-5490A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476265 | |||||||
| chr15:66476280 | T | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0141 |
3 | NA18956.hp1 NA18971.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.569-5475T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476280 | |||||||
| chr15:66476372 | T | C | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.569-5383T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476372 | |||||||
| chr15:66476471 | G | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-5284G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476471 | |||||||
| chr15:66476516 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.569-5239C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476516 | |||||||
| chr15:66476565 | G | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.569-5190G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476565 | |||||||
| chr15:66476664 | A | G | 54 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0102 others(51): Show |
54 | HG00280.hp2 HG00639.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.569-5091A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476664 | |||||||
| chr15:66476691 | G | A | 50 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(47): Show |
50 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.569-5064G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476691 | |||||||
| chr15:66476846 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-4909A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476846 | |||||||
| chr15:66476968 | G | T | 1 | a0001c0001t0002g0068 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.569-4787G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476968 | |||||||
| chr15:66477002 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.569-4753A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477002 | |||||||
| chr15:66477027 | C | T | 26 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0214 others(23): Show |
26 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.569-4728C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477027 | |||||||
| chr15:66477145 | G | C | 2 | a0001c0001t0002g0086 a0001c0001t0002g0096 |
2 | NA19002.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.569-4610G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477145 | |||||||
| chr15:66477256 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0142 |
2 | NA18968.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.569-4499T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477256 | |||||||
| chr15:66477275 | G | A | 26 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0214 others(23): Show |
26 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.569-4480G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477275 | |||||||
| chr15:66477358 | G | A | 1 | a0001c0001t0003g0195 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.569-4397G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477358 | |||||||
| chr15:66477567 | C | T | 38 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(35): Show |
38 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.569-4188C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477567 | |||||||
| chr15:66477591 | C | G | 206 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0102 others(203): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.569-4164C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477591 | |||||||
| chr15:66477710 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(77): Show |
81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.569-4045G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477710 | |||||||
| chr15:66477716 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.569-4039T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477716 | |||||||
| chr15:66477724 | G | A | 1 | a0001c0001t0001g0301 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.569-4031G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477724 | |||||||
| chr15:66477825 | C | T | 62 | a0001c0001t0001g0213 a0001c0001t0002g0012 a0001c0001t0002g0048 others(59): Show |
62 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.569-3930C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477825 | |||||||
| chr15:66477826 | G | A | 50 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(47): Show |
50 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.569-3929G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477826 | |||||||
| chr15:66478002 | C | T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.569-3753C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478002 | |||||||
| chr15:66478164 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-3591C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478164 | |||||||
| chr15:66478238 | T | TTA | 4 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0338 others(1): Show |
4 | HG02615.hp1 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-3504_569-3503d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478238 | ||||||
| chr15:66478253 | A | T | 46 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0102 others(43): Show |
46 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.569-3502A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478253 | |||||||
| chr15:66478276 | CAT | C | 46 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0102 others(43): Show |
46 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.569-3467_569-3466d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478276 | ||||||
| chr15:66478276 | CATAT | C | 3 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0065 |
3 | NA18946.hp2 NA19056.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.569-3469_569-3466d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478276 | ||||||
| chr15:66478288 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-3467T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478288 | |||||||
| chr15:66478313 | GTA | G | 19 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0019 others(16): Show |
19 | HG00423.hp1 HG03927.hp2 NA18941.hp1 others(16): Show |
intron_variant | MODIFIER | c.569-3432_569-3431d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478313 | ||||||
| chr15:66478326 | TTATATAT others(18): Show |
T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.569-3391_569-3367d others(27): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478326 | ||||||
