Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8491 |
| ensemblid | ENSG00000011566.15 |
| hgncid | 6865 |
| symbol | MAP4K3 |
| name | mitogen-activated protein kinase kinase kinase kinase 3 |
| refseq_nuc | NM_003618.4 |
| refseq_prot | NP_003609.2 |
| ensembl_nuc | ENST00000263881.8 |
| ensembl_prot | ENSP00000263881.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 39249266 |
| end | 39437285 |
| strand | - |
| ver | v1.2 |
| region | chr2:39249266-39437285 |
| region5000 | chr2:39244266-39442285 |
| regionname0 | MAP4K3_chr2_39249266_39437285 |
| regionname5000 | MAP4K3_chr2_39244266_39442285 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 894 | 229 | 74 | 44 | 73 | 6 | 30 | 63 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | MNPGF others(889): Show |
chr2 | 39244266 | 39442285 |
| a0002 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | MNPGF others(889): Show |
chr2 | 39244266 | 39442285 |
| a0003 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | MNPGF others(889): Show |
chr2 | 39244266 | 39442285 |
| a0004 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | MNPGF others(889): Show |
chr2 | 39244266 | 39442285 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2682 | 113 | 54 | 19 | 30 | 1 | 8 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | ATGAA others(2677): Show |
chr2 | 39244266 | 39442285 | ||
| a0001c0002 | 0/1 | 2682 | 90 | 13 | 22 | 32 | 4 | 18 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | ATGAA others(2677): Show |
chr2 | 39244266 | 39442285 | ||
| a0001c0003 | 0/0 | 2682 | 20 | 4 | 1 | 10 | 1 | 4 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | ATGAA others(2677): Show |
chr2 | 39244266 | 39442285 | ||
| a0001c0004 | 0/0 | 2682 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | ATGAA others(2677): Show |
chr2 | 39244266 | 39442285 | ||
| a0001c0005 | 0/0 | 2682 | 2 | 1 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | ATGAA others(2677): Show |
chr2 | 39244266 | 39442285 | ||
| a0001c0007 | 0/0 | 2682 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | ATGAA others(2677): Show |
chr2 | 39244266 | 39442285 | ||
| a0001c0008 | 0/0 | 2682 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | ATGAA others(2677): Show |
chr2 | 39244266 | 39442285 | ||
| a0002c0010 | 0/0 | 2682 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | ATGAA others(2677): Show |
chr2 | 39244266 | 39442285 | ||
| a0003c0009 | 0/0 | 2682 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | ATGAA others(2677): Show |
chr2 | 39244266 | 39442285 | ||
| a0004c0006 | 0/0 | 2682 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | ATGAA others(2677): Show |
chr2 | 39244266 | 39442285 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0001t0002 | 1/0 | 4335 | 65 | 20 | 14 | 22 | 0 | 8 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0001t0003 | 0/0 | 4335 | 24 | 22 | 2 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0001t0005 | 0/0 | 4335 | 9 | 9 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0001t0006 | 0/0 | 4335 | 8 | 0 | 1 | 7 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0001t0008 | 0/0 | 4335 | 3 | 0 | 2 | 0 | 1 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0001t0014 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0001t0015 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0001t0016 | 0/0 | 4338 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4333): Show |
chr2 | 39244266 | 39442285 |
| a0001c0002t0001 | 0/1 | 4335 | 81 | 9 | 21 | 29 | 4 | 17 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0002t0007 | 0/0 | 4341 | 3 | 2 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4336): Show |
chr2 | 39244266 | 39442285 |
| a0001c0002t0009 | 0/0 | 4335 | 3 | 2 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0002t0010 | 0/0 | 4338 | 3 | 0 | 0 | 2 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4333): Show |
chr2 | 39244266 | 39442285 |
| a0001c0003t0002 | 0/0 | 4335 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0003t0004 | 0/0 | 4341 | 14 | 0 | 1 | 9 | 1 | 3 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4336): Show |
chr2 | 39244266 | 39442285 |
| a0001c0003t0005 | 0/0 | 4335 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0003t0007 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4336): Show |
chr2 | 39244266 | 39442285 |
| a0001c0003t0011 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0003t0012 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0004t0005 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0004t0013 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0005t0002 | 0/0 | 4335 | 2 | 1 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0007t0001 | 0/0 | 4335 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0001c0008t0002 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0002c0010t0005 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0003c0009t0005 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4330): Show |
chr2 | 39244266 | 39442285 |
| a0004c0006t0004 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | GGAAG others(4336): Show |
chr2 | 39244266 | 39442285 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0008g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0008g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0014g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0015g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0001t0016g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0007g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0007g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0009g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0010g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0010g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0002t0010g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0004g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0007g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0011g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0003t0012g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0004t0005g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0004t0013g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0005t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0005t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0007t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0001c0008t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0002c0010t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0003c0009t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| a0004c0006t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0003 | t0004 | g0227 | EUR | GBR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0120 | EUR | GBR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0049 | EUR | FIN | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0095 | EUR | FIN | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG00408 | hp1 | a0001 | c0003 | t0004 | g0218 | EAS | CHS | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | CHS | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | CHS | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG00738 | hp1 | a0001 | c0001 | t0008 | g0050 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0051 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01099 | hp1 | a0001 | c0007 | t0001 | g0048 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0150 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01109 | hp2 | a0001 | c0002 | t0007 | g0224 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01243 | hp1 | a0001 | c0005 | t0002 | g0034 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | CLM | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0073 | AMR | CLM | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0086 | AMR | CLM | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0113 | AMR | CLM | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | CLM | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0138 | AMR | CLM | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0198 | AMR | CLM | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | CLM | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01884 | hp1 | a0001 | c0003 | t0005 | g0006 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01884 | hp2 | a0001 | c0005 | t0002 | g0033 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0064 | AMR | PEL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01934 | hp1 | a0001 | c0003 | t0004 | g0222 | AMR | PEL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | PEL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | PEL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0084 | AMR | PEL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0144 | AMR | PEL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PEL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02055 | hp1 | a0001 | c0002 | t0007 | g0230 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | KHV | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02129 | hp2 | a0001 | c0003 | t0004 | g0232 | EAS | KHV | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | KHV | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02132 | hp2 | a0001 | c0003 | t0004 | g0216 | EAS | KHV | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CDX | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02165 | hp2 | a0001 | c0002 | t0010 | g0213 | EAS | CDX | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0121 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0114 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PEL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | PEL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0142 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02615 | hp1 | a0002 | c0010 | t0005 | g0017 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02647 | hp1 | a0003 | c0009 | t0005 | g0016 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0149 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02886 | hp1 | a0001 | c0003 | t0012 | g0004 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02895 | hp1 | a0001 | c0004 | t0005 | g0002 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02896 | hp1 | a0001 | c0002 | t0009 | g0087 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02922 | hp1 | a0001 | c0001 | t0015 | g0192 | AFR | ESN | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | ESN | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | ESN | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | ESN | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0112 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0177 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ESN | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | ESN | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03195 | hp2 | a0001 | c0002 | t0009 | g0041 | AFR | ESN | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03209 | hp1 | a0001 | c0003 | t0011 | g0001 | AFR | MSL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | MSL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | MSL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0207 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0089 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | MSL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03453 | hp2 | a0001 | c0004 | t0013 | g0003 | AFR | MSL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | MSL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03490 | hp2 | a0001 | c0003 | t0004 | g0226 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03492 | hp1 | a0001 | c0003 | t0004 | g0225 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0076 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | MSL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | MSL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0147 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03710 | hp1 | a0001 | c0003 | t0002 | g0091 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0075 | SAS | PJL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0151 | SAS | BEB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | BEB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | BEB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03834 | hp2 | a0001 | c0002 | t0010 | g0210 | SAS | BEB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03927 | hp1 | a0001 | c0003 | t0004 | g0215 | SAS | BEB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0131 | SAS | BEB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0132 | SAS | STU | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | STU | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | STU | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | STU | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | YRI | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | YRI | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18945 | hp2 | a0001 | c0001 | t0006 | g0199 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18952 | hp2 | a0001 | c0001 | t0006 | g0204 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18953 | hp1 | a0001 | c0003 | t0004 | g0229 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18954 | hp2 | a0001 | c0003 | t0004 | g0214 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18959 | hp1 | a0001 | c0003 | t0004 | g0217 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18959 | hp2 | a0001 | c0002 | t0010 | g0211 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18961 | hp2 | a0004 | c0006 | t0004 | g0220 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18965 | hp2 | a0001 | c0001 | t0006 | g0201 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18973 | hp1 | a0001 | c0003 | t0004 | g0231 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18975 | hp1 | a0001 | c0003 | t0004 | g0219 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18981 | hp1 | a0001 | c0001 | t0006 | g0200 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18983 | hp2 | a0001 | c0003 | t0004 | g0228 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18989 | hp1 | a0001 | c0001 | t0006 | g0203 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18998 | hp1 | a0001 | c0003 | t0007 | g0221 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19012 | hp2 | a0001 | c0008 | t0002 | g0088 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | LWK | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19030 | hp2 | a0001 | c0002 | t0007 | g0223 | AFR | LWK | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | LWK | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | LWK | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19070 | hp1 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19078 | hp2 | a0001 | c0001 | t0006 | g0205 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19079 | hp2 | a0001 | c0002 | t0009 | g0129 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19088 | hp2 | a0001 | c0001 | t0016 | g0212 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | YRI | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA19240 | hp2 | a0001 | c0001 | t0014 | g0189 | AFR | YRI | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | ASW | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | ASW | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0146 | EUR | TSI | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0115 | EUR | TSI | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | GIH | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0046 | SAS | GIH | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02109 | hp1 | a0001 | c0003 | t0005 | g0005 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0184 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | ACB | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | MSL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | USA | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | USA | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | LWK | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | LWK | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0110 | REF | REF | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0162 | REF | REF | MAP4K3_chr2_39244266_39442285 | MAP4K3 | chr2 | 39244266 | 39442285 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:39265294 | T | A | 1 | a0004 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.2045A>T | p.Tyr682Phe | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/34 | 2343/4335 | 2045/2685 | 682/894 | chr2 | 39265294 | |||
| chr2:39315343 | C | A | 1 | a0002 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.964G>T | p.Val322Leu | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/34 | 1262/4335 | 964/2685 | 322/894 | chr2 | 39315343 | |||
| chr2:39325589 | T | C | 1 | a0003 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.847A>G | p.Ile283Val | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/34 | 1145/4335 | 847/2685 | 283/894 | chr2 | 39325589 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:39250702 | G | A | 1 | a0001c0007 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.2601C>T | p.Val867Val | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 34/34 | 2899/4335 | 2601/2685 | 867/894 | chr2 | 39250702 | |||
| chr2:39251838 | T | C | 1 | a0001c0005 | 2 | HG01243.hp1 HG01884.hp2 |
synonymous_variant | LOW | c.2589A>G | p.Gly863Gly | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 33/34 | 2887/4335 | 2589/2685 | 863/894 | chr2 | 39251838 | |||
| chr2:39280276 | T | A | 3 | a0001c0002 a0001c0007 a0001c0008 |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
synonymous_variant | LOW | c.1710A>T | p.Thr570Thr | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/34 | 2008/4335 | 1710/2685 | 570/894 | chr2 | 39280276 | |||
| chr2:39325910 | A | G | 1 | a0001c0004 | 2 | HG02895.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.714T>C | p.Asp238Asp | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 10/34 | 1012/4335 | 714/2685 | 238/894 | chr2 | 39325910 | |||
| chr2:39356305 | A | G | 4 | a0001c0002 a0001c0003 a0001c0007 others(1): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
synonymous_variant | LOW | c.189T>C | p.Ile63Ile | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/34 | 487/4335 | 189/2685 | 63/894 | chr2 | 39356305 | |||
| chr2:39436976 | G | A | 1 | a0002c0010 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.12C>T | p.Gly4Gly | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/34 | 310/4335 | 12/2685 | 4/894 | chr2 | 39436976 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:39249278 | G | A | 1 | a0001c0001t0006 | 8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1340C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 34/34 | 1340 | chr2 | 39249278 | ||||||
| chr2:39249341 | T | C | 8 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0007 others(5): Show |
93 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1277A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 34/34 | 1277 | chr2 | 39249341 | ||||||
| chr2:39249583 | T | C | 1 | a0001c0004t0013 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1035A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 34/34 | 1035 | chr2 | 39249583 | ||||||
| chr2:39249804 | C | T | 1 | a0001c0003t0012 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*814G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 34/34 | 814 | chr2 | 39249804 | ||||||
| chr2:39249833 | G | A | 1 | a0001c0004t0013 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*785C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 34/34 | 785 | chr2 | 39249833 | ||||||
| chr2:39249861 | T | C | 1 | a0001c0002t0009 | 3 | HG02896.hp1 HG03195.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*757A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 34/34 | 757 | chr2 | 39249861 | ||||||
| chr2:39250029 | T | C | 10 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 others(7): Show |
118 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*589A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 34/34 | 589 | chr2 | 39250029 | ||||||
| chr2:39250049 | G | C | 1 | a0001c0001t0015 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*569C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 34/34 | 569 | chr2 | 39250049 | ||||||
| chr2:39250147 | A | G | 1 | a0001c0001t0008 | 3 | HG00280.hp1 HG00738.hp1 HG01081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*471T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 34/34 | 471 | chr2 | 39250147 | ||||||
| chr2:39250252 | C | T | 1 | a0001c0001t0014 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*366G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 34/34 | 366 | chr2 | 39250252 | ||||||
| chr2:39250461 | T | A | 1 | a0001c0001t0006 | 8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*157A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 34/34 | 157 | chr2 | 39250461 | ||||||
| chr2:39437003 | C | G | 7 | a0001c0001t0005 a0001c0003t0005 a0001c0003t0012 others(4): Show |
16 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-16G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/34 | 16 | chr2 | 39437003 | ||||||
| chr2:39437024 | A | T | 1 | a0001c0003t0011 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-37T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/34 | 37 | chr2 | 39437024 | ||||||
| chr2:39437120 | G | GGCC | 2 | a0001c0001t0016 a0001c0002t0010 |
4 | HG02165.hp2 HG03834.hp2 NA18959.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-136_-134dupGGC | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/34 | 134 | chr2 | 39437120 | ||||||
| chr2:39437120 | G | GGCCGCC | 4 | a0001c0002t0007 a0001c0003t0004 a0001c0003t0007 others(1): Show |
19 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-139_-134dupGGCGGC | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/34 | 134 | chr2 | 39437120 | ||||||
| chr2:39437239 | G | A | 4 | a0001c0002t0007 a0001c0003t0004 a0001c0003t0007 others(1): Show |
19 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-252C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/34 | 252 | chr2 | 39437239 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:39250757 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2598-52A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 33/33 | chr2 | 39250757 | |||||||
| chr2:39250964 | T | A | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2598-259A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 33/33 | chr2 | 39250964 | |||||||
| chr2:39251089 | A | G | 1 | a0001c0003t0004g0228 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2598-384T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 33/33 | chr2 | 39251089 | |||||||
| chr2:39251100 | G | A | 4 | a0001c0002t0001g0134 a0001c0002t0001g0195 a0001c0002t0001g0196 others(1): Show |
4 | NA18986.hp2 NA19054.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.2598-395C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 33/33 | chr2 | 39251100 | |||||||
| chr2:39251151 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2598-446G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 33/33 | chr2 | 39251151 | |||||||
| chr2:39251243 | A | T | 175 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.2598-538T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 33/33 | chr2 | 39251243 | |||||||
| chr2:39251565 | T | C | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2597+265A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 33/33 | chr2 | 39251565 | |||||||
| chr2:39251634 | C | A | 1 | a0001c0002t0001g0131 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2597+196G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 33/33 | chr2 | 39251634 | |||||||
| chr2:39251691 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2597+139G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 33/33 | chr2 | 39251691 | |||||||
| chr2:39251916 | G | A | 1 | a0001c0002t0010g0213 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2542-31C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39251916 | |||||||
| chr2:39251980 | C | A | 2 | a0001c0001t0002g0099 a0001c0001t0002g0137 |
2 | HG01496.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.2542-95G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39251980 | |||||||
| chr2:39251981 | G | C | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.2542-96C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39251981 | |||||||
| chr2:39251991 | A | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2542-106T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39251991 | |||||||
| chr2:39252064 | T | C | 13 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0159 others(10): Show |
13 | HG02622.hp1 HG02717.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.2542-179A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39252064 | |||||||
| chr2:39252078 | T | G | 1 | a0001c0002t0001g0138 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2542-193A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39252078 | |||||||
| chr2:39252285 | G | C | 1 | a0001c0002t0001g0046 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2542-400C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39252285 | |||||||
| chr2:39252289 | T | A | 1 | a0001c0001t0002g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2542-404A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39252289 | |||||||
| chr2:39252320 | C | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2542-435G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39252320 | |||||||
| chr2:39252347 | C | T | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2542-462G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39252347 | |||||||
| chr2:39252359 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2542-474C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39252359 | |||||||
| chr2:39252839 | T | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2542-954A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39252839 | |||||||
| chr2:39252864 | C | T | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2542-979G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39252864 | |||||||
| chr2:39253074 | C | T | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.2542-1189G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39253074 | |||||||
| chr2:39253176 | G | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2541+1274C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39253176 | |||||||
| chr2:39253290 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2541+1160G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39253290 | |||||||
| chr2:39253375 | G | A | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.2541+1075C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39253375 | |||||||
| chr2:39253451 | C | T | 20 | a0001c0001t0003g0173 a0001c0001t0003g0174 a0001c0001t0003g0175 others(17): Show |
20 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.2541+999G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39253451 | |||||||
| chr2:39253537 | T | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2541+913A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39253537 | |||||||
| chr2:39253613 | G | C | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.2541+837C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39253613 | |||||||
| chr2:39253966 | G | T | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.2541+484C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39253966 | |||||||
| chr2:39254272 | G | C | 2 | a0001c0002t0001g0144 a0001c0002t0001g0193 |
2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.2541+178C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39254272 | |||||||
| chr2:39254387 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2541+63G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 32/33 | chr2 | 39254387 | |||||||
| chr2:39254733 | T | C | 1 | a0001c0003t0002g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2471-213A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39254733 | |||||||
| chr2:39254743 | A | C | 3 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 |
3 | HG01109.hp2 HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2471-223T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39254743 | |||||||
| chr2:39254744 | G | GT | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2471-225dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39254744 | |||||||
| chr2:39254832 | G | A | 9 | a0001c0003t0004g0214 a0001c0003t0004g0216 a0001c0003t0004g0217 others(6): Show |
9 | HG00408.hp1 HG01934.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.2471-312C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39254832 | |||||||
| chr2:39254946 | T | C | 160 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(157): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.2471-426A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39254946 | |||||||
| chr2:39254987 | G | C | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2471-467C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39254987 | |||||||
| chr2:39255499 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2471-979G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39255499 | |||||||
| chr2:39255726 | A | G | 117 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0164 others(114): Show |
117 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.2471-1206T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39255726 | |||||||
| chr2:39255731 | G | A | 19 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(16): Show |
19 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.2471-1211C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39255731 | |||||||
| chr2:39255816 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2471-1296C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39255816 | |||||||
| chr2:39255928 | C | A | 9 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(6): Show |
9 | HG01496.hp1 HG02615.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.2471-1408G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39255928 | |||||||
| chr2:39256610 | G | A | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.2470+1738C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39256610 | |||||||
| chr2:39256628 | A | T | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2470+1720T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39256628 | |||||||
| chr2:39256742 | T | C | 18 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(15): Show |
18 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.2470+1606A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39256742 | |||||||
| chr2:39256806 | G | A | 150 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(147): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.2470+1542C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39256806 | |||||||
| chr2:39256848 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2470+1500A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39256848 | |||||||
| chr2:39257366 | T | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2470+982A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39257366 | |||||||
| chr2:39257570 | G | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2470+778C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39257570 | |||||||
| chr2:39257660 | G | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2470+688C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39257660 | |||||||
| chr2:39257680 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2470+668A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39257680 | |||||||
| chr2:39257796 | C | CA | 27 | a0001c0001t0003g0164 a0001c0001t0003g0166 a0001c0001t0003g0169 others(24): Show |
27 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.2470+551dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39257796 | |||||||
| chr2:39257821 | A | T | 24 | a0001c0001t0003g0164 a0001c0001t0003g0166 a0001c0001t0003g0169 others(21): Show |
24 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.2470+527T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39257821 | |||||||
| chr2:39257863 | T | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2470+485A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39257863 | |||||||
| chr2:39257994 | C | T | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2470+354G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39257994 | |||||||
| chr2:39258072 | C | T | 2 | a0001c0002t0007g0223 a0001c0002t0007g0230 |
2 | HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2470+276G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 31/33 | chr2 | 39258072 | |||||||
| chr2:39258471 | G | A | 24 | a0001c0001t0003g0164 a0001c0001t0003g0166 a0001c0001t0003g0169 others(21): Show |
24 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.2378-31C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 30/33 | chr2 | 39258471 | |||||||
| chr2:39258590 | A | G | 1 | a0001c0004t0005g0002 | 1 | HG02895.hp1 | splice_region_variant&intron_variant | LOW | c.2309-3T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39258590 | |||||||
| chr2:39258705 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2309-118A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39258705 | |||||||
| chr2:39258863 | A | G | 20 | a0001c0001t0003g0164 a0001c0001t0003g0166 a0001c0001t0003g0169 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2309-276T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39258863 | |||||||
| chr2:39258954 | A | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2309-367T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39258954 | |||||||
| chr2:39259008 | T | C | 16 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0154 others(13): Show |
16 | HG00738.hp2 HG01106.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.2309-421A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39259008 | |||||||
| chr2:39259010 | G | GTT | 83 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(80): Show |
83 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.2309-425_2309-424d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39259010 | |||||||
| chr2:39259010 | G | GTTT | 9 | a0001c0002t0001g0074 a0001c0002t0001g0113 a0001c0002t0001g0124 others(6): Show |
9 | HG01346.hp2 HG02055.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.2309-426_2309-424d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39259010 | |||||||
| chr2:39259405 | A | C | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2309-818T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39259405 | |||||||
| chr2:39259451 | G | T | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2309-864C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39259451 | |||||||
| chr2:39259475 | T | G | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2309-888A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39259475 | |||||||
| chr2:39259485 | A | G | 24 | a0001c0001t0003g0164 a0001c0001t0003g0166 a0001c0001t0003g0169 others(21): Show |
24 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.2309-898T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39259485 | |||||||
| chr2:39259571 | G | T | 1 | a0001c0001t0002g0171 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2309-984C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39259571 | |||||||
| chr2:39259586 | C | T | 91 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.2309-999G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39259586 | |||||||
| chr2:39259803 | T | C | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2308+803A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39259803 | |||||||
| chr2:39259932 | A | T | 91 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.2308+674T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39259932 | |||||||
| chr2:39259933 | C | T | 91 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.2308+673G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39259933 | |||||||
| chr2:39260208 | G | C | 1 | a0001c0003t0004g0227 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2308+398C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39260208 | |||||||
| chr2:39260289 | C | T | 175 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.2308+317G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39260289 | |||||||
| chr2:39260291 | A | AT | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.2308+314dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39260291 | |||||||
| chr2:39260314 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2308+292G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39260314 | |||||||
| chr2:39260392 | T | C | 175 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.2308+214A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 29/33 | chr2 | 39260392 | |||||||
| chr2:39261032 | C | G | 24 | a0001c0001t0003g0164 a0001c0001t0003g0166 a0001c0001t0003g0169 others(21): Show |
24 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.2137-255G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39261032 | |||||||
| chr2:39261197 | T | C | 1 | a0001c0002t0001g0037 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2137-420A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39261197 | |||||||
| chr2:39261230 | G | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2137-453C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39261230 | |||||||
| chr2:39261314 | A | G | 1 | a0001c0003t0007g0221 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2137-537T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39261314 | |||||||
| chr2:39261328 | T | TAA | 133 | a0001c0001t0001g0180 a0001c0001t0002g0052 a0001c0001t0002g0053 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2137-552_2137-551i others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39261328 | |||||||
| chr2:39261415 | C | A | 1 | a0001c0002t0001g0080 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2137-638G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39261415 | |||||||
| chr2:39261453 | C | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2137-676G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39261453 | |||||||
| chr2:39261612 | T | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2137-835A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39261612 | |||||||
| chr2:39261691 | T | G | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2137-914A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39261691 | |||||||
| chr2:39261694 | G | A | 1 | a0001c0001t0003g0174 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2137-917C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39261694 | |||||||
| chr2:39261909 | G | T | 21 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(18): Show |
21 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.2137-1132C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39261909 | |||||||
| chr2:39262176 | A | C | 1 | a0001c0002t0001g0083 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2137-1399T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39262176 | |||||||
| chr2:39262222 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2137-1445A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39262222 | |||||||
| chr2:39262297 | T | C | 133 | a0001c0001t0001g0180 a0001c0001t0002g0052 a0001c0001t0002g0053 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2137-1520A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39262297 | |||||||
| chr2:39262498 | A | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2137-1721T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39262498 | |||||||
| chr2:39262559 | C | T | 25 | a0001c0001t0003g0032 a0001c0001t0003g0164 a0001c0001t0003g0166 others(22): Show |
25 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2137-1782G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39262559 | |||||||
| chr2:39262562 | T | A | 4 | a0001c0001t0003g0164 a0001c0001t0003g0166 a0001c0001t0003g0169 others(1): Show |
4 | HG02717.hp2 HG03209.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-1785A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39262562 | |||||||
| chr2:39262710 | T | C | 7 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(4): Show |
7 | HG01496.hp1 HG03195.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2137-1933A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39262710 | |||||||
| chr2:39262727 | A | G | 1 | a0001c0001t0002g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2137-1950T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39262727 | |||||||
| chr2:39262874 | G | A | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2137-2097C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39262874 | |||||||
| chr2:39262903 | G | A | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2137-2126C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39262903 | |||||||
| chr2:39263002 | G | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2136+2201C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263002 | |||||||
| chr2:39263087 | A | G | 2 | a0001c0002t0001g0112 a0001c0002t0001g0115 |
2 | HG03017.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2136+2116T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263087 | |||||||
| chr2:39263250 | G | C | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.2136+1953C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263250 | |||||||
| chr2:39263272 | G | GT | 24 | a0001c0001t0001g0180 a0001c0001t0002g0020 a0001c0001t0002g0021 others(21): Show |
24 | HG00741.hp2 HG01358.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.2136+1930dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263272 | |||||||
| chr2:39263304 | G | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2136+1899C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263304 | |||||||
| chr2:39263311 | G | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2136+1892C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263311 | |||||||
| chr2:39263438 | A | AT | 42 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(39): Show |
42 | HG01099.hp2 HG01243.hp2 HG01433.hp2 others(39): Show |
intron_variant | MODIFIER | c.2136+1764dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263438 | |||||||
| chr2:39263438 | A | ATT | 131 | a0001c0001t0001g0180 a0001c0001t0002g0052 a0001c0001t0002g0053 others(128): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.2136+1763_2136+176 others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263438 | |||||||
| chr2:39263454 | T | C | 1 | a0001c0002t0001g0066 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2136+1749A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263454 | |||||||
| chr2:39263507 | C | T | 7 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(4): Show |
7 | HG01496.hp1 HG03195.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2136+1696G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263507 | |||||||
| chr2:39263515 | G | A | 1 | a0001c0001t0002g0053 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2136+1688C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263515 | |||||||
| chr2:39263526 | G | A | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2136+1677C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263526 | |||||||
| chr2:39263530 | C | T | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+1673G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263530 | |||||||
| chr2:39263551 | T | A | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2136+1652A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263551 | |||||||
| chr2:39263636 | A | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2136+1567T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263636 | |||||||
| chr2:39263722 | T | C | 34 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(31): Show |
34 | HG01099.hp2 HG01243.hp2 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.2136+1481A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263722 | |||||||
| chr2:39263835 | G | A | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+1368C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263835 | |||||||
| chr2:39263888 | T | C | 25 | a0001c0001t0003g0032 a0001c0001t0003g0164 a0001c0001t0003g0166 others(22): Show |
25 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2136+1315A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263888 | |||||||
| chr2:39263997 | C | T | 1 | a0001c0001t0005g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2136+1206G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39263997 | |||||||
| chr2:39264027 | A | C | 1 | a0001c0001t0002g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2136+1176T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39264027 | |||||||
| chr2:39264093 | G | A | 1 | a0001c0002t0001g0196 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2136+1110C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39264093 | |||||||
| chr2:39264396 | C | T | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2136+807G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39264396 | |||||||
| chr2:39264401 | G | T | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2136+802C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39264401 | |||||||
| chr2:39264651 | T | C | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2136+552A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39264651 | |||||||
| chr2:39264689 | T | G | 1 | a0001c0001t0005g0015 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2136+514A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39264689 | |||||||
| chr2:39264691 | A | G | 1 | a0001c0001t0005g0015 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2136+512T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39264691 | |||||||
| chr2:39264833 | C | T | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2136+370G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39264833 | |||||||
| chr2:39264887 | G | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2136+316C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39264887 | |||||||
| chr2:39264930 | T | C | 10 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2136+273A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39264930 | |||||||
| chr2:39264931 | A | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2136+272T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39264931 | |||||||
| chr2:39264961 | T | C | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2136+242A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39264961 | |||||||
| chr2:39265003 | C | A | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.2136+200G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 28/33 | chr2 | 39265003 | |||||||
| chr2:39265322 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2033-16A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39265322 | |||||||
| chr2:39265462 | G | A | 1 | a0001c0001t0005g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2033-156C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39265462 | |||||||
| chr2:39265529 | C | T | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2033-223G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39265529 | |||||||
| chr2:39265590 | T | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2033-284A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39265590 | |||||||
| chr2:39265650 | G | T | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2033-344C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39265650 | |||||||
| chr2:39265716 | A | T | 1 | a0001c0002t0001g0073 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2033-410T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39265716 | |||||||
| chr2:39265745 | G | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2033-439C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39265745 | |||||||
| chr2:39265796 | A | T | 1 | a0001c0001t0005g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2033-490T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39265796 | |||||||
| chr2:39265892 | T | C | 24 | a0001c0001t0003g0032 a0001c0001t0003g0173 a0001c0001t0003g0174 others(21): Show |
24 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.2033-586A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39265892 | |||||||
| chr2:39266004 | A | G | 1 | a0001c0002t0001g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2033-698T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266004 | |||||||
| chr2:39266041 | A | C | 1 | a0001c0001t0002g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2033-735T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266041 | |||||||
| chr2:39266144 | A | C | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.2033-838T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266144 | |||||||
| chr2:39266180 | T | C | 22 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0046 others(19): Show |
22 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2033-874A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266180 | |||||||
| chr2:39266222 | C | G | 3 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 |
3 | HG01109.hp2 HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2033-916G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266222 | |||||||
| chr2:39266300 | C | T | 1 | a0001c0002t0001g0138 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2032+889G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266300 | |||||||
| chr2:39266315 | T | C | 163 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(160): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.2032+874A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266315 | |||||||
| chr2:39266352 | C | A | 1 | a0001c0002t0001g0131 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2032+837G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266352 | |||||||
| chr2:39266461 | G | C | 1 | a0001c0002t0001g0144 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2032+728C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266461 | |||||||
| chr2:39266462 | C | T | 1 | a0001c0004t0013g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2032+727G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266462 | |||||||
| chr2:39266491 | T | C | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.2032+698A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266491 | |||||||
| chr2:39266544 | CTCTCCAT others(4): Show |
C | 2 | a0001c0001t0003g0190 a0001c0001t0014g0189 |
2 | HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2032+634_2032+644d others(13): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266544 | |||||||
| chr2:39266653 | G | C | 1 | a0001c0001t0003g0174 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2032+536C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266653 | |||||||
| chr2:39266806 | A | G | 1 | a0001c0001t0005g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2032+383T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266806 | |||||||
| chr2:39266852 | A | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2032+337T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266852 | |||||||
| chr2:39266907 | T | TA | 91 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.2032+281dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266907 | |||||||
| chr2:39266907 | TA | T | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2032+281delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39266907 | |||||||
| chr2:39267056 | C | T | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2032+133G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39267056 | |||||||
| chr2:39267087 | A | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2032+102T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39267087 | |||||||
| chr2:39267141 | T | A | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2032+48A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 27/33 | chr2 | 39267141 | |||||||
| chr2:39267328 | C | G | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1974-81G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39267328 | |||||||
| chr2:39267364 | C | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1974-117G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39267364 | |||||||
| chr2:39267425 | C | A | 91 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1974-178G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39267425 | |||||||
| chr2:39267455 | A | G | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1974-208T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39267455 | |||||||
| chr2:39267466 | T | C | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1974-219A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39267466 | |||||||
| chr2:39267484 | A | C | 91 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1974-237T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39267484 | |||||||
| chr2:39267535 | T | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1974-288A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39267535 | |||||||
| chr2:39267543 | T | C | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1974-296A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39267543 | |||||||
| chr2:39267679 | CA | C | 11 | a0001c0001t0003g0173 a0001c0001t0003g0179 a0001c0001t0003g0181 others(8): Show |
11 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1974-433delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39267679 | |||||||
| chr2:39267679 | CAA | C | 158 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(155): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1974-434_1974-433d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39267679 | |||||||
| chr2:39267777 | T | C | 1 | a0001c0001t0002g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1974-530A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39267777 | |||||||
| chr2:39267890 | T | C | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1974-643A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39267890 | |||||||
| chr2:39268020 | T | C | 1 | a0001c0002t0001g0196 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1974-773A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268020 | |||||||
| chr2:39268063 | T | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1974-816A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268063 | |||||||
| chr2:39268192 | A | T | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1974-945T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268192 | |||||||
| chr2:39268256 | T | C | 112 | a0001c0001t0001g0180 a0001c0001t0002g0052 a0001c0001t0002g0053 others(109): Show |
112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1974-1009A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268256 | |||||||
| chr2:39268260 | T | C | 5 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(2): Show |
5 | HG01496.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1974-1013A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268260 | |||||||
| chr2:39268351 | C | T | 1 | a0001c0001t0014g0189 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1974-1104G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268351 | |||||||
| chr2:39268359 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1974-1112G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268359 | |||||||
| chr2:39268366 | G | A | 1 | a0001c0003t0004g0227 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1974-1119C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268366 | |||||||
| chr2:39268634 | A | AT | 11 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(8): Show |
11 | HG00741.hp1 HG01496.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1974-1388dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268634 | |||||||
| chr2:39268634 | A | ATT | 19 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0052 others(16): Show |
19 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1974-1389_1974-138 others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268634 | |||||||
| chr2:39268634 | A | ATTTTT | 18 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0058 others(15): Show |
18 | HG00280.hp2 HG00741.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1974-1392_1974-138 others(9): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268634 | |||||||
| chr2:39268634 | A | ATTTTTT | 50 | a0001c0002t0001g0037 a0001c0002t0001g0038 a0001c0002t0001g0039 others(47): Show |
50 | HG00140.hp2 HG00609.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.1974-1393_1974-138 others(10): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268634 | |||||||
| chr2:39268634 | A | ATTTTTTT | 22 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0040 others(19): Show |
22 | HG00408.hp2 HG01106.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1974-1394_1974-138 others(11): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268634 | |||||||
| chr2:39268698 | G | C | 1 | a0004c0006t0004g0220 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1974-1451C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268698 | |||||||
| chr2:39268728 | C | T | 3 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 |
3 | HG01109.hp2 HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1974-1481G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268728 | |||||||
| chr2:39268743 | G | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1974-1496C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268743 | |||||||
| chr2:39268904 | C | T | 3 | a0001c0002t0001g0062 a0001c0002t0001g0065 a0001c0002t0001g0067 |
3 | NA18973.hp2 NA18982.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1974-1657G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268904 | |||||||
| chr2:39268913 | T | A | 1 | a0001c0001t0006g0199 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1974-1666A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39268913 | |||||||
| chr2:39269112 | CT | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1974-1866delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269112 | |||||||
| chr2:39269112 | CTT | C | 117 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(114): Show |
117 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1974-1867_1974-186 others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269112 | |||||||
| chr2:39269282 | C | T | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1974-2035G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269282 | |||||||
| chr2:39269297 | T | G | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1974-2050A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269297 | |||||||
| chr2:39269465 | C | T | 19 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(16): Show |
19 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1974-2218G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269465 | |||||||
| chr2:39269470 | C | CT | 39 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0027 others(36): Show |
39 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1974-2224dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269470 | |||||||
| chr2:39269470 | C | CTT | 87 | a0001c0001t0001g0180 a0001c0001t0002g0157 a0001c0001t0002g0165 others(84): Show |
87 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1974-2225_1974-222 others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269470 | |||||||