| chr15:66478364 | CAT | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-3386_569-3385d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478364 | ||||||
| chr15:66478392 | A | ATG | 50 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(47): Show |
50 | HG00280.hp2 HG00639.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.569-3355_569-3354d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478392 | ||||||
| chr15:66478400 | G | GTGTA | 4 | a0001c0001t0001g0011 a0001c0001t0001g0326 a0001c0001t0001g0328 others(1): Show |
4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-3354_569-3353i others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478400 | ||||||
| chr15:66478400 | GTA | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG00738.hp2 HG01106.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.569-3342_569-3341d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478400 | ||||||
| chr15:66478402 | A | ATATATAT others(33): Show |
3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.569-3338_569-3299d others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478402 | ||||||
| chr15:66478402 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(44): Show |
48 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.569-3353A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478402 | |||||||
| chr15:66478413 | T | C | 17 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0219 others(14): Show |
17 | HG01069.hp2 HG01071.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.569-3342T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478413 | |||||||
| chr15:66478417 | C | CACAGGTA others(29): Show |
68 | a0001c0001t0001g0213 a0001c0001t0001g0218 a0001c0001t0001g0223 others(65): Show |
68 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.569-3320_569-3285d others(38): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478417 | ||||||
| chr15:66478417 | C | CACAGGTA others(65): Show |
5 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(2): Show |
5 | HG02145.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-3285_569-3284i others(74): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478417 | ||||||
| chr15:66478417 | C | CAGGTATA others(27): Show |
16 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0219 others(13): Show |
16 | HG01069.hp2 HG01071.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.569-3337_569-3336i others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478417 | ||||||
| chr15:66478422 | GTATATAT others(33): Show |
G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-3318_569-3279d others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478422 | ||||||
| chr15:66478433 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.569-3322T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478433 | |||||||
| chr15:66478458 | G | GTA | 7 | a0001c0001t0001g0228 a0001c0001t0001g0336 a0001c0001t0003g0176 others(4): Show |
7 | HG00423.hp1 HG00558.hp1 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.569-3282_569-3281d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478458 | ||||||
| chr15:66478506 | A | AT | 7 | a0001c0001t0001g0142 a0001c0001t0003g0184 a0001c0001t0003g0186 others(4): Show |
7 | HG00099.hp1 HG02602.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-3239dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478506 | ||||||
| chr15:66478506 | A | T | 3 | a0001c0001t0001g0254 a0001c0001t0001g0312 a0001c0003t0001g0155 |
3 | HG00639.hp2 HG01081.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.569-3249A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478506 | |||||||
| chr15:66478507 | T | TA | 6 | a0001c0001t0001g0118 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG01123.hp1 NA18956.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.569-3248_569-3247i others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478507 | |||||||
| chr15:66478508 | T | A | 81 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0035 others(78): Show |
81 | HG00609.hp2 HG00642.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.569-3247T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478508 | |||||||
| chr15:66478510 | T | A | 1 | a0001c0001t0001g0231 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.569-3245T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478510 | |||||||
| chr15:66478521 | CA | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-3232delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478521 | ||||||
| chr15:66478534 | CTT | C | 31 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(28): Show |
31 | HG00609.hp2 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.569-3219_569-3218d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478534 | ||||||
| chr15:66478868 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.569-2887C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478868 | |||||||
| chr15:66478907 | C | T | 1 | a0001c0001t0013g0351 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.569-2848C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478907 | |||||||
| chr15:66479065 | A | G | 2 | a0001c0001t0002g0080 a0001c0001t0002g0081 |
2 | NA18972.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.569-2690A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66479065 | |||||||
| chr15:66479298 | A | T | 1 | a0001c0001t0001g0011 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.569-2457A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66479298 | |||||||
| chr15:66479427 | A | G | 1 | a0001c0001t0003g0208 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.569-2328A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66479427 | |||||||
| chr15:66479504 | G | A | 11 | a0001c0001t0003g0206 a0001c0001t0005g0157 a0001c0001t0005g0158 others(8): Show |
11 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.569-2251G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66479504 | |||||||
| chr15:66479669 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(80): Show |
84 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.569-2086C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66479669 | |||||||
| chr15:66479758 | G | A | 6 | a0001c0001t0001g0118 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | NA18956.hp1 NA18968.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.569-1997G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66479758 | |||||||
| chr15:66479909 | T | C | 2 | a0001c0001t0005g0240 a0001c0001t0005g0243 |
2 | HG00438.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.569-1846T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66479909 | |||||||
| chr15:66480142 | G | A | 13 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(10): Show |
13 | HG00438.hp1 HG00609.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.569-1613G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480142 | |||||||
| chr15:66480220 | A | C | 1 | a0001c0001t0003g0206 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.569-1535A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480220 | |||||||
| chr15:66480234 | G | A | 2 | a0001c0001t0001g0342 a0001c0001t0011g0269 |
2 | HG02040.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.569-1521G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480234 | |||||||
| chr15:66480240 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.569-1515C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480240 | |||||||
| chr15:66480383 | C | T | 16 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0219 others(13): Show |
16 | HG01069.hp2 HG01071.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.569-1372C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480383 | |||||||
| chr15:66480480 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(81): Show |
85 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.569-1275T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480480 | |||||||
| chr15:66480514 | G | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-1241G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480514 | |||||||
| chr15:66480580 | T | A | 3 | a0001c0001t0003g0170 a0001c0001t0003g0196 a0001c0001t0003g0197 |
3 | HG00738.hp1 HG01516.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.569-1175T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480580 | |||||||
| chr15:66480630 | G | A | 2 | a0001c0001t0001g0354 a0001c0001t0001g0355 |
2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.569-1125G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480630 | |||||||
| chr15:66480857 | C | G | 39 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(36): Show |
39 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.569-898C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480857 | |||||||
| chr15:66480939 | A | T | 1 | a0001c0001t0006g0007 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.569-816A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480939 | |||||||
| chr15:66481131 | G | A | 1 | a0001c0001t0003g0195 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.569-624G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481131 | |||||||
| chr15:66481213 | T | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-542T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481213 | |||||||
| chr15:66481344 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.569-411A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481344 | |||||||
| chr15:66481395 | C | A | 26 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0214 others(23): Show |
26 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.569-360C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481395 | |||||||
| chr15:66481414 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.569-341G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481414 | |||||||
| chr15:66481440 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.569-315C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481440 | |||||||
| chr15:66481637 | G | A | 50 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(47): Show |
50 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.569-118G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481637 | |||||||
| chr15:66481676 | T | A | 1 | a0001c0001t0001g0355 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.569-79T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481676 | |||||||
| chr15:66481929 | G | C | 6 | a0001c0001t0001g0118 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | NA18956.hp1 NA18968.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+50G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66481929 | |||||||
| chr15:66482113 | C | A | 4 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+234C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482113 | |||||||
| chr15:66482154 | T | A | 1 | a0001c0001t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.693+275T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482154 | |||||||
| chr15:66482221 | A | G | 329 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(326): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.693+342A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482221 | |||||||
| chr15:66482225 | C | T | 1 | a0001c0001t0001g0339 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.693+346C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482225 | |||||||
| chr15:66482278 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.693+399C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482278 | |||||||
| chr15:66482479 | G | T | 1 | a0001c0002t0001g0297 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.693+600G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482479 | |||||||
| chr15:66482628 | C | T | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.693+749C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482628 | |||||||
| chr15:66482759 | T | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.693+880T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482759 | |||||||
| chr15:66482825 | C | T | 7 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.693+946C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482825 | |||||||
| chr15:66482873 | G | GGCGGGGA others(10): Show |
2 | a0001c0001t0001g0213 a0001c0001t0002g0099 |
2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.693+998_693+1014du others(18): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 66482873 | ||||||
| chr15:66482911 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.693+1032G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482911 | |||||||
| chr15:66482979 | C | T | 1 | a0001c0001t0006g0010 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.693+1100C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482979 | |||||||
| chr15:66483175 | G | C | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.693+1296G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66483175 | |||||||