| chr2:39269470 | C | CTTT | 15 | a0001c0001t0002g0036 a0001c0001t0002g0167 a0001c0001t0002g0168 others(12): Show |
15 | HG01099.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1974-2226_1974-222 others(7): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269470 | |||||||
| chr2:39269470 | C | CTTTT | 20 | a0001c0001t0003g0032 a0001c0001t0003g0173 a0001c0001t0003g0174 others(17): Show |
20 | HG00609.hp2 HG01243.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-2227_1974-222 others(8): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269470 | |||||||
| chr2:39269579 | A | C | 1 | a0001c0003t0004g0227 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1974-2332T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269579 | |||||||
| chr2:39269634 | T | C | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1974-2387A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269634 | |||||||
| chr2:39269650 | T | A | 1 | a0001c0001t0005g0015 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1974-2403A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269650 | |||||||
| chr2:39269689 | A | G | 92 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1974-2442T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269689 | |||||||
| chr2:39269824 | AACACCTC others(3): Show |
A | 1 | a0001c0007t0001g0048 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1973+2449_1973+245 others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269824 | |||||||
| chr2:39269875 | A | G | 1 | a0001c0002t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1973+2408T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269875 | |||||||
| chr2:39269883 | C | A | 15 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(12): Show |
15 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1973+2400G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269883 | |||||||
| chr2:39269968 | G | A | 1 | a0001c0001t0002g0025 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1973+2315C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39269968 | |||||||
| chr2:39270063 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1973+2220G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39270063 | |||||||
| chr2:39270177 | T | G | 119 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(116): Show |
119 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1973+2106A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39270177 | |||||||
| chr2:39270208 | T | C | 25 | a0001c0001t0003g0032 a0001c0001t0003g0173 a0001c0001t0003g0174 others(22): Show |
25 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1973+2075A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39270208 | |||||||
| chr2:39270413 | A | G | 123 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0164 others(120): Show |
123 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1973+1870T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39270413 | |||||||
| chr2:39270617 | C | T | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1973+1666G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39270617 | |||||||
| chr2:39270717 | T | A | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1973+1566A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39270717 | |||||||
| chr2:39270823 | T | C | 1 | a0003c0009t0005g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1973+1460A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39270823 | |||||||
| chr2:39270911 | T | C | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1973+1372A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39270911 | |||||||
| chr2:39270961 | A | G | 1 | a0001c0002t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1973+1322T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39270961 | |||||||
| chr2:39271075 | T | C | 1 | a0001c0001t0005g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1973+1208A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39271075 | |||||||
| chr2:39271121 | A | G | 1 | a0001c0001t0002g0116 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1973+1162T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39271121 | |||||||
| chr2:39271185 | C | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1973+1098G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39271185 | |||||||
| chr2:39271250 | C | T | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1973+1033G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39271250 | |||||||
| chr2:39271316 | C | T | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1973+967G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39271316 | |||||||
| chr2:39271321 | A | G | 15 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(12): Show |
15 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1973+962T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39271321 | |||||||
| chr2:39271654 | T | C | 94 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(91): Show |
94 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1973+629A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39271654 | |||||||
| chr2:39271843 | T | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1973+440A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39271843 | |||||||
| chr2:39271872 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1973+411G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39271872 | |||||||
| chr2:39271923 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1973+360A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39271923 | |||||||
| chr2:39271977 | G | A | 1 | a0001c0001t0002g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1973+306C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39271977 | |||||||
| chr2:39272057 | G | A | 1 | a0001c0001t0003g0174 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1973+226C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39272057 | |||||||
| chr2:39272125 | A | C | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1973+158T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39272125 | |||||||
| chr2:39272264 | T | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1973+19A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 26/33 | chr2 | 39272264 | |||||||
| chr2:39272473 | T | A | 30 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(27): Show |
30 | HG00140.hp1 HG00408.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1855+9A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 25/33 | chr2 | 39272473 | |||||||
| chr2:39272655 | A | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1795-113T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39272655 | |||||||
| chr2:39272834 | A | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1795-292T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39272834 | |||||||
| chr2:39272841 | CA | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1795-300delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39272841 | |||||||
| chr2:39272876 | T | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1795-334A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39272876 | |||||||
| chr2:39272926 | C | T | 145 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(142): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1795-384G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39272926 | |||||||
| chr2:39273020 | G | T | 1 | a0001c0001t0002g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1795-478C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39273020 | |||||||
| chr2:39273180 | A | C | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1795-638T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39273180 | |||||||
| chr2:39273236 | T | C | 24 | a0001c0001t0003g0032 a0001c0001t0003g0173 a0001c0001t0003g0174 others(21): Show |
24 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1795-694A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39273236 | |||||||
| chr2:39273528 | A | G | 3 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 |
3 | HG01109.hp2 HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1795-986T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39273528 | |||||||
| chr2:39273536 | CA | C | 91 | a0001c0001t0001g0180 a0001c0002t0001g0026 a0001c0002t0001g0037 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1795-995delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39273536 | |||||||
| chr2:39273554 | C | T | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1795-1012G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39273554 | |||||||
| chr2:39273591 | A | G | 15 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(12): Show |
15 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1795-1049T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39273591 | |||||||
| chr2:39273666 | T | G | 28 | a0001c0001t0003g0032 a0001c0001t0003g0164 a0001c0001t0003g0166 others(25): Show |
28 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1795-1124A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39273666 | |||||||
| chr2:39273701 | T | A | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1795-1159A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39273701 | |||||||
| chr2:39273875 | C | G | 4 | a0001c0001t0002g0101 a0001c0001t0002g0104 a0001c0001t0002g0108 others(1): Show |
4 | HG00609.hp1 NA18995.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1795-1333G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39273875 | |||||||
| chr2:39273930 | CAGTACGT others(8): Show |
C | 15 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(12): Show |
15 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1795-1403_1795-138 others(19): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39273930 | |||||||
| chr2:39274038 | T | C | 1 | a0001c0001t0002g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1795-1496A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39274038 | |||||||
| chr2:39274108 | C | T | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1795-1566G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39274108 | |||||||
| chr2:39274221 | C | T | 170 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(167): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1795-1679G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39274221 | |||||||
| chr2:39274236 | A | C | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1795-1694T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39274236 | |||||||
| chr2:39274248 | G | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1795-1706C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39274248 | |||||||
| chr2:39274276 | G | A | 1 | a0001c0001t0002g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1795-1734C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39274276 | |||||||
| chr2:39274277 | C | T | 18 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(15): Show |
18 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1795-1735G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39274277 | |||||||
| chr2:39274318 | G | A | 24 | a0001c0001t0003g0173 a0001c0001t0003g0174 a0001c0001t0003g0175 others(21): Show |
24 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1795-1776C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39274318 | |||||||
| chr2:39274321 | C | A | 17 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(14): Show |
17 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1795-1779G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39274321 | |||||||
| chr2:39274418 | C | G | 1 | a0001c0001t0002g0135 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1795-1876G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39274418 | |||||||
| chr2:39274587 | T | C | 1 | a0001c0001t0002g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1795-2045A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39274587 | |||||||
| chr2:39274710 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1795-2168C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39274710 | |||||||
| chr2:39274922 | C | A | 2 | a0001c0001t0002g0116 a0001c0001t0002g0136 |
2 | NA18948.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1795-2380G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39274922 | |||||||
| chr2:39274945 | G | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1795-2403C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39274945 | |||||||
| chr2:39275004 | G | C | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1795-2462C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39275004 | |||||||
| chr2:39275348 | T | C | 3 | a0001c0002t0001g0131 a0001c0002t0001g0132 a0001c0002t0001g0151 |
3 | HG03831.hp1 HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1795-2806A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39275348 | |||||||
| chr2:39275377 | T | G | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1795-2835A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39275377 | |||||||
| chr2:39275384 | G | A | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1795-2842C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39275384 | |||||||
| chr2:39275757 | C | A | 1 | a0001c0002t0001g0146 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1794+2650G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39275757 | |||||||
| chr2:39275921 | G | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1794+2486C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39275921 | |||||||
| chr2:39276079 | G | A | 1 | a0001c0002t0001g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1794+2328C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276079 | |||||||
| chr2:39276092 | C | T | 1 | a0001c0002t0009g0129 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1794+2315G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276092 | |||||||
| chr2:39276167 | C | T | 16 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(13): Show |
16 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1794+2240G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276167 | |||||||
| chr2:39276209 | C | G | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1794+2198G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276209 | |||||||
| chr2:39276259 | T | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1794+2148A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276259 | |||||||
| chr2:39276269 | A | T | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1794+2138T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276269 | |||||||
| chr2:39276550 | A | G | 173 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(170): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1794+1857T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276550 | |||||||
| chr2:39276580 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1794+1827G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276580 | |||||||
| chr2:39276599 | T | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1794+1808A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276599 | |||||||
| chr2:39276683 | T | C | 2 | a0001c0002t0001g0144 a0001c0002t0001g0193 |
2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1794+1724A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276683 | |||||||
| chr2:39276695 | T | C | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1794+1712A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276695 | |||||||
| chr2:39276775 | G | A | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1794+1632C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276775 | |||||||
| chr2:39276786 | A | G | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1794+1621T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276786 | |||||||
| chr2:39276841 | G | A | 6 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0128 others(3): Show |
6 | HG01168.hp2 HG01169.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1794+1566C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276841 | |||||||
| chr2:39276880 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1794+1527G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276880 | |||||||
| chr2:39276942 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1794+1465G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276942 | |||||||
| chr2:39276949 | C | T | 2 | a0001c0002t0001g0074 a0001c0002t0001g0125 |
2 | HG01934.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1794+1458G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39276949 | |||||||
| chr2:39277021 | A | T | 1 | a0001c0001t0002g0054 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1794+1386T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39277021 | |||||||
| chr2:39277068 | T | C | 1 | a0001c0002t0001g0081 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1794+1339A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39277068 | |||||||
| chr2:39277125 | T | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1794+1282A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39277125 | |||||||
| chr2:39277137 | T | C | 1 | a0001c0003t0004g0227 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1794+1270A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39277137 | |||||||
| chr2:39277196 | T | C | 92 | a0001c0001t0003g0032 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1794+1211A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39277196 | |||||||
| chr2:39277219 | A | G | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1794+1188T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39277219 | |||||||
| chr2:39277230 | T | C | 2 | a0001c0001t0002g0107 a0001c0001t0002g0135 |
2 | HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1794+1177A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39277230 | |||||||
| chr2:39277513 | A | G | 22 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0046 others(19): Show |
22 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1794+894T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39277513 | |||||||
| chr2:39277599 | T | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1794+808A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39277599 | |||||||
| chr2:39277638 | C | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1794+769G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39277638 | |||||||
| chr2:39277657 | C | A | 1 | a0001c0001t0002g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1794+750G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39277657 | |||||||
| chr2:39277696 | T | C | 2 | a0001c0001t0002g0028 a0001c0001t0003g0032 |
2 | HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1794+711A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39277696 | |||||||
| chr2:39277737 | A | G | 2 | a0001c0003t0011g0001 a0001c0003t0012g0004 |
2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1794+670T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39277737 | |||||||
| chr2:39277990 | C | T | 2 | a0001c0001t0002g0140 a0001c0001t0002g0141 |
2 | NA18945.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.1794+417G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39277990 | |||||||
| chr2:39278047 | C | T | 1 | a0001c0002t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1794+360G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39278047 | |||||||
| chr2:39278091 | G | A | 1 | a0003c0009t0005g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1794+316C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39278091 | |||||||
| chr2:39278159 | C | G | 91 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1794+248G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39278159 | |||||||
| chr2:39278162 | C | A | 91 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1794+245G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39278162 | |||||||
| chr2:39278165 | C | A | 7 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0071 others(4): Show |
7 | HG01168.hp2 HG01169.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1794+242G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39278165 | |||||||
| chr2:39278176 | G | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1794+231C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39278176 | |||||||
| chr2:39278208 | G | C | 1 | a0001c0002t0001g0151 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1794+199C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39278208 | |||||||
| chr2:39278220 | C | A | 1 | a0001c0002t0001g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1794+187G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39278220 | |||||||
| chr2:39278300 | A | G | 1 | a0001c0001t0002g0135 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1794+107T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 24/33 | chr2 | 39278300 | |||||||
| chr2:39278600 | T | G | 1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1715-114A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39278600 | |||||||
| chr2:39278613 | G | C | 1 | a0001c0002t0009g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1715-127C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39278613 | |||||||
| chr2:39278749 | A | G | 184 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1715-263T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39278749 | |||||||
| chr2:39278768 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1715-282C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39278768 | |||||||
| chr2:39278784 | T | C | 7 | a0001c0001t0003g0173 a0001c0001t0003g0179 a0001c0001t0003g0181 others(4): Show |
7 | HG02055.hp2 HG02895.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1715-298A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39278784 | |||||||
| chr2:39278830 | A | G | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1715-344T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39278830 | |||||||
| chr2:39278850 | G | GAT | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1715-366_1715-365d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39278850 | |||||||
| chr2:39278875 | G | T | 2 | a0001c0001t0005g0015 a0003c0009t0005g0016 |
2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1715-389C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39278875 | |||||||
| chr2:39278933 | C | T | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1715-447G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39278933 | |||||||
| chr2:39279160 | G | T | 1 | a0001c0002t0001g0124 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1715-674C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39279160 | |||||||
| chr2:39279221 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1715-735A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39279221 | |||||||
| chr2:39279314 | C | T | 2 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
2 | HG01106.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1715-828G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39279314 | |||||||
| chr2:39279382 | T | C | 18 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(15): Show |
18 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1714+890A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39279382 | |||||||
| chr2:39279571 | G | T | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1714+701C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39279571 | |||||||
| chr2:39279615 | C | T | 28 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(25): Show |
28 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1714+657G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39279615 | |||||||
| chr2:39279866 | T | C | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1714+406A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39279866 | |||||||
| chr2:39280008 | T | C | 6 | a0001c0001t0005g0008 a0001c0001t0005g0009 a0001c0001t0005g0011 others(3): Show |
6 | HG02258.hp2 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1714+264A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39280008 | |||||||
| chr2:39280073 | G | C | 4 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0003g0184 others(1): Show |
4 | HG02109.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714+199C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39280073 | |||||||
| chr2:39280188 | A | T | 9 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(6): Show |
9 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1714+84T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 23/33 | chr2 | 39280188 | |||||||
| chr2:39280497 | A | T | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1630-141T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39280497 | |||||||
| chr2:39280768 | T | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1630-412A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39280768 | |||||||
| chr2:39280833 | T | C | 1 | a0001c0002t0001g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1630-477A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39280833 | |||||||
| chr2:39280980 | A | C | 91 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1630-624T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39280980 | |||||||
| chr2:39280983 | A | G | 1 | a0001c0002t0001g0074 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1630-627T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39280983 | |||||||
| chr2:39280987 | C | A | 28 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(25): Show |
28 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1630-631G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39280987 | |||||||
| chr2:39281090 | A | G | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1630-734T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39281090 | |||||||
| chr2:39281151 | G | A | 119 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(116): Show |
119 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1630-795C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39281151 | |||||||
| chr2:39281245 | C | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1630-889G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39281245 | |||||||
| chr2:39281380 | T | C | 6 | a0001c0001t0003g0173 a0001c0001t0003g0181 a0001c0001t0003g0186 others(3): Show |
6 | HG02055.hp2 HG02895.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1630-1024A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39281380 | |||||||
| chr2:39281577 | A | C | 30 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(27): Show |
30 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1629+936T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39281577 | |||||||
| chr2:39281689 | C | T | 37 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(34): Show |
37 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1629+824G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39281689 | |||||||
| chr2:39281795 | A | G | 10 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1629+718T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39281795 | |||||||
| chr2:39281959 | C | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1629+554G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39281959 | |||||||
| chr2:39282138 | T | C | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1629+375A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39282138 | |||||||
| chr2:39282194 | C | CA | 63 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(60): Show |
63 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.1629+318dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39282194 | |||||||
| chr2:39282216 | G | C | 8 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(5): Show |
8 | HG01496.hp1 HG02717.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1629+297C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39282216 | |||||||
| chr2:39282222 | G | C | 109 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(106): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1629+291C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39282222 | |||||||
| chr2:39282268 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1629+245A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39282268 | |||||||
| chr2:39282272 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1629+241G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39282272 | |||||||
| chr2:39282410 | A | G | 6 | a0001c0001t0003g0173 a0001c0001t0003g0181 a0001c0001t0003g0186 others(3): Show |
6 | HG02055.hp2 HG02895.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1629+103T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39282410 | |||||||
| chr2:39282460 | C | T | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1629+53G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 22/33 | chr2 | 39282460 | |||||||
| chr2:39282569 | C | T | 1 | a0001c0002t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1588-15G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39282569 | |||||||
| chr2:39282700 | T | C | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1588-146A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39282700 | |||||||
| chr2:39282780 | G | C | 90 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1588-226C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39282780 | |||||||
| chr2:39282818 | G | C | 39 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(36): Show |
39 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1588-264C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39282818 | |||||||
| chr2:39282820 | C | T | 1 | a0001c0001t0003g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1588-266G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39282820 | |||||||