| chr15:66483250 | G | C | 5 | a0001c0001t0001g0325 a0001c0001t0001g0327 a0001c0001t0001g0329 others(2): Show |
5 | HG02257.hp2 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+1371G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66483250 | |||||||
| chr15:66483555 | T | C | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.694-1435T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66483555 | |||||||
| chr15:66483748 | C | CT | 12 | a0001c0001t0001g0116 a0001c0001t0001g0130 a0001c0001t0001g0152 others(9): Show |
12 | HG01109.hp1 HG01891.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.694-1225dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 66483748 | ||||||
| chr15:66483748 | C | CTTT | 45 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
46 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.694-1227_694-1225d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 66483748 | ||||||
| chr15:66483748 | C | CTTTT | 25 | a0001c0001t0001g0002 a0001c0001t0001g0259 a0001c0001t0001g0279 others(22): Show |
25 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.694-1228_694-1225d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 66483748 | ||||||
| chr15:66483899 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.694-1091C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66483899 | |||||||
| chr15:66483908 | C | T | 49 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(46): Show |
49 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.694-1082C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66483908 | |||||||
| chr15:66483921 | TG | T | 3 | a0001c0001t0001g0248 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.694-1068delG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66483921 | |||||||
| chr15:66483997 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.694-993C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66483997 | |||||||
| chr15:66484102 | A | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(320): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.694-888A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484102 | |||||||
| chr15:66484139 | A | AC | 47 | a0001c0001t0001g0011 a0001c0001t0001g0111 a0001c0001t0001g0156 others(44): Show |
47 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.694-842dupC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 66484139 | ||||||
| chr15:66484142 | C | A | 62 | a0001c0001t0001g0213 a0001c0001t0001g0234 a0001c0001t0002g0012 others(59): Show |
62 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.694-848C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484142 | |||||||
| chr15:66484142 | C | T | 1 | a0001c0001t0003g0168 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.694-848C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484142 | |||||||
| chr15:66484146 | C | A | 1 | a0001c0001t0001g0031 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.694-844C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484146 | |||||||
| chr15:66484146 | C | G | 1 | a0001c0001t0001g0299 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.694-844C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484146 | |||||||
| chr15:66484291 | G | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-699G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484291 | |||||||
| chr15:66484316 | T | C | 2 | a0001c0001t0007g0056 a0001c0001t0007g0057 |
2 | HG01255.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.694-674T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484316 | |||||||
| chr15:66484423 | C | T | 1 | a0001c0001t0002g0071 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.694-567C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484423 | |||||||
| chr15:66484444 | C | T | 9 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(6): Show |
9 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.694-546C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484444 | |||||||
| chr15:66484501 | G | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-489G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484501 | |||||||
| chr15:66484668 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0001g0233 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.694-322G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484668 | |||||||
| chr15:66484681 | TGGCCAAG others(3): Show |
T | 36 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(33): Show |
36 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.694-306_694-297del others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 66484681 | ||||||
| chr15:66484685 | C | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.694-305C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484685 | |||||||
| chr15:66484842 | G | C | 1 | a0001c0001t0001g0339 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.694-148G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484842 | |||||||
| chr15:66484977 | G | GTC | 7 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.694-8_694-7dupTC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 66484977 | ||||||
| chr15:66485252 | G | A | 1 | a0001c0001t0001g0337 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.895+61G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485252 | |||||||
| chr15:66485253 | G | A | 1 | a0001c0001t0001g0337 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.895+62G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485253 | |||||||
| chr15:66485342 | G | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.895+151G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485342 | |||||||
| chr15:66485372 | A | G | 7 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.895+181A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485372 | |||||||
| chr15:66485590 | G | A | 1 | a0001c0001t0002g0049 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.895+399G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485590 | |||||||
| chr15:66485622 | A | G | 37 | a0001c0001t0001g0011 a0001c0001t0001g0325 a0001c0001t0001g0326 others(34): Show |
37 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.895+431A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485622 | |||||||
| chr15:66485828 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.895+637C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485828 | |||||||
| chr15:66485904 | T | G | 2 | a0001c0001t0001g0304 a0001c0001t0001g0306 |
2 | HG01952.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.895+713T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485904 | |||||||
| chr15:66486073 | A | T | 6 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(3): Show |
6 | HG00558.hp1 HG00673.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.895+882A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486073 | |||||||
| chr15:66486143 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.895+952C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486143 | |||||||
| chr15:66486279 | C | T | 53 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0102 others(50): Show |
53 | HG00280.hp2 HG00639.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.896-949C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486279 | |||||||
| chr15:66486450 | T | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.896-778T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486450 | |||||||
| chr15:66486484 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0326 a0001c0001t0001g0328 others(1): Show |
4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.896-744G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486484 | |||||||
| chr15:66486488 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.896-740A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486488 | |||||||
| chr15:66486700 | A | T | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.896-528A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486700 | |||||||
| chr15:66486732 | G | A | 1 | a0001c0001t0001g0337 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.896-496G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486732 | |||||||
| chr15:66486829 | A | G | 331 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(328): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.896-399A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486829 | |||||||
| chr15:66486937 | G | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.896-291G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486937 | |||||||
| chr15:66487115 | G | A | 1 | a0001c0001t0002g0052 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.896-113G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66487115 | |||||||
| chr15:66487360 | C | T | 27 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0214 others(24): Show |
27 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.960+68C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66487360 | |||||||
| chr15:66487506 | G | T | 1 | a0001c0001t0001g0245 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.960+214G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66487506 | |||||||
| chr15:66487739 | T | C | 27 | a0001c0001t0001g0108 a0001c0001t0001g0341 a0001c0001t0001g0342 others(24): Show |
27 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.960+447T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66487739 | |||||||
| chr15:66487890 | G | A | 1 | a0001c0001t0001g0286 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.960+598G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66487890 | |||||||
| chr15:66488112 | GT | G | 25 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(22): Show |
25 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.960+822delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 66488112 | ||||||
| chr15:66488126 | G | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+834G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66488126 | |||||||
| chr15:66488360 | G | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0119 others(27): Show |
30 | HG00609.hp2 HG00642.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.961-855G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66488360 | |||||||
| chr15:66488413 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(80): Show |
84 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.961-802C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66488413 | |||||||
| chr15:66488951 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.961-264A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66488951 | |||||||
| chr15:66488960 | CAAGT | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.961-254_961-251del others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66488960 | |||||||
| chr15:66489023 | A | G | 2 | a0001c0001t0003g0167 a0001c0001t0003g0209 |
2 | NA18940.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.961-192A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66489023 | |||||||
| chr15:66489499 | G | C | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1023-219G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 9/10 | chr15 | 66489499 | |||||||
| chr15:66489516 | AC | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1023-201delC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 9/10 | chr15 | 66489516 | |||||||
| chr15:66489675 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1023-43C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 9/10 | chr15 | 66489675 | |||||||
| chr15:66489710 | C | T | 26 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0214 others(23): Show |
26 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(23): Show |
splice_region_variant&intron_variant | LOW | c.1023-8C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 9/10 | chr15 | 66489710 | |||||||
| chr15:66489922 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1068+159C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 10/10 | chr15 | 66489922 | |||||||
| chr15:66490090 | CAG | C | 6 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068+330_1068+331d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 66490090 | ||||||
| chr15:66490103 | C | T | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0002g0067 |
3 | NA18946.hp1 NA18949.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1068+340C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 10/10 | chr15 | 66490103 | |||||||
| chr15:66490132 | A | G | 2 | a0001c0001t0001g0343 a0001c0001t0001g0344 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1068+369A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 10/10 | chr15 | 66490132 | |||||||
| chr15:66490183 | G | A | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1069-319G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 10/10 | chr15 | 66490183 | |||||||
| chr15:66490239 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1069-263G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 10/10 | chr15 | 66490239 |