| chr2:39282987 | G | C | 26 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(23): Show |
26 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1588-433C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39282987 | |||||||
| chr2:39283017 | C | G | 1 | a0001c0001t0002g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1588-463G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39283017 | |||||||
| chr2:39283219 | T | C | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1588-665A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39283219 | |||||||
| chr2:39283282 | G | A | 1 | a0001c0002t0001g0151 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1588-728C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39283282 | |||||||
| chr2:39283511 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1588-957A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39283511 | |||||||
| chr2:39283713 | C | G | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1588-1159G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39283713 | |||||||
| chr2:39283836 | G | A | 90 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1588-1282C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39283836 | |||||||
| chr2:39283853 | C | G | 1 | a0001c0002t0001g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1588-1299G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39283853 | |||||||
| chr2:39284157 | T | G | 91 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1588-1603A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284157 | |||||||
| chr2:39284240 | C | A | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1588-1686G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284240 | |||||||
| chr2:39284333 | G | C | 38 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(35): Show |
38 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1588-1779C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284333 | |||||||
| chr2:39284430 | G | A | 1 | a0001c0002t0001g0128 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1588-1876C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284430 | |||||||
| chr2:39284457 | G | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1588-1903C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284457 | |||||||
| chr2:39284519 | T | A | 1 | a0001c0002t0001g0151 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1588-1965A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284519 | |||||||
| chr2:39284572 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1588-2018C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284572 | |||||||
| chr2:39284618 | G | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1588-2064C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284618 | |||||||
| chr2:39284644 | G | A | 2 | a0001c0002t0009g0129 a0001c0008t0002g0088 |
2 | NA19012.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1588-2090C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284644 | |||||||
| chr2:39284673 | G | A | 1 | a0001c0002t0001g0128 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1588-2119C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284673 | |||||||
| chr2:39284759 | A | C | 1 | a0001c0001t0002g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1587+2093T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284759 | |||||||
| chr2:39284802 | C | T | 2 | a0001c0002t0001g0073 a0001c0002t0001g0120 |
2 | HG00140.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1587+2050G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284802 | |||||||
| chr2:39284813 | T | C | 30 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(27): Show |
30 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1587+2039A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284813 | |||||||
| chr2:39284885 | T | C | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1587+1967A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284885 | |||||||
| chr2:39284938 | T | C | 25 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(22): Show |
25 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1587+1914A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284938 | |||||||
| chr2:39284944 | G | A | 24 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(21): Show |
24 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1587+1908C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39284944 | |||||||
| chr2:39285283 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1587+1569A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39285283 | |||||||
| chr2:39285296 | T | C | 91 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1587+1556A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39285296 | |||||||
| chr2:39285369 | C | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1587+1483G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39285369 | |||||||
| chr2:39285372 | T | C | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1587+1480A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39285372 | |||||||
| chr2:39285596 | GAAT | G | 2 | a0001c0001t0002g0023 a0001c0002t0001g0111 |
2 | HG03540.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1587+1253_1587+125 others(7): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39285596 | |||||||
| chr2:39285640 | AAC | A | 28 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(25): Show |
28 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1587+1210_1587+121 others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39285640 | |||||||
| chr2:39285794 | T | C | 180 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(177): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1587+1058A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39285794 | |||||||
| chr2:39285804 | T | G | 1 | a0001c0002t0001g0080 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1587+1048A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39285804 | |||||||
| chr2:39285877 | G | C | 1 | a0001c0002t0001g0120 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1587+975C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39285877 | |||||||
| chr2:39285985 | T | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1587+867A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39285985 | |||||||
| chr2:39286107 | G | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1587+745C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39286107 | |||||||
| chr2:39286163 | A | G | 22 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0046 others(19): Show |
22 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1587+689T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39286163 | |||||||
| chr2:39286259 | A | G | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1587+593T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39286259 | |||||||
| chr2:39286541 | G | T | 1 | a0001c0001t0002g0054 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1587+311C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39286541 | |||||||
| chr2:39286554 | T | C | 147 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(144): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1587+298A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39286554 | |||||||
| chr2:39286587 | A | G | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1587+265T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39286587 | |||||||
| chr2:39286588 | A | G | 1 | a0001c0002t0001g0080 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1587+264T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 21/33 | chr2 | 39286588 | |||||||
| chr2:39286995 | T | C | 90 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1475-31A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39286995 | |||||||
| chr2:39287063 | G | C | 90 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1475-99C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39287063 | |||||||
| chr2:39287127 | A | G | 7 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(4): Show |
7 | HG02165.hp1 NA18953.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.1475-163T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39287127 | |||||||
| chr2:39287170 | C | A | 2 | a0001c0001t0002g0104 a0001c0001t0002g0108 |
2 | NA18995.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1475-206G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39287170 | |||||||
| chr2:39287298 | C | CT | 213 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(210): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1475-335dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39287298 | |||||||
| chr2:39287298 | C | CTT | 13 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(10): Show |
13 | HG01243.hp1 HG01496.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1475-336_1475-335d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39287298 | |||||||
| chr2:39287400 | C | T | 3 | a0001c0002t0001g0095 a0001c0002t0001g0096 a0001c0002t0001g0114 |
3 | HG00280.hp2 HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1475-436G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39287400 | |||||||
| chr2:39287427 | AGCTG | A | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1475-467_1475-464d others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39287427 | |||||||
| chr2:39287445 | G | A | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1475-481C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39287445 | |||||||
| chr2:39287491 | T | C | 183 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1475-527A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39287491 | |||||||
| chr2:39287492 | G | A | 10 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1475-528C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39287492 | |||||||
| chr2:39287509 | G | C | 6 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0128 others(3): Show |
6 | HG01168.hp2 HG01169.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1475-545C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39287509 | |||||||
| chr2:39287578 | C | T | 24 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(21): Show |
24 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1474+543G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39287578 | |||||||
| chr2:39287667 | T | C | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1474+454A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39287667 | |||||||
| chr2:39287806 | T | C | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0130 |
3 | NA18948.hp1 NA18960.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1474+315A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39287806 | |||||||
| chr2:39287876 | C | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1474+245G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39287876 | |||||||
| chr2:39288056 | A | C | 1 | a0001c0003t0002g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1474+65T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39288056 | |||||||
| chr2:39288110 | T | G | 2 | a0001c0003t0004g0225 a0001c0003t0004g0226 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1474+11A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 20/33 | chr2 | 39288110 | |||||||
| chr2:39288300 | G | A | 1 | a0001c0002t0007g0230 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1315-20C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39288300 | |||||||
| chr2:39288359 | G | C | 1 | a0001c0002t0001g0138 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1315-79C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39288359 | |||||||
| chr2:39288378 | T | C | 1 | a0001c0001t0002g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1315-98A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39288378 | |||||||
| chr2:39288454 | T | C | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1315-174A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39288454 | |||||||
| chr2:39288555 | C | G | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1315-275G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39288555 | |||||||
| chr2:39288775 | G | A | 1 | a0001c0002t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1315-495C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39288775 | |||||||
| chr2:39288817 | C | T | 2 | a0001c0002t0001g0060 a0001c0002t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1315-537G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39288817 | |||||||
| chr2:39288825 | A | G | 109 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(106): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1315-545T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39288825 | |||||||
| chr2:39288827 | C | G | 1 | a0001c0002t0001g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1315-547G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39288827 | |||||||
| chr2:39289009 | G | A | 4 | a0001c0002t0001g0134 a0001c0002t0001g0195 a0001c0002t0001g0196 others(1): Show |
4 | NA18986.hp2 NA19054.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.1315-729C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39289009 | |||||||
| chr2:39289050 | T | TCAAAA | 4 | a0001c0001t0003g0164 a0001c0001t0003g0166 a0001c0001t0003g0169 others(1): Show |
4 | HG02717.hp2 HG03209.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315-775_1315-771d others(7): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39289050 | |||||||
| chr2:39289168 | G | A | 17 | a0001c0003t0004g0214 a0001c0003t0004g0216 a0001c0003t0004g0217 others(14): Show |
17 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1315-888C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39289168 | |||||||
| chr2:39289214 | T | C | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1315-934A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39289214 | |||||||
| chr2:39289288 | T | C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1314+1004A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39289288 | |||||||
| chr2:39289382 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1314+910A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39289382 | |||||||
| chr2:39289418 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1314+874A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39289418 | |||||||
| chr2:39289433 | T | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1314+859A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39289433 | |||||||
| chr2:39289482 | A | T | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314+810T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39289482 | |||||||
| chr2:39289644 | T | C | 2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1314+648A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39289644 | |||||||
| chr2:39289665 | T | C | 1 | a0001c0002t0001g0038 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1314+627A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39289665 | |||||||
| chr2:39289793 | C | T | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314+499G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39289793 | |||||||
| chr2:39289872 | G | T | 2 | a0001c0001t0003g0182 a0001c0001t0003g0185 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1314+420C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39289872 | |||||||
| chr2:39289931 | C | T | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1314+361G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39289931 | |||||||
| chr2:39290084 | C | CAA | 8 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(5): Show |
8 | HG01496.hp1 HG02717.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1314+206_1314+207d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39290084 | |||||||
| chr2:39290084 | CA | C | 53 | a0001c0001t0002g0042 a0001c0001t0002g0045 a0001c0001t0002g0097 others(50): Show |
53 | HG00140.hp1 HG00408.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1314+207delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39290084 | |||||||
| chr2:39290084 | CAA | C | 53 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(50): Show |
53 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.1314+206_1314+207d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39290084 | |||||||
| chr2:39290084 | CAAA | C | 6 | a0001c0001t0003g0181 a0001c0001t0006g0198 a0001c0001t0006g0200 others(3): Show |
6 | HG01433.hp2 HG02976.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1314+205_1314+207d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39290084 | |||||||
| chr2:39290084 | CAAAAAAA others(1): Show |
C | 87 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(84): Show |
87 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1314+200_1314+207d others(10): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 19/33 | chr2 | 39290084 | |||||||
| chr2:39290402 | A | AT | 30 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(27): Show |
30 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1272-69dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39290402 | |||||||
| chr2:39290417 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1272-83G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39290417 | |||||||
| chr2:39290431 | A | G | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1272-97T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39290431 | |||||||
| chr2:39290521 | C | T | 8 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(5): Show |
8 | HG01496.hp1 HG02717.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272-187G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39290521 | |||||||
| chr2:39290577 | A | T | 110 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(107): Show |
110 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1272-243T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39290577 | |||||||
| chr2:39290593 | A | C | 110 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(107): Show |
110 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1272-259T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39290593 | |||||||
| chr2:39290675 | C | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1272-341G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39290675 | |||||||
| chr2:39290739 | T | C | 110 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(107): Show |
110 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1272-405A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39290739 | |||||||
| chr2:39290796 | C | A | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1272-462G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39290796 | |||||||
| chr2:39290845 | C | A | 1 | a0001c0002t0001g0149 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1272-511G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39290845 | |||||||
| chr2:39290852 | C | A | 7 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(4): Show |
7 | HG01496.hp1 HG03195.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1272-518G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39290852 | |||||||
| chr2:39290911 | T | C | 110 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(107): Show |
110 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1272-577A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39290911 | |||||||
| chr2:39290914 | TA | T | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272-581delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39290914 | |||||||
| chr2:39290948 | G | A | 1 | a0001c0008t0002g0088 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1272-614C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39290948 | |||||||
| chr2:39290978 | A | G | 110 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(107): Show |
110 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1272-644T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39290978 | |||||||
| chr2:39291013 | T | C | 110 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(107): Show |
110 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1272-679A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39291013 | |||||||
| chr2:39291171 | G | A | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1272-837C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39291171 | |||||||
| chr2:39291285 | T | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1272-951A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39291285 | |||||||
| chr2:39291308 | C | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1272-974G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39291308 | |||||||
| chr2:39291365 | T | C | 2 | a0001c0002t0001g0073 a0001c0002t0001g0120 |
2 | HG00140.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1272-1031A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39291365 | |||||||
| chr2:39291371 | T | G | 108 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(105): Show |
108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1272-1037A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39291371 | |||||||
| chr2:39291511 | A | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1272-1177T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39291511 | |||||||
| chr2:39291606 | C | A | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1271+1167G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39291606 | |||||||
| chr2:39291664 | T | C | 1 | a0001c0001t0003g0174 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1271+1109A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39291664 | |||||||
| chr2:39291707 | G | A | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1271+1066C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39291707 | |||||||
| chr2:39291714 | C | A | 1 | a0001c0002t0001g0040 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1271+1059G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39291714 | |||||||
| chr2:39291758 | T | G | 1 | a0001c0001t0005g0015 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1271+1015A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39291758 | |||||||
| chr2:39291956 | T | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1271+817A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39291956 | |||||||
| chr2:39292038 | TA | T | 16 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(13): Show |
16 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1271+734delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39292038 | |||||||
| chr2:39292399 | C | G | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1271+374G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39292399 | |||||||
| chr2:39292400 | G | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1271+373C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39292400 | |||||||
| chr2:39292437 | G | A | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1271+336C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39292437 | |||||||
| chr2:39292542 | T | A | 5 | a0001c0003t0004g0215 a0001c0003t0004g0225 a0001c0003t0004g0226 others(2): Show |
5 | HG03490.hp2 HG03492.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271+231A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39292542 | |||||||
| chr2:39292554 | G | C | 1 | a0001c0002t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1271+219C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39292554 | |||||||
| chr2:39292577 | T | C | 107 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(104): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1271+196A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39292577 | |||||||
| chr2:39292682 | T | C | 1 | a0001c0002t0010g0211 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1271+91A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39292682 | |||||||
| chr2:39292769 | T | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1271+4A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 18/33 | chr2 | 39292769 | |||||||
| chr2:39292960 | C | G | 1 | a0001c0001t0003g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1218-134G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 17/33 | chr2 | 39292960 | |||||||
| chr2:39293138 | C | T | 1 | a0001c0002t0001g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1217+92G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 17/33 | chr2 | 39293138 | |||||||
| chr2:39293422 | A | G | 18 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(15): Show |
18 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1179-154T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39293422 | |||||||
| chr2:39293532 | C | A | 1 | a0001c0002t0009g0129 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1179-264G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39293532 | |||||||
| chr2:39293613 | C | T | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1179-345G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39293613 | |||||||
| chr2:39293818 | C | A | 4 | a0001c0002t0001g0145 a0001c0002t0001g0146 a0001c0002t0001g0147 others(1): Show |
4 | HG00741.hp2 HG01168.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179-550G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39293818 | |||||||
| chr2:39294034 | T | C | 1 | a0001c0001t0005g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1179-766A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39294034 | |||||||
| chr2:39294072 | T | C | 1 | a0001c0001t0005g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1179-804A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39294072 | |||||||
| chr2:39294114 | A | G | 31 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(28): Show |
31 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1179-846T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39294114 | |||||||
| chr2:39294249 | G | C | 3 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0055 |
3 | NA18998.hp2 NA19012.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1179-981C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39294249 | |||||||
| chr2:39294423 | T | C | 1 | a0001c0002t0001g0080 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1179-1155A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39294423 | |||||||
| chr2:39294451 | T | C | 4 | a0001c0002t0001g0095 a0001c0002t0001g0096 a0001c0002t0001g0113 others(1): Show |
4 | HG00280.hp2 HG01109.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179-1183A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39294451 | |||||||
| chr2:39294502 | A | G | 18 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(15): Show |
18 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1179-1234T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39294502 | |||||||
| chr2:39294576 | T | C | 18 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(15): Show |
18 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1179-1308A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39294576 | |||||||
| chr2:39294592 | G | C | 1 | a0001c0005t0002g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1179-1324C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39294592 | |||||||
| chr2:39294610 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1179-1342C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39294610 | |||||||
| chr2:39294713 | G | A | 90 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1179-1445C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39294713 | |||||||
| chr2:39294976 | G | A | 18 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(15): Show |
18 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1179-1708C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39294976 | |||||||
| chr2:39295006 | G | C | 28 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(25): Show |
28 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1179-1738C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295006 | |||||||
| chr2:39295099 | A | T | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1179-1831T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295099 | |||||||
| chr2:39295104 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1179-1836A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295104 | |||||||
| chr2:39295220 | G | C | 1 | a0001c0002t0001g0080 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1179-1952C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295220 | |||||||
| chr2:39295307 | A | C | 105 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(102): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1179-2039T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295307 | |||||||
| chr2:39295509 | A | G | 1 | a0001c0001t0005g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1179-2241T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295509 | |||||||
| chr2:39295542 | G | C | 2 | a0001c0002t0001g0069 a0001c0002t0001g0094 |
2 | NA18954.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1179-2274C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295542 | |||||||
| chr2:39295590 | T | A | 30 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(27): Show |
30 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1179-2322A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295590 | |||||||
| chr2:39295701 | C | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1179-2433G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295701 | |||||||
| chr2:39295715 | G | GT | 28 | a0001c0001t0001g0180 a0001c0001t0002g0106 a0001c0001t0002g0118 others(25): Show |
28 | HG00738.hp2 HG01099.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.1179-2448dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295715 | |||||||
| chr2:39295715 | GT | G | 85 | a0001c0001t0015g0192 a0001c0002t0001g0026 a0001c0002t0001g0037 others(82): Show |
85 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1179-2448delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295715 | |||||||
| chr2:39295719 | T | G | 6 | a0001c0001t0005g0008 a0001c0001t0005g0009 a0001c0001t0005g0011 others(3): Show |
6 | HG02258.hp2 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1179-2451A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295719 | |||||||
| chr2:39295764 | T | G | 2 | a0001c0003t0012g0004 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1179-2496A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295764 | |||||||
| chr2:39295779 | C | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1179-2511G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295779 | |||||||
| chr2:39295873 | C | G | 88 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(85): Show |
88 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1179-2605G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295873 | |||||||
| chr2:39295879 | C | T | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1179-2611G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295879 | |||||||
| chr2:39295922 | T | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1179-2654A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295922 | |||||||
| chr2:39295949 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1179-2681G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295949 | |||||||
| chr2:39295952 | C | T | 1 | a0001c0008t0002g0088 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1179-2684G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39295952 | |||||||
| chr2:39296004 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1179-2736C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39296004 | |||||||
| chr2:39296133 | T | A | 1 | a0001c0002t0001g0080 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1179-2865A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39296133 | |||||||
| chr2:39296210 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1179-2942G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39296210 | |||||||
| chr2:39296291 | A | G | 22 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1179-3023T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39296291 | |||||||
| chr2:39296533 | A | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1178+3210T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39296533 | |||||||
| chr2:39296583 | C | T | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1178+3160G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39296583 | |||||||
| chr2:39296606 | A | G | 2 | a0001c0003t0012g0004 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1178+3137T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39296606 | |||||||
| chr2:39296688 | A | C | 2 | a0001c0002t0001g0131 a0001c0002t0001g0132 |
2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1178+3055T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39296688 | |||||||
| chr2:39296702 | CA | C | 3 | a0001c0001t0003g0173 a0001c0001t0003g0181 a0001c0001t0003g0186 |
3 | HG02055.hp2 HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1178+3040delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39296702 | |||||||
| chr2:39296856 | T | G | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1178+2887A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39296856 | |||||||
| chr2:39296958 | C | T | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1178+2785G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39296958 | |||||||
| chr2:39297092 | C | A | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1178+2651G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39297092 | |||||||
| chr2:39297186 | C | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1178+2557G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39297186 | |||||||
| chr2:39297220 | C | A | 1 | a0001c0002t0001g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1178+2523G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39297220 | |||||||
| chr2:39297262 | C | T | 1 | a0001c0002t0001g0058 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1178+2481G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39297262 | |||||||
| chr2:39297598 | C | T | 169 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(166): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.1178+2145G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39297598 | |||||||
| chr2:39297832 | C | T | 3 | a0001c0003t0011g0001 a0001c0003t0012g0004 a0002c0010t0005g0017 |
3 | HG02615.hp1 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1178+1911G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39297832 | |||||||
| chr2:39297961 | G | A | 9 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(6): Show |
9 | HG01433.hp2 NA18942.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1178+1782C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39297961 | |||||||
| chr2:39298350 | T | A | 2 | a0001c0002t0001g0060 a0001c0002t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1178+1393A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39298350 | |||||||
| chr2:39298427 | A | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1178+1316T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39298427 | |||||||
| chr2:39298657 | C | A | 19 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(16): Show |
19 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1178+1086G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39298657 | |||||||
| chr2:39298797 | C | T | 1 | a0001c0002t0001g0085 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1178+946G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39298797 | |||||||
| chr2:39298964 | C | CA | 32 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(29): Show |
32 | HG00609.hp1 HG01243.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.1178+778dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39298964 | |||||||
| chr2:39298964 | C | CAA | 12 | a0001c0001t0002g0029 a0001c0001t0002g0035 a0001c0001t0003g0194 others(9): Show |
12 | HG01433.hp2 HG01496.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1178+777_1178+778d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39298964 | |||||||
| chr2:39298982 | A | AC | 13 | a0001c0003t0004g0214 a0001c0003t0004g0216 a0001c0003t0004g0218 others(10): Show |
13 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.1178+760_1178+761i others(3): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39298982 | |||||||
| chr2:39299246 | A | G | 1 | a0001c0001t0003g0190 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1178+497T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39299246 | |||||||
| chr2:39299253 | T | C | 1 | a0001c0001t0002g0020 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1178+490A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39299253 | |||||||
| chr2:39299276 | T | G | 93 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(90): Show |
93 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1178+467A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39299276 | |||||||
| chr2:39299352 | G | T | 8 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(5): Show |
8 | HG01496.hp1 HG02717.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1178+391C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39299352 | |||||||
| chr2:39299353 | A | G | 8 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(5): Show |
8 | HG01496.hp1 HG02717.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1178+390T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39299353 | |||||||
| chr2:39299428 | A | G | 8 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(5): Show |
8 | HG01496.hp1 HG02717.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1178+315T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39299428 | |||||||
| chr2:39299701 | A | C | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1178+42T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 16/33 | chr2 | 39299701 | |||||||
| chr2:39299806 | T | C | 9 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(6): Show |
9 | HG01433.hp2 NA18942.hp2 NA18945.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.1120-5A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39299806 | |||||||
| chr2:39300052 | TTTAA | T | 9 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(6): Show |
9 | HG01433.hp2 NA18942.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1120-255_1120-252d others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39300052 | |||||||
| chr2:39300122 | A | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1120-321T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39300122 | |||||||
| chr2:39300268 | G | A | 169 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(166): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.1120-467C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39300268 | |||||||
| chr2:39300298 | C | T | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1120-497G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39300298 | |||||||
| chr2:39300550 | T | C | 1 | a0001c0001t0002g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1120-749A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39300550 | |||||||
| chr2:39300631 | T | C | 1 | a0001c0001t0002g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1120-830A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39300631 | |||||||
| chr2:39300721 | C | T | 90 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1120-920G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39300721 | |||||||
| chr2:39300801 | C | T | 3 | a0001c0002t0010g0210 a0001c0002t0010g0211 a0001c0002t0010g0213 |
3 | HG02165.hp2 HG03834.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1120-1000G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39300801 | |||||||
| chr2:39300994 | T | C | 9 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(6): Show |
9 | HG01433.hp2 NA18942.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1120-1193A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39300994 | |||||||
| chr2:39301067 | GAT | G | 2 | a0001c0002t0001g0077 a0001c0002t0001g0093 |
2 | NA18946.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1120-1268_1120-126 others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39301067 | |||||||
| chr2:39301072 | T | A | 2 | a0001c0002t0001g0077 a0001c0002t0001g0093 |
2 | NA18946.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1120-1271A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39301072 | |||||||
| chr2:39301085 | ACATTT | A | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1120-1289_1120-128 others(9): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39301085 | |||||||
| chr2:39301132 | C | CA | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1120-1332dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39301132 | |||||||
| chr2:39301211 | A | C | 49 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(46): Show |
49 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.1120-1410T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39301211 | |||||||
| chr2:39301254 | A | G | 4 | a0001c0001t0003g0173 a0001c0001t0003g0181 a0001c0001t0003g0186 others(1): Show |
4 | HG02055.hp2 HG02976.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120-1453T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39301254 | |||||||
| chr2:39301699 | T | A | 170 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(167): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1120-1898A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39301699 | |||||||
| chr2:39301711 | G | A | 1 | a0001c0001t0002g0025 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1120-1910C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39301711 | |||||||
| chr2:39301713 | G | A | 1 | a0001c0003t0002g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1120-1912C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39301713 | |||||||
| chr2:39301786 | G | C | 91 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1120-1985C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39301786 | |||||||
| chr2:39301799 | C | T | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1120-1998G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39301799 | |||||||
| chr2:39301978 | T | C | 202 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(199): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1120-2177A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39301978 | |||||||
| chr2:39302046 | A | T | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1120-2245T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39302046 | |||||||
| chr2:39302062 | A | G | 1 | a0001c0001t0003g0174 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1120-2261T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39302062 | |||||||
| chr2:39302271 | T | C | 9 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(6): Show |
9 | HG01433.hp2 NA18942.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1120-2470A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39302271 | |||||||
| chr2:39302407 | A | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1120-2606T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39302407 | |||||||
| chr2:39302487 | G | T | 88 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(85): Show |
88 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1120-2686C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39302487 | |||||||
| chr2:39302735 | A | G | 180 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(177): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1120-2934T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39302735 | |||||||
| chr2:39302839 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1120-3038G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39302839 | |||||||
| chr2:39302886 | C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1120-3085G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39302886 | |||||||
| chr2:39302995 | C | T | 89 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(86): Show |
89 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1120-3194G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39302995 | |||||||
| chr2:39303111 | C | G | 1 | a0001c0001t0003g0206 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1120-3310G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39303111 | |||||||
| chr2:39303331 | G | C | 17 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(14): Show |
17 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1120-3530C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39303331 | |||||||
| chr2:39303467 | A | G | 22 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1120-3666T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39303467 | |||||||
| chr2:39303591 | T | G | 1 | a0001c0002t0001g0095 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1120-3790A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39303591 | |||||||
| chr2:39303817 | G | A | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1120-4016C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39303817 | |||||||
| chr2:39303923 | T | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1119+4020A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39303923 | |||||||
| chr2:39303925 | G | GA | 28 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(25): Show |
28 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1119+4017dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39303925 | |||||||
| chr2:39303933 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1119+4010A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39303933 | |||||||
| chr2:39303974 | T | G | 3 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 |
3 | HG01109.hp2 HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1119+3969A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39303974 | |||||||
| chr2:39303994 | T | C | 1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1119+3949A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39303994 | |||||||
| chr2:39304148 | A | AT | 27 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(24): Show |
27 | HG00140.hp1 HG00408.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.1119+3794dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39304148 | |||||||
| chr2:39304148 | AT | A | 91 | a0001c0001t0003g0185 a0001c0001t0005g0011 a0001c0002t0001g0026 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1119+3794delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39304148 | |||||||
| chr2:39304167 | G | C | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1119+3776C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39304167 | |||||||
| chr2:39304269 | C | T | 1 | a0001c0002t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1119+3674G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39304269 | |||||||
| chr2:39304270 | A | G | 218 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(215): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1119+3673T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39304270 | |||||||
| chr2:39304286 | T | C | 1 | a0001c0003t0004g0232 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1119+3657A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39304286 | |||||||
| chr2:39304614 | G | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1119+3329C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39304614 | |||||||
| chr2:39304940 | A | T | 90 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1119+3003T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39304940 | |||||||
| chr2:39305006 | G | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1119+2937C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305006 | |||||||
| chr2:39305037 | G | A | 28 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(25): Show |
28 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1119+2906C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305037 | |||||||
| chr2:39305053 | G | C | 1 | a0001c0001t0003g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1119+2890C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305053 | |||||||
| chr2:39305133 | G | C | 90 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1119+2810C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305133 | |||||||
| chr2:39305147 | G | A | 4 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0004t0005g0002 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+2796C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305147 | |||||||
| chr2:39305201 | A | G | 208 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(205): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1119+2742T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305201 | |||||||
| chr2:39305285 | A | T | 9 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(6): Show |
9 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1119+2658T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305285 | |||||||
| chr2:39305303 | T | C | 2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1119+2640A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305303 | |||||||
| chr2:39305378 | A | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1119+2565T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305378 | |||||||
| chr2:39305509 | G | C | 90 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1119+2434C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305509 | |||||||
| chr2:39305606 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1119+2337A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305606 | |||||||
| chr2:39305628 | C | T | 3 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 |
3 | HG01496.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1119+2315G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305628 | |||||||
| chr2:39305697 | C | T | 1 | a0001c0003t0002g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1119+2246G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305697 | |||||||
| chr2:39305809 | G | A | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1119+2134C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305809 | |||||||
| chr2:39305830 | AT | A | 28 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0052 others(25): Show |
28 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1119+2112delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305830 | |||||||
| chr2:39305847 | T | A | 1 | a0001c0002t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1119+2096A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305847 | |||||||
| chr2:39305915 | C | T | 8 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(5): Show |
8 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1119+2028G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305915 | |||||||
| chr2:39305997 | T | A | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1119+1946A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39305997 | |||||||
| chr2:39306097 | G | T | 3 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 |
3 | HG00280.hp1 HG00738.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1119+1846C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39306097 | |||||||
| chr2:39306143 | T | A | 9 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(6): Show |
9 | HG01433.hp2 NA18942.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1119+1800A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39306143 | |||||||
| chr2:39306310 | C | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1119+1633G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39306310 | |||||||
| chr2:39306325 | T | C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1119+1618A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39306325 | |||||||
| chr2:39306620 | A | T | 1 | a0001c0002t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1119+1323T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39306620 | |||||||
| chr2:39306626 | C | CT | 4 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0171 others(1): Show |
4 | HG00738.hp2 HG02451.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119+1316dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39306626 | |||||||
| chr2:39307002 | G | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1119+941C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39307002 | |||||||
| chr2:39307532 | T | C | 1 | a0001c0001t0005g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1119+411A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39307532 | |||||||
| chr2:39307565 | CAT | C | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1119+376_1119+377d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39307565 | |||||||
| chr2:39307722 | A | T | 1 | a0001c0001t0005g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1119+221T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39307722 | |||||||
| chr2:39307763 | G | C | 1 | a0001c0002t0001g0125 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1119+180C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39307763 | |||||||
| chr2:39307933 | T | C | 1 | a0001c0001t0002g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1119+10A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 15/33 | chr2 | 39307933 | |||||||
| chr2:39308076 | A | G | 1 | a0001c0001t0002g0054 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1057-71T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 14/33 | chr2 | 39308076 | |||||||
| chr2:39308351 | T | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1057-346A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 14/33 | chr2 | 39308351 | |||||||
| chr2:39308475 | G | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1057-470C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 14/33 | chr2 | 39308475 | |||||||
| chr2:39308702 | T | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1057-697A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 14/33 | chr2 | 39308702 | |||||||
| chr2:39308722 | T | C | 1 | a0001c0002t0001g0112 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1057-717A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 14/33 | chr2 | 39308722 | |||||||
| chr2:39309109 | C | T | 9 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(6): Show |
9 | HG01433.hp2 NA18942.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1056+352G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 14/33 | chr2 | 39309109 | |||||||
| chr2:39309115 | T | TA | 19 | a0001c0002t0001g0026 a0001c0002t0001g0040 a0001c0002t0001g0062 others(16): Show |
19 | HG01106.hp1 HG01928.hp1 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.1056+345dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 14/33 | chr2 | 39309115 | |||||||
| chr2:39309281 | G | A | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1056+180C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 14/33 | chr2 | 39309281 | |||||||
| chr2:39309315 | G | C | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1056+146C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 14/33 | chr2 | 39309315 | |||||||
| chr2:39309548 | A | AT | 22 | a0001c0001t0001g0180 a0001c0001t0003g0186 a0001c0001t0003g0190 others(19): Show |
22 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.998-30dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39309548 | |||||||
| chr2:39309548 | A | ATT | 67 | a0001c0002t0001g0037 a0001c0002t0001g0039 a0001c0002t0001g0040 others(64): Show |
67 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.998-31_998-30dupAA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39309548 | |||||||
| chr2:39309548 | A | ATTT | 24 | a0001c0001t0003g0194 a0001c0001t0006g0205 a0001c0002t0001g0026 others(21): Show |
24 | HG00741.hp2 HG01099.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.998-32_998-30dupAA others(1): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39309548 | |||||||
| chr2:39309548 | AT | A | 61 | a0001c0001t0002g0018 a0001c0001t0002g0020 a0001c0001t0002g0021 others(58): Show |
61 | HG00280.hp1 HG00738.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.998-30delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39309548 | |||||||
| chr2:39309548 | ATT | A | 8 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0055 others(5): Show |
8 | HG00609.hp1 NA18995.hp1 NA18998.hp2 others(5): Show |
intron_variant | MODIFIER | c.998-31_998-30delAA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39309548 | |||||||
| chr2:39309657 | C | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.998-138G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39309657 | |||||||
| chr2:39309845 | A | G | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.998-326T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39309845 | |||||||
| chr2:39309913 | T | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.998-394A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39309913 | |||||||
| chr2:39310079 | T | C | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.998-560A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39310079 | |||||||
| chr2:39310302 | A | G | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.998-783T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39310302 | |||||||
| chr2:39310456 | G | C | 24 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(21): Show |
24 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.998-937C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39310456 | |||||||
| chr2:39310467 | C | G | 135 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.998-948G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39310467 | |||||||
| chr2:39310468 | T | G | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.998-949A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39310468 | |||||||
| chr2:39310577 | T | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.998-1058A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39310577 | |||||||
| chr2:39310582 | G | A | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.998-1063C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39310582 | |||||||
| chr2:39310610 | G | T | 1 | a0001c0002t0001g0058 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.998-1091C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39310610 | |||||||
| chr2:39310773 | G | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.998-1254C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39310773 | |||||||
| chr2:39310838 | A | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.998-1319T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39310838 | |||||||
| chr2:39310861 | T | C | 1 | a0001c0004t0005g0002 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.998-1342A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39310861 | |||||||
| chr2:39310928 | C | T | 1 | a0001c0002t0001g0070 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.998-1409G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39310928 | |||||||
| chr2:39310943 | C | T | 3 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 |
3 | HG01109.hp2 HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.998-1424G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39310943 | |||||||
| chr2:39311024 | T | C | 1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.998-1505A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39311024 | |||||||
| chr2:39311091 | T | C | 2 | a0001c0003t0004g0225 a0001c0003t0004g0226 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.998-1572A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39311091 | |||||||
| chr2:39311138 | C | T | 1 | a0001c0001t0003g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.998-1619G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39311138 | |||||||
| chr2:39311268 | G | T | 1 | a0001c0001t0003g0174 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.998-1749C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39311268 | |||||||
| chr2:39311566 | G | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.998-2047C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39311566 | |||||||
| chr2:39311642 | A | G | 10 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.998-2123T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39311642 | |||||||
| chr2:39311785 | A | G | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.998-2266T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39311785 | |||||||
| chr2:39311848 | T | C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.998-2329A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39311848 | |||||||
| chr2:39311895 | A | G | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.998-2376T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39311895 | |||||||
| chr2:39311962 | G | A | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.998-2443C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39311962 | |||||||
| chr2:39311985 | CA | C | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.998-2467delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39311985 | |||||||
| chr2:39312184 | G | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.998-2665C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39312184 | |||||||
| chr2:39312286 | G | A | 23 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(20): Show |
23 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.998-2767C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39312286 | |||||||
| chr2:39312685 | G | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.997+2625C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39312685 | |||||||
| chr2:39312688 | A | G | 1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.997+2622T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39312688 | |||||||
| chr2:39312792 | G | T | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.997+2518C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39312792 | |||||||
| chr2:39312959 | G | A | 1 | a0001c0004t0005g0002 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.997+2351C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39312959 | |||||||
| chr2:39313016 | T | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.997+2294A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39313016 | |||||||
| chr2:39313131 | C | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.997+2179G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39313131 | |||||||
| chr2:39313258 | G | A | 88 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(85): Show |
88 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.997+2052C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39313258 | |||||||
| chr2:39313397 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.997+1913T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39313397 | |||||||
| chr2:39313442 | TCTTCTTT others(5): Show |
T | 1 | a0001c0001t0002g0020 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.997+1856_997+1867d others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39313442 | |||||||
| chr2:39313455 | CTTCT | C | 87 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(84): Show |
87 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.997+1851_997+1854d others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39313455 | |||||||
| chr2:39313635 | C | G | 1 | a0001c0003t0004g0227 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.997+1675G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39313635 | |||||||
| chr2:39313648 | G | A | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.997+1662C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39313648 | |||||||
| chr2:39313849 | T | C | 1 | a0001c0002t0001g0064 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.997+1461A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39313849 | |||||||
| chr2:39313873 | G | C | 63 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(60): Show |
63 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.997+1437C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39313873 | |||||||
| chr2:39313928 | T | C | 1 | a0001c0001t0002g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.997+1382A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39313928 | |||||||
| chr2:39314114 | C | T | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.997+1196G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39314114 | |||||||
| chr2:39314271 | C | T | 2 | a0001c0002t0001g0069 a0001c0002t0001g0094 |
2 | NA18954.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.997+1039G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39314271 | |||||||
| chr2:39314289 | C | T | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.997+1021G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39314289 | |||||||
| chr2:39314370 | T | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.997+940A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39314370 | |||||||
| chr2:39314391 | T | G | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.997+919A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39314391 | |||||||
| chr2:39314720 | T | C | 22 | a0001c0001t0001g0180 a0001c0001t0002g0152 a0001c0001t0003g0173 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.997+590A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39314720 | |||||||
| chr2:39314853 | T | C | 1 | a0001c0002t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.997+457A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39314853 | |||||||
| chr2:39315209 | A | G | 4 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(1): Show |
4 | HG01496.hp1 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.997+101T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39315209 | |||||||
| chr2:39315224 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.997+86C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 13/33 | chr2 | 39315224 | |||||||
| chr2:39315487 | T | A | 1 | a0001c0001t0005g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.919-99A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39315487 | |||||||
| chr2:39315514 | CA | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.919-127delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39315514 | |||||||
| chr2:39315517 | AT | A | 142 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(139): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.919-130delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39315517 | |||||||
| chr2:39315517 | ATT | A | 21 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(18): Show |
21 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.919-131_919-130del others(2): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39315517 | |||||||
| chr2:39315529 | TA | T | 4 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0002t0001g0112 others(1): Show |
4 | HG03017.hp2 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.919-142delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39315529 | |||||||
| chr2:39315598 | A | C | 23 | a0001c0001t0001g0180 a0001c0001t0002g0152 a0001c0001t0003g0032 others(20): Show |
23 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.919-210T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39315598 | |||||||
| chr2:39315882 | G | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.919-494C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39315882 | |||||||
| chr2:39316272 | T | C | 23 | a0001c0001t0001g0180 a0001c0001t0002g0152 a0001c0001t0003g0032 others(20): Show |
23 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.919-884A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39316272 | |||||||
| chr2:39316315 | A | T | 1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.919-927T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39316315 | |||||||
| chr2:39316338 | A | C | 107 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(104): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.919-950T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39316338 | |||||||
| chr2:39316355 | T | A | 173 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(170): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.919-967A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39316355 | |||||||
| chr2:39316357 | G | A | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.919-969C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39316357 | |||||||
| chr2:39316402 | A | C | 3 | a0001c0002t0001g0089 a0001c0002t0001g0149 a0001c0002t0001g0208 |
3 | HG02738.hp2 HG03239.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.919-1014T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39316402 | |||||||
| chr2:39316525 | A | G | 65 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(62): Show |
65 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.919-1137T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39316525 | |||||||
| chr2:39316745 | C | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.919-1357G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39316745 | |||||||
| chr2:39317131 | C | T | 1 | a0001c0001t0002g0106 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.919-1743G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39317131 | |||||||
| chr2:39317143 | C | G | 33 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(30): Show |
33 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.919-1755G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39317143 | |||||||
| chr2:39317167 | C | T | 1 | a0001c0001t0002g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.919-1779G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39317167 | |||||||
| chr2:39317370 | A | T | 35 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(32): Show |
35 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.919-1982T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39317370 | |||||||
| chr2:39317737 | T | C | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.919-2349A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39317737 | |||||||
| chr2:39317946 | C | A | 1 | a0001c0001t0003g0175 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.919-2558G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39317946 | |||||||
| chr2:39318036 | T | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.919-2648A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318036 | |||||||
| chr2:39318123 | T | A | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.919-2735A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318123 | |||||||
| chr2:39318268 | A | G | 15 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(12): Show |
15 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.919-2880T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318268 | |||||||
| chr2:39318269 | A | G | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-2881T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318269 | |||||||
| chr2:39318412 | G | A | 225 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.919-3024C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318412 | |||||||
| chr2:39318447 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-3059A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318447 | |||||||
| chr2:39318448 | G | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-3060C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318448 | |||||||
| chr2:39318492 | A | G | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.919-3104T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318492 | |||||||
| chr2:39318496 | A | G | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.919-3108T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318496 | |||||||
| chr2:39318588 | A | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-3200T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318588 | |||||||
| chr2:39318662 | T | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-3274A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318662 | |||||||
| chr2:39318663 | A | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-3275T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318663 | |||||||
| chr2:39318688 | G | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-3300C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318688 | |||||||
| chr2:39318847 | A | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-3459T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318847 | |||||||
| chr2:39318848 | G | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-3460C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318848 | |||||||
| chr2:39318864 | A | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-3476T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318864 | |||||||
| chr2:39318869 | T | C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.919-3481A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318869 | |||||||
| chr2:39318874 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.919-3486C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318874 | |||||||
| chr2:39318894 | G | A | 181 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.919-3506C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318894 | |||||||
| chr2:39318936 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.919-3548C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318936 | |||||||
| chr2:39318977 | G | T | 1 | a0001c0001t0014g0189 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.919-3589C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39318977 | |||||||
| chr2:39319008 | A | C | 1 | a0001c0002t0001g0096 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919-3620T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319008 | |||||||
| chr2:39319269 | A | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-3881T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319269 | |||||||
| chr2:39319273 | C | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-3885G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319273 | |||||||
| chr2:39319274 | A | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-3886T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319274 | |||||||
| chr2:39319276 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-3888A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319276 | |||||||
| chr2:39319300 | A | G | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.919-3912T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319300 | |||||||
| chr2:39319314 | G | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-3926C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319314 | |||||||
| chr2:39319335 | T | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-3947A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319335 | |||||||
| chr2:39319346 | C | T | 1 | a0001c0001t0002g0106 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.919-3958G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319346 | |||||||
| chr2:39319350 | C | T | 1 | a0001c0001t0005g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.919-3962G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319350 | |||||||
| chr2:39319351 | A | G | 1 | a0001c0001t0016g0212 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.919-3963T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319351 | |||||||
| chr2:39319400 | G | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4012C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319400 | |||||||
| chr2:39319402 | T | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4014A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319402 | |||||||
| chr2:39319405 | C | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4017G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319405 | |||||||
| chr2:39319408 | G | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4020C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319408 | |||||||
| chr2:39319410 | G | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4022C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319410 | |||||||
| chr2:39319411 | G | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4023C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319411 | |||||||
| chr2:39319413 | T | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4025A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319413 | |||||||
| chr2:39319416 | A | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4028T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319416 | |||||||
| chr2:39319417 | A | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4029T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319417 | |||||||
| chr2:39319418 | A | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4030T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319418 | |||||||
| chr2:39319419 | A | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4031T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319419 | |||||||
| chr2:39319425 | G | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4037C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319425 | |||||||
| chr2:39319426 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4038A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319426 | |||||||
| chr2:39319428 | T | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4040A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319428 | |||||||
| chr2:39319429 | A | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4041T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319429 | |||||||
| chr2:39319430 | C | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4042G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319430 | |||||||
| chr2:39319431 | G | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4043C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319431 | |||||||
| chr2:39319432 | G | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4044C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319432 | |||||||
| chr2:39319433 | A | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4045T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319433 | |||||||
| chr2:39319434 | G | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4046C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319434 | |||||||
| chr2:39319435 | G | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4047C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319435 | |||||||
| chr2:39319436 | A | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4048T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319436 | |||||||
| chr2:39319440 | A | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4052T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319440 | |||||||
| chr2:39319444 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4056A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319444 | |||||||
| chr2:39319445 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4057A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319445 | |||||||
| chr2:39319492 | C | T | 2 | a0001c0002t0001g0039 a0001c0002t0001g0085 |
2 | NA18981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.919-4104G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319492 | |||||||
| chr2:39319493 | G | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4105C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319493 | |||||||
| chr2:39319519 | G | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4131C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319519 | |||||||
| chr2:39319527 | C | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4139G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319527 | |||||||
| chr2:39319527 | C | G | 1 | a0001c0001t0003g0190 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.919-4139G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319527 | |||||||
| chr2:39319554 | A | G | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.919-4166T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319554 | |||||||
| chr2:39319728 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.919-4340C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319728 | |||||||
| chr2:39319746 | G | A | 25 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(22): Show |
25 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.919-4358C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319746 | |||||||
| chr2:39319792 | C | A | 19 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(16): Show |
19 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.919-4404G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319792 | |||||||
| chr2:39319861 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4473A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319861 | |||||||
| chr2:39319891 | A | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4503T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319891 | |||||||
| chr2:39319992 | G | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4604C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319992 | |||||||
| chr2:39319995 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4607A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319995 | |||||||
| chr2:39319997 | T | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4609A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319997 | |||||||
| chr2:39319999 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4611A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39319999 | |||||||
| chr2:39320000 | G | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4612C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320000 | |||||||
| chr2:39320001 | G | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4613C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320001 | |||||||
| chr2:39320006 | T | G | 16 | a0001c0001t0001g0180 a0001c0001t0002g0152 a0001c0001t0003g0032 others(13): Show |
16 | HG01099.hp2 HG01243.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.919-4618A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320006 | |||||||
| chr2:39320010 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4622A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320010 | |||||||
| chr2:39320017 | A | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4629T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320017 | |||||||
| chr2:39320112 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4724A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320112 | |||||||
| chr2:39320116 | A | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4728T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320116 | |||||||
| chr2:39320169 | AGTTAAAT others(36): Show |
A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4824_919-4782d others(45): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320169 | |||||||
| chr2:39320214 | C | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4826G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320214 | |||||||
| chr2:39320222 | G | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4834C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320222 | |||||||
| chr2:39320230 | G | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4842C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320230 | |||||||
| chr2:39320231 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4843A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320231 | |||||||
| chr2:39320233 | G | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4845C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320233 | |||||||
| chr2:39320282 | G | GACTCATA others(4): Show |
1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.919-4895_919-4894i others(13): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320282 | |||||||
| chr2:39320396 | G | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.919-5008C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320396 | |||||||
| chr2:39320434 | G | A | 18 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0089 others(15): Show |
18 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.919-5046C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320434 | |||||||
| chr2:39320505 | AT | A | 9 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(6): Show |
9 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.918+5012delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320505 | |||||||
| chr2:39320656 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.918+4862A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320656 | |||||||
| chr2:39320744 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4774A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320744 | |||||||
| chr2:39320809 | C | T | 1 | a0001c0002t0009g0129 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.918+4709G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320809 | |||||||
| chr2:39320895 | C | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4623G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320895 | |||||||
| chr2:39320903 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4615A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320903 | |||||||
| chr2:39320929 | A | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4589T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320929 | |||||||
| chr2:39320931 | G | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4587C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320931 | |||||||
| chr2:39320932 | A | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4586T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320932 | |||||||
| chr2:39320946 | C | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4572G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320946 | |||||||
| chr2:39320952 | G | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4566C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320952 | |||||||
| chr2:39320954 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.918+4564C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320954 | |||||||
| chr2:39320954 | G | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4564C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320954 | |||||||
| chr2:39320955 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4563A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320955 | |||||||
| chr2:39320957 | G | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4561C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320957 | |||||||
| chr2:39320958 | G | C | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4560C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320958 | |||||||
| chr2:39320959 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4559A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320959 | |||||||
| chr2:39320962 | A | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4556T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320962 | |||||||
| chr2:39320963 | T | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4555A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320963 | |||||||
| chr2:39320968 | G | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4550C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320968 | |||||||
| chr2:39320971 | A | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4547T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320971 | |||||||
| chr2:39320972 | A | G | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4546T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320972 | |||||||
| chr2:39320985 | T | G | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4533A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39320985 | |||||||
| chr2:39321044 | A | G | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.918+4474T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39321044 | |||||||
| chr2:39321132 | G | A | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.918+4386C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39321132 | |||||||
| chr2:39321180 | C | G | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.918+4338G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39321180 | |||||||
| chr2:39321237 | T | C | 116 | a0001c0001t0002g0021 a0001c0001t0003g0173 a0001c0001t0003g0179 others(113): Show |
116 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.918+4281A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39321237 | |||||||
| chr2:39321365 | T | C | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.918+4153A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39321365 | |||||||
| chr2:39321494 | T | C | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.918+4024A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39321494 | |||||||
| chr2:39321500 | A | G | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.918+4018T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39321500 | |||||||
| chr2:39321518 | T | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.918+4000A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39321518 | |||||||
| chr2:39321547 | G | A | 225 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.918+3971C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39321547 | |||||||
| chr2:39321565 | C | G | 2 | a0001c0002t0001g0039 a0001c0002t0001g0085 |
2 | NA18981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.918+3953G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39321565 | |||||||
| chr2:39321570 | C | G | 58 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(55): Show |
58 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.918+3948G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39321570 | |||||||
| chr2:39321607 | A | G | 2 | a0001c0001t0003g0191 a0003c0009t0005g0016 |
2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.918+3911T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39321607 | |||||||
| chr2:39321756 | G | A | 1 | a0001c0002t0001g0125 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.918+3762C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39321756 | |||||||
| chr2:39321874 | G | T | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.918+3644C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39321874 | |||||||
| chr2:39322005 | G | A | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.918+3513C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322005 | |||||||
| chr2:39322246 | A | G | 98 | a0001c0001t0002g0021 a0001c0001t0003g0173 a0001c0001t0003g0179 others(95): Show |
98 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.918+3272T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322246 | |||||||
| chr2:39322442 | C | T | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.918+3076G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322442 | |||||||
| chr2:39322592 | A | ATG | 24 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(21): Show |
24 | HG01243.hp2 HG01496.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.918+2924_918+2925d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322592 | |||||||
| chr2:39322592 | A | ATGTG | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+2922_918+2925d others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322592 | |||||||
| chr2:39322592 | A | ATGTGTG | 13 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0063 others(10): Show |
13 | HG00280.hp2 HG01109.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.918+2920_918+2925d others(8): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322592 | |||||||
| chr2:39322592 | A | ATGTGTGT others(1): Show |
72 | a0001c0001t0003g0173 a0001c0001t0003g0179 a0001c0001t0003g0181 others(69): Show |
72 | HG00408.hp2 HG00609.hp2 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.918+2918_918+2925d others(10): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322592 | |||||||
| chr2:39322592 | A | ATGTGTGT others(3): Show |
10 | a0001c0002t0001g0039 a0001c0002t0001g0085 a0001c0002t0001g0092 others(7): Show |
10 | HG00140.hp2 HG02738.hp2 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.918+2916_918+2925d others(12): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322592 | |||||||
| chr2:39322592 | A | G | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.918+2926T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322592 | |||||||
| chr2:39322592 | ATGTGTG | A | 25 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(22): Show |
25 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.918+2920_918+2925d others(8): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322592 | |||||||
| chr2:39322616 | G | A | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.918+2902C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322616 | |||||||
| chr2:39322616 | GTATA | G | 2 | a0001c0003t0004g0225 a0001c0003t0004g0226 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.918+2898_918+2901d others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322616 | |||||||
| chr2:39322618 | A | G | 132 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(129): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.918+2900T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322618 | |||||||
| chr2:39322620 | A | G | 14 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(11): Show |
14 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.918+2898T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322620 | |||||||
| chr2:39322630 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.918+2888T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322630 | |||||||
| chr2:39322654 | A | T | 12 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(9): Show |
12 | HG01433.hp2 HG03831.hp2 NA18945.hp2 others(9): Show |
intron_variant | MODIFIER | c.918+2864T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322654 | |||||||
| chr2:39322700 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.918+2818G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322700 | |||||||
| chr2:39322812 | C | G | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.918+2706G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322812 | |||||||
| chr2:39322812 | C | T | 6 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(3): Show |
6 | HG03831.hp2 NA18998.hp2 NA19012.hp1 others(3): Show |
intron_variant | MODIFIER | c.918+2706G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322812 | |||||||
| chr2:39322862 | G | A | 1 | a0001c0001t0002g0135 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.918+2656C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322862 | |||||||
| chr2:39322903 | C | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.918+2615G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322903 | |||||||
| chr2:39322914 | C | G | 120 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(117): Show |
120 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.918+2604G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39322914 | |||||||
| chr2:39323088 | G | A | 2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.918+2430C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39323088 | |||||||
| chr2:39323148 | G | A | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.918+2370C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39323148 | |||||||
| chr2:39323338 | A | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.918+2180T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39323338 | |||||||
| chr2:39323467 | C | T | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.918+2051G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39323467 | |||||||
| chr2:39323505 | A | T | 3 | a0001c0003t0004g0215 a0001c0003t0004g0225 a0001c0003t0004g0226 |
3 | HG03490.hp2 HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.918+2013T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39323505 | |||||||
| chr2:39323508 | T | C | 1 | a0001c0002t0001g0038 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.918+2010A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39323508 | |||||||
| chr2:39323517 | T | C | 33 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(30): Show |
33 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.918+2001A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39323517 | |||||||
| chr2:39323528 | A | G | 1 | a0001c0001t0003g0174 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.918+1990T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39323528 | |||||||
| chr2:39323547 | C | G | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.918+1971G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39323547 | |||||||
| chr2:39323586 | T | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.918+1932A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39323586 | |||||||
| chr2:39323654 | A | G | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.918+1864T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39323654 | |||||||
| chr2:39323736 | A | G | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.918+1782T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39323736 | |||||||
| chr2:39323882 | C | T | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.918+1636G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39323882 | |||||||
| chr2:39324008 | A | T | 1 | a0001c0002t0001g0151 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.918+1510T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39324008 | |||||||
| chr2:39324048 | T | C | 2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.918+1470A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39324048 | |||||||
| chr2:39324180 | A | G | 174 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(171): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.918+1338T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39324180 | |||||||
| chr2:39324321 | C | T | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.918+1197G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39324321 | |||||||
| chr2:39324388 | T | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.918+1130A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39324388 | |||||||
| chr2:39324390 | G | C | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.918+1128C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39324390 | |||||||
| chr2:39324446 | T | C | 6 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(3): Show |
6 | HG01496.hp1 HG02717.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.918+1072A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39324446 | |||||||
| chr2:39324477 | C | T | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.918+1041G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39324477 | |||||||
| chr2:39324520 | A | G | 1 | a0001c0002t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.918+998T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39324520 | |||||||
| chr2:39324561 | G | T | 1 | a0001c0003t0004g0219 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.918+957C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39324561 | |||||||
| chr2:39324697 | C | G | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.918+821G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39324697 | |||||||
| chr2:39324800 | T | C | 1 | a0001c0002t0001g0081 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.918+718A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39324800 | |||||||
| chr2:39325070 | G | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.918+448C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39325070 | |||||||
| chr2:39325158 | T | G | 7 | a0001c0002t0001g0062 a0001c0002t0001g0065 a0001c0002t0001g0066 others(4): Show |
7 | NA18948.hp1 NA18952.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+360A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39325158 | |||||||
| chr2:39325232 | A | G | 174 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(171): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.918+286T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39325232 | |||||||
| chr2:39325444 | A | G | 10 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.918+74T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 12/33 | chr2 | 39325444 | |||||||
| chr2:39325696 | A | AAT | 10 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.807+32_807+33dupAT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 11/33 | chr2 | 39325696 | |||||||
| chr2:39325711 | T | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.807+19A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 11/33 | chr2 | 39325711 | |||||||
| chr2:39325986 | C | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.663-25G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 9/33 | chr2 | 39325986 | |||||||
| chr2:39326113 | A | T | 4 | a0001c0002t0001g0095 a0001c0002t0001g0096 a0001c0002t0001g0113 others(1): Show |
4 | HG00280.hp2 HG01109.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.662+33T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 9/33 | chr2 | 39326113 | |||||||
| chr2:39326130 | A | G | 140 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.662+16T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 9/33 | chr2 | 39326130 | |||||||
| chr2:39326350 | A | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.531-73T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39326350 | |||||||
| chr2:39326460 | C | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.531-183G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39326460 | |||||||
| chr2:39326586 | G | T | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.531-309C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39326586 | |||||||
| chr2:39326605 | C | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.531-328G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39326605 | |||||||
| chr2:39326639 | G | C | 3 | a0001c0002t0001g0062 a0001c0002t0001g0065 a0002c0010t0005g0017 |
3 | HG02615.hp1 NA18982.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.531-362C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39326639 | |||||||
| chr2:39326735 | G | C | 3 | a0001c0002t0001g0084 a0001c0002t0001g0127 a0001c0002t0001g0133 |
3 | HG01975.hp1 HG01978.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.531-458C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39326735 | |||||||
| chr2:39326844 | C | T | 6 | a0001c0003t0004g0214 a0001c0003t0004g0217 a0001c0003t0004g0218 others(3): Show |
6 | HG00408.hp1 NA18954.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.531-567G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39326844 | |||||||
| chr2:39326888 | C | G | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.531-611G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39326888 | |||||||
| chr2:39326908 | T | G | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.531-631A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39326908 | |||||||
| chr2:39326913 | C | A | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.531-636G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39326913 | |||||||
| chr2:39327076 | C | T | 4 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0004t0005g0002 others(1): Show |
4 | HG02895.hp1 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.531-799G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39327076 | |||||||
| chr2:39327157 | C | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.531-880G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39327157 | |||||||
| chr2:39327235 | A | G | 98 | a0001c0001t0003g0173 a0001c0001t0003g0179 a0001c0001t0003g0181 others(95): Show |
98 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.531-958T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39327235 | |||||||
| chr2:39327277 | A | G | 20 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0003t0004g0214 others(17): Show |
20 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.531-1000T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39327277 | |||||||
| chr2:39327311 | G | T | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.531-1034C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39327311 | |||||||
| chr2:39327460 | C | T | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.531-1183G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39327460 | |||||||
| chr2:39327703 | AAAATTTA others(177): Show |
A | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.531-1610_531-1427d others(2): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39327703 | |||||||
| chr2:39327728 | C | T | 23 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(20): Show |
23 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.531-1451G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39327728 | |||||||
| chr2:39328079 | C | T | 1 | a0001c0002t0001g0074 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.531-1802G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39328079 | |||||||
| chr2:39328106 | G | A | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.531-1829C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39328106 | |||||||
| chr2:39328200 | G | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.531-1923C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39328200 | |||||||
| chr2:39328290 | G | A | 1 | a0001c0001t0014g0189 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.531-2013C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39328290 | |||||||
| chr2:39328530 | G | A | 2 | a0001c0002t0001g0046 a0001c0002t0001g0047 |
2 | HG01358.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.531-2253C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39328530 | |||||||
| chr2:39328540 | CA | C | 7 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.531-2264delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39328540 | |||||||
| chr2:39328758 | A | T | 112 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(109): Show |
112 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.531-2481T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39328758 | |||||||
| chr2:39328799 | G | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.531-2522C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39328799 | |||||||
| chr2:39328803 | G | A | 90 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.531-2526C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39328803 | |||||||
| chr2:39328875 | A | G | 1 | a0001c0001t0003g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.531-2598T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39328875 | |||||||
| chr2:39328963 | G | A | 2 | a0001c0001t0002g0116 a0001c0001t0002g0136 |
2 | NA18948.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.531-2686C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39328963 | |||||||
| chr2:39328996 | G | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.531-2719C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39328996 | |||||||
| chr2:39329070 | A | C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.531-2793T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39329070 | |||||||
| chr2:39329112 | T | C | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.530+2805A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39329112 | |||||||
| chr2:39329117 | C | G | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.530+2800G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39329117 | |||||||
| chr2:39329160 | G | A | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.530+2757C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39329160 | |||||||
| chr2:39329200 | A | G | 1 | a0001c0001t0003g0174 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.530+2717T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39329200 | |||||||
| chr2:39329212 | G | T | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.530+2705C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39329212 | |||||||
| chr2:39329430 | A | C | 9 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(6): Show |
9 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+2487T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39329430 | |||||||
| chr2:39329643 | C | T | 90 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.530+2274G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39329643 | |||||||
| chr2:39329659 | G | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.530+2258C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39329659 | |||||||
| chr2:39329722 | A | T | 18 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(15): Show |
18 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.530+2195T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39329722 | |||||||
| chr2:39330057 | G | A | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.530+1860C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39330057 | |||||||
| chr2:39330261 | G | A | 22 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(19): Show |
22 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.530+1656C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39330261 | |||||||
| chr2:39330307 | T | C | 22 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.530+1610A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39330307 | |||||||
| chr2:39330591 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.530+1326G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39330591 | |||||||
| chr2:39330649 | A | T | 20 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0003t0004g0214 others(17): Show |
20 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.530+1268T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39330649 | |||||||
| chr2:39330673 | G | T | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.530+1244C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39330673 | |||||||
| chr2:39330871 | A | G | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0130 |
3 | NA18948.hp1 NA18960.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.530+1046T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39330871 | |||||||
| chr2:39330923 | G | A | 2 | a0001c0001t0003g0182 a0001c0001t0003g0185 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.530+994C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39330923 | |||||||
| chr2:39330947 | T | C | 1 | a0001c0002t0001g0037 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.530+970A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39330947 | |||||||
| chr2:39331060 | T | C | 8 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(5): Show |
8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.530+857A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39331060 | |||||||
| chr2:39331100 | G | A | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.530+817C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39331100 | |||||||
| chr2:39331165 | A | G | 22 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0015g0192 others(19): Show |
22 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.530+752T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39331165 | |||||||
| chr2:39331233 | A | G | 172 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(169): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.530+684T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39331233 | |||||||
| chr2:39331446 | G | A | 18 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(15): Show |
18 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.530+471C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39331446 | |||||||
| chr2:39331511 | G | A | 3 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0055 |
3 | NA18998.hp2 NA19012.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.530+406C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39331511 | |||||||
| chr2:39331787 | G | A | 170 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(167): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.530+130C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 8/33 | chr2 | 39331787 | |||||||
| chr2:39332120 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.458-131A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 7/33 | chr2 | 39332120 | |||||||
| chr2:39332144 | T | C | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-155A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 7/33 | chr2 | 39332144 | |||||||
| chr2:39332358 | T | G | 23 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(20): Show |
23 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.458-369A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 7/33 | chr2 | 39332358 | |||||||
| chr2:39332617 | T | C | 2 | a0001c0001t0002g0107 a0001c0001t0002g0135 |
2 | HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.458-628A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 7/33 | chr2 | 39332617 | |||||||
| chr2:39332703 | T | C | 22 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.458-714A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 7/33 | chr2 | 39332703 | |||||||
| chr2:39332918 | C | G | 23 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(20): Show |
23 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.457+614G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 7/33 | chr2 | 39332918 | |||||||
| chr2:39333059 | A | G | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.457+473T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 7/33 | chr2 | 39333059 | |||||||
| chr2:39333097 | G | A | 2 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
2 | HG01106.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.457+435C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 7/33 | chr2 | 39333097 | |||||||
| chr2:39333123 | C | T | 5 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(2): Show |
5 | HG03831.hp2 NA18998.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.457+409G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 7/33 | chr2 | 39333123 | |||||||
| chr2:39333154 | A | C | 1 | a0001c0004t0013g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.457+378T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 7/33 | chr2 | 39333154 | |||||||
| chr2:39333215 | T | C | 24 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(21): Show |
24 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.457+317A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 7/33 | chr2 | 39333215 | |||||||
| chr2:39333453 | T | A | 2 | a0001c0002t0001g0039 a0001c0002t0001g0085 |
2 | NA18981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.457+79A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 7/33 | chr2 | 39333453 | |||||||
| chr2:39333469 | AAC | A | 18 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(15): Show |
18 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.457+61_457+62delGT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 7/33 | chr2 | 39333469 | |||||||
| chr2:39333507 | C | T | 1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.457+25G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 7/33 | chr2 | 39333507 | |||||||
| chr2:39333829 | A | G | 104 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.415-255T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39333829 | |||||||
| chr2:39333959 | T | TTGTG | 8 | a0001c0002t0001g0040 a0001c0002t0001g0062 a0001c0002t0001g0064 others(5): Show |
8 | HG01928.hp1 HG01978.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-386_415-385ins others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39333959 | |||||||
| chr2:39333959 | T | TTGTGTG | 3 | a0001c0002t0001g0081 a0001c0002t0001g0124 a0001c0002t0001g0193 |
3 | HG01952.hp2 NA18948.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.415-386_415-385ins others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39333959 | |||||||
| chr2:39333961 | T | G | 14 | a0001c0002t0001g0040 a0001c0002t0001g0062 a0001c0002t0001g0064 others(11): Show |
14 | HG01106.hp1 HG01928.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.415-387A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39333961 | |||||||
| chr2:39333961 | T | TTG | 42 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(39): Show |
42 | HG00609.hp1 HG00741.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.415-389_415-388dup others(2): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39333961 | |||||||
| chr2:39333961 | T | TTGTG | 56 | a0001c0001t0002g0099 a0001c0001t0002g0135 a0001c0001t0002g0137 others(53): Show |
56 | HG00280.hp2 HG00408.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.415-391_415-388dup others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39333961 | |||||||
| chr2:39333961 | T | TTGTGTG | 10 | a0001c0001t0002g0119 a0001c0002t0001g0070 a0001c0002t0001g0111 others(7): Show |
10 | HG01099.hp1 HG02165.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.415-393_415-388dup others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39333961 | |||||||
| chr2:39333961 | TTG | T | 24 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0052 others(21): Show |
24 | HG00280.hp1 HG00738.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.415-389_415-388del others(2): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39333961 | |||||||
| chr2:39333961 | TTGTG | T | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0035 others(3): Show |
6 | HG02257.hp1 HG02486.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-391_415-388del others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39333961 | |||||||
| chr2:39333961 | TTGTGTG | T | 9 | a0001c0001t0005g0015 a0001c0001t0006g0198 a0001c0001t0006g0199 others(6): Show |
9 | HG01433.hp2 HG03579.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.415-393_415-388del others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39333961 | |||||||
| chr2:39333961 | TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0002g0141 a0001c0001t0003g0190 a0001c0003t0005g0005 |
3 | HG02109.hp1 HG03579.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.415-395_415-388del others(8): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39333961 | |||||||
| chr2:39333961 | TTGTGTGT others(5): Show |
T | 39 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(36): Show |
39 | HG00140.hp1 HG00408.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.415-399_415-388del others(12): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39333961 | |||||||
| chr2:39333961 | TTGTGTGT others(7): Show |
T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.415-401_415-388del others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39333961 | |||||||
| chr2:39333961 | TTGTGTGT others(13): Show |
T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.415-407_415-388del others(20): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39333961 | |||||||
| chr2:39334000 | T | TGTG | 2 | a0001c0002t0001g0089 a0001c0002t0001g0128 |
2 | HG01952.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.415-427_415-426ins others(3): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39334000 | |||||||
| chr2:39334001 | T | G | 1 | a0001c0008t0002g0088 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.415-427A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39334001 | |||||||
| chr2:39334328 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.415-754C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39334328 | |||||||
| chr2:39334446 | GA | G | 88 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(85): Show |
88 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.415-873delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39334446 | |||||||
| chr2:39334647 | T | C | 22 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.415-1073A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39334647 | |||||||
| chr2:39334704 | C | A | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.415-1130G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39334704 | |||||||
| chr2:39334914 | G | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.415-1340C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39334914 | |||||||
| chr2:39335179 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.415-1605A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39335179 | |||||||
| chr2:39335210 | T | C | 1 | a0001c0003t0004g0227 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.415-1636A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39335210 | |||||||
| chr2:39335394 | G | A | 7 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(4): Show |
7 | HG01496.hp1 HG03195.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+1526C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39335394 | |||||||
| chr2:39335710 | T | C | 2 | a0001c0001t0002g0099 a0001c0001t0002g0137 |
2 | HG01496.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.414+1210A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39335710 | |||||||
| chr2:39335773 | A | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.414+1147T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39335773 | |||||||
| chr2:39336210 | G | A | 1 | a0003c0009t0005g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.414+710C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39336210 | |||||||
| chr2:39336252 | C | G | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.414+668G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39336252 | |||||||
| chr2:39336262 | C | G | 1 | a0001c0001t0002g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.414+658G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39336262 | |||||||
| chr2:39336292 | A | G | 52 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(49): Show |
52 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.414+628T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39336292 | |||||||
| chr2:39336347 | G | A | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.414+573C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39336347 | |||||||
| chr2:39336380 | G | C | 1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.414+540C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39336380 | |||||||
| chr2:39336471 | C | CA | 34 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0045 others(31): Show |
34 | HG00140.hp1 HG00609.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.414+448dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39336471 | |||||||
| chr2:39336471 | C | CAA | 21 | a0001c0001t0002g0021 a0001c0001t0002g0023 a0001c0001t0002g0024 others(18): Show |
21 | HG01081.hp2 HG01167.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.414+447_414+448dup others(2): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39336471 | |||||||
| chr2:39336471 | C | CAAA | 11 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0102 others(8): Show |
11 | HG00741.hp1 HG01099.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+446_414+448dup others(3): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39336471 | |||||||
| chr2:39336471 | C | CAAAA | 8 | a0001c0001t0002g0018 a0001c0001t0002g0027 a0001c0001t0002g0029 others(5): Show |
8 | HG01358.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+445_414+448dup others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39336471 | |||||||
| chr2:39336471 | CA | C | 71 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(68): Show |
71 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.414+448delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39336471 | |||||||
| chr2:39336471 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0002g0135 a0001c0001t0015g0192 |
2 | HG02922.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.414+439_414+448del others(10): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39336471 | |||||||
| chr2:39336471 | CAAAAAAA others(4): Show |
C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.414+438_414+448del others(11): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39336471 | |||||||
| chr2:39336495 | A | G | 2 | a0001c0002t0001g0145 a0001c0002t0001g0146 |
2 | HG01168.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.414+425T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39336495 | |||||||
| chr2:39336793 | ATCAC | A | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.414+123_414+126del others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 6/33 | chr2 | 39336793 | |||||||
| chr2:39337068 | A | C | 1 | a0001c0001t0003g0178 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.367-101T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 5/33 | chr2 | 39337068 | |||||||
| chr2:39337153 | A | G | 1 | a0001c0002t0001g0138 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.367-186T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 5/33 | chr2 | 39337153 | |||||||
| chr2:39337181 | A | G | 2 | a0001c0002t0001g0039 a0001c0002t0001g0085 |
2 | NA18981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.367-214T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 5/33 | chr2 | 39337181 | |||||||
| chr2:39337189 | A | G | 1 | a0001c0001t0003g0175 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.367-222T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 5/33 | chr2 | 39337189 | |||||||
| chr2:39337305 | T | A | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.366+221A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 5/33 | chr2 | 39337305 | |||||||
| chr2:39337470 | TAAGTA | T | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.366+51_366+55delTA others(3): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 5/33 | chr2 | 39337470 | |||||||
| chr2:39337479 | C | A | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.366+47G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 5/33 | chr2 | 39337479 | |||||||
| chr2:39337622 | G | A | 1 | a0001c0002t0001g0074 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.311-41C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39337622 | |||||||
| chr2:39337752 | G | GT | 87 | a0001c0001t0002g0020 a0001c0001t0002g0027 a0001c0001t0002g0028 others(84): Show |
87 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.311-172dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39337752 | |||||||
| chr2:39337752 | G | GTT | 35 | a0001c0001t0002g0035 a0001c0001t0003g0032 a0001c0002t0001g0026 others(32): Show |
35 | HG00408.hp2 HG00609.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.311-173_311-172dup others(2): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39337752 | |||||||
| chr2:39337752 | G | GTTT | 9 | a0001c0002t0001g0122 a0001c0002t0001g0125 a0001c0002t0001g0197 others(6): Show |
9 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.311-174_311-172dup others(3): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39337752 | |||||||
| chr2:39337752 | G | GTTTT | 6 | a0001c0003t0004g0215 a0001c0003t0004g0219 a0001c0003t0004g0225 others(3): Show |
6 | HG03490.hp2 HG03492.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-175_311-172dup others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39337752 | |||||||
| chr2:39337752 | G | GTTTTT | 8 | a0001c0001t0002g0052 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
8 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.311-176_311-172dup others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39337752 | |||||||
| chr2:39337752 | G | GTTTTTTT | 6 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0013 others(3): Show |
6 | HG01168.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.311-178_311-172dup others(7): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39337752 | |||||||
| chr2:39337752 | G | GTTTTTTT others(3): Show |
4 | a0001c0001t0006g0200 a0001c0001t0006g0202 a0001c0001t0006g0203 others(1): Show |
4 | HG01884.hp2 NA18981.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.311-181_311-172dup others(10): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39337752 | |||||||
| chr2:39337752 | G | GTTTTTTT others(4): Show |
7 | a0001c0001t0005g0010 a0001c0001t0006g0198 a0001c0001t0006g0199 others(4): Show |
7 | HG01243.hp1 HG01433.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.311-182_311-172dup others(11): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39337752 | |||||||
| chr2:39337752 | G | T | 3 | a0001c0003t0004g0216 a0001c0003t0004g0231 a0001c0003t0004g0232 |
3 | HG02129.hp2 HG02132.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.311-171C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39337752 | |||||||
| chr2:39337898 | C | A | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.311-317G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39337898 | |||||||
| chr2:39337954 | G | A | 1 | a0001c0002t0007g0230 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.311-373C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39337954 | |||||||
| chr2:39338032 | G | C | 2 | a0001c0001t0002g0104 a0001c0001t0002g0108 |
2 | NA18995.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.311-451C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39338032 | |||||||
| chr2:39338431 | T | C | 111 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(108): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.311-850A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39338431 | |||||||
| chr2:39338576 | C | T | 1 | a0001c0001t0002g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.311-995G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39338576 | |||||||
| chr2:39338694 | A | C | 39 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(36): Show |
39 | HG00609.hp1 HG00741.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.311-1113T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39338694 | |||||||
| chr2:39338844 | T | G | 1 | a0001c0002t0001g0207 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.311-1263A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39338844 | |||||||
| chr2:39338917 | G | A | 21 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0046 others(18): Show |
21 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.311-1336C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39338917 | |||||||
| chr2:39339086 | A | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.311-1505T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39339086 | |||||||
| chr2:39339186 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.311-1605T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39339186 | |||||||
| chr2:39339554 | T | C | 1 | a0001c0002t0010g0211 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.311-1973A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39339554 | |||||||
| chr2:39340032 | AT | A | 22 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.311-2452delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39340032 | |||||||
| chr2:39340371 | T | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.311-2790A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39340371 | |||||||
| chr2:39340559 | T | C | 1 | a0001c0002t0010g0211 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.310+2829A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39340559 | |||||||
| chr2:39340752 | A | C | 1 | a0001c0002t0001g0081 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.310+2636T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39340752 | |||||||
| chr2:39340958 | A | G | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.310+2430T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39340958 | |||||||
| chr2:39341014 | C | G | 133 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.310+2374G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39341014 | |||||||
| chr2:39341045 | A | C | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.310+2343T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39341045 | |||||||
| chr2:39341156 | A | G | 1 | a0001c0003t0004g0222 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.310+2232T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39341156 | |||||||
| chr2:39341216 | T | C | 1 | a0001c0001t0006g0198 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.310+2172A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39341216 | |||||||
| chr2:39341296 | C | T | 2 | a0001c0002t0001g0082 a0001c0002t0001g0130 |
2 | NA18960.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.310+2092G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39341296 | |||||||
| chr2:39341459 | C | T | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.310+1929G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39341459 | |||||||
| chr2:39341502 | T | C | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.310+1886A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39341502 | |||||||
| chr2:39341605 | G | A | 1 | a0001c0002t0001g0080 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.310+1783C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39341605 | |||||||
| chr2:39341633 | G | A | 11 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(8): Show |
11 | HG00738.hp2 HG01496.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.310+1755C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39341633 | |||||||
| chr2:39341675 | C | G | 91 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.310+1713G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39341675 | |||||||
| chr2:39341833 | C | T | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.310+1555G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39341833 | |||||||
| chr2:39341899 | T | C | 1 | a0001c0001t0005g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.310+1489A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39341899 | |||||||
| chr2:39342088 | T | G | 2 | a0001c0001t0003g0176 a0001c0001t0003g0177 |
2 | HG01099.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.310+1300A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342088 | |||||||
| chr2:39342106 | T | A | 1 | a0001c0002t0001g0057 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.310+1282A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342106 | |||||||
| chr2:39342108 | G | GTAT | 17 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(14): Show |
17 | HG01081.hp2 HG01167.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.310+1277_310+1279d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342108 | |||||||
| chr2:39342108 | G | GTATTAT | 10 | a0001c0001t0002g0018 a0001c0001t0002g0100 a0001c0001t0002g0101 others(7): Show |
10 | HG00609.hp1 HG01255.hp1 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.310+1274_310+1279d others(8): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342108 | |||||||
| chr2:39342108 | GTAT | G | 20 | a0001c0001t0002g0117 a0001c0001t0002g0119 a0001c0001t0002g0152 others(17): Show |
20 | HG00738.hp2 HG00741.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.310+1277_310+1279d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342108 | |||||||
| chr2:39342108 | GTATTAT | G | 9 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0098 others(6): Show |
9 | HG00408.hp2 HG01257.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.310+1274_310+1279d others(8): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342108 | |||||||
| chr2:39342108 | GTATTATT others(2): Show |
G | 34 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0011 others(31): Show |
34 | HG00280.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.310+1271_310+1279d others(11): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342108 | |||||||
| chr2:39342108 | GTATTATT others(5): Show |
G | 73 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(70): Show |
73 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.310+1268_310+1279d others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342108 | |||||||
| chr2:39342108 | GTATTATT others(8): Show |
G | 41 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(38): Show |
41 | HG00140.hp1 HG00408.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.310+1265_310+1279d others(17): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342108 | |||||||
| chr2:39342108 | GTATTATT others(11): Show |
G | 2 | a0001c0002t0001g0076 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.310+1262_310+1279d others(20): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342108 | |||||||
| chr2:39342108 | GTATTATT others(14): Show |
G | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.310+1259_310+1279d others(23): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342108 | |||||||
| chr2:39342108 | GTATTATT others(17): Show |
G | 1 | a0001c0002t0001g0149 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.310+1256_310+1279d others(26): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342108 | |||||||
| chr2:39342214 | C | G | 23 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(20): Show |
23 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.310+1174G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342214 | |||||||
| chr2:39342414 | G | A | 2 | a0001c0001t0002g0104 a0001c0001t0002g0108 |
2 | NA18995.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.310+974C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342414 | |||||||
| chr2:39342425 | C | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.310+963G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342425 | |||||||
| chr2:39342618 | T | C | 1 | a0001c0002t0001g0138 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.310+770A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342618 | |||||||
| chr2:39342730 | A | G | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.310+658T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39342730 | |||||||
| chr2:39343007 | T | C | 1 | a0001c0002t0001g0047 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.310+381A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39343007 | |||||||
| chr2:39343106 | A | G | 2 | a0001c0003t0004g0225 a0001c0003t0004g0226 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.310+282T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39343106 | |||||||
| chr2:39343260 | T | A | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.310+128A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39343260 | |||||||
| chr2:39343286 | T | C | 111 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(108): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.310+102A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39343286 | |||||||
| chr2:39343328 | A | C | 18 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(15): Show |
18 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.310+60T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 4/33 | chr2 | 39343328 | |||||||
| chr2:39343566 | G | A | 1 | a0001c0003t0004g0217 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.246-114C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39343566 | |||||||
| chr2:39343659 | T | C | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.246-207A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39343659 | |||||||
| chr2:39343774 | C | T | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.246-322G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39343774 | |||||||
| chr2:39344087 | C | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.246-635G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39344087 | |||||||
| chr2:39344160 | C | T | 1 | a0001c0004t0005g0002 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.246-708G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39344160 | |||||||
| chr2:39344164 | T | A | 1 | a0001c0002t0009g0129 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.246-712A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39344164 | |||||||
| chr2:39344212 | T | C | 3 | a0001c0002t0001g0079 a0001c0002t0001g0121 a0001c0002t0001g0122 |
3 | HG02257.hp1 HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.246-760A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39344212 | |||||||
| chr2:39344253 | C | T | 1 | a0001c0002t0001g0070 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.246-801G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39344253 | |||||||
| chr2:39344339 | G | A | 1 | a0001c0002t0001g0196 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.246-887C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39344339 | |||||||
| chr2:39344363 | G | A | 22 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.246-911C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39344363 | |||||||
| chr2:39344490 | C | T | 1 | a0001c0001t0002g0019 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.246-1038G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39344490 | |||||||
| chr2:39344554 | G | A | 2 | a0001c0001t0002g0104 a0001c0001t0002g0108 |
2 | NA18995.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.246-1102C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39344554 | |||||||
| chr2:39344652 | G | T | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.246-1200C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39344652 | |||||||
| chr2:39344781 | C | T | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.246-1329G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39344781 | |||||||
| chr2:39345204 | T | C | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.246-1752A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345204 | |||||||
| chr2:39345273 | G | A | 1 | a0001c0004t0013g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.246-1821C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345273 | |||||||
| chr2:39345291 | A | G | 23 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(20): Show |
23 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.246-1839T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345291 | |||||||
| chr2:39345294 | G | A | 9 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(6): Show |
9 | HG01433.hp2 HG03209.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.246-1842C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345294 | |||||||
| chr2:39345305 | A | G | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.246-1853T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345305 | |||||||
| chr2:39345408 | T | C | 1 | a0001c0001t0002g0045 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.246-1956A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345408 | |||||||
| chr2:39345531 | T | C | 1 | a0001c0002t0001g0084 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.246-2079A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345531 | |||||||
| chr2:39345628 | A | C | 1 | a0001c0002t0001g0081 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.246-2176T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345628 | |||||||
| chr2:39345637 | G | A | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.246-2185C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345637 | |||||||
| chr2:39345652 | G | T | 1 | a0001c0002t0010g0213 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.246-2200C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345652 | |||||||
| chr2:39345708 | A | G | 6 | a0001c0001t0003g0173 a0001c0001t0003g0181 a0001c0001t0003g0186 others(3): Show |
6 | HG02055.hp2 HG02895.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-2256T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345708 | |||||||
| chr2:39345794 | T | C | 170 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(167): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.246-2342A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345794 | |||||||
| chr2:39345865 | T | C | 3 | a0001c0002t0001g0131 a0001c0002t0001g0132 a0001c0002t0001g0151 |
3 | HG03831.hp1 HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.246-2413A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345865 | |||||||
| chr2:39345921 | C | CA | 75 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(72): Show |
75 | HG00738.hp2 HG00741.hp2 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.246-2470dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345921 | |||||||
| chr2:39345921 | C | CAA | 24 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0055 others(21): Show |
24 | HG00280.hp1 HG00609.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.246-2471_246-2470d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345921 | |||||||
| chr2:39345921 | C | CAAAAAAA others(7): Show |
1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.246-2483_246-2470d others(16): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345921 | |||||||
| chr2:39345921 | CA | C | 6 | a0001c0002t0001g0039 a0001c0002t0001g0085 a0001c0002t0010g0211 others(3): Show |
6 | HG01884.hp1 HG02109.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-2470delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345921 | |||||||
| chr2:39345921 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.246-2479_246-2470d others(12): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345921 | |||||||
| chr2:39345991 | A | G | 1 | a0001c0001t0005g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.246-2539T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39345991 | |||||||
| chr2:39346080 | C | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.246-2628G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39346080 | |||||||
| chr2:39346141 | A | G | 144 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.246-2689T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39346141 | |||||||
| chr2:39346380 | C | A | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.246-2928G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39346380 | |||||||
| chr2:39346647 | G | C | 1 | a0001c0002t0001g0127 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.246-3195C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39346647 | |||||||
| chr2:39346673 | G | A | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.246-3221C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39346673 | |||||||
| chr2:39346799 | T | C | 24 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(21): Show |
24 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.246-3347A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39346799 | |||||||
| chr2:39346801 | C | T | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.246-3349G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39346801 | |||||||
| chr2:39346985 | A | C | 23 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(20): Show |
23 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.246-3533T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39346985 | |||||||
| chr2:39347058 | A | G | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.246-3606T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39347058 | |||||||
| chr2:39347150 | C | T | 107 | a0001c0001t0002g0209 a0001c0002t0001g0026 a0001c0002t0001g0037 others(104): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.246-3698G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39347150 | |||||||
| chr2:39347278 | C | T | 3 | a0001c0003t0005g0005 a0001c0003t0005g0006 a0001c0003t0012g0004 |
3 | HG01884.hp1 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.246-3826G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39347278 | |||||||
| chr2:39347387 | T | C | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.246-3935A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39347387 | |||||||
| chr2:39347547 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.246-4095C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39347547 | |||||||
| chr2:39347597 | CTTAAT | C | 18 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(15): Show |
18 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.246-4150_246-4146d others(7): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39347597 | |||||||
| chr2:39347646 | A | G | 1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.246-4194T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39347646 | |||||||
| chr2:39347650 | CTT | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.246-4200_246-4199d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39347650 | |||||||
| chr2:39347782 | G | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.246-4330C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39347782 | |||||||
| chr2:39347821 | T | C | 8 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(5): Show |
8 | HG01496.hp1 HG02717.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.246-4369A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39347821 | |||||||
| chr2:39347843 | A | G | 136 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(133): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.246-4391T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39347843 | |||||||
| chr2:39347876 | G | C | 3 | a0001c0002t0001g0089 a0001c0002t0001g0149 a0001c0002t0001g0208 |
3 | HG02738.hp2 HG03239.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.246-4424C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39347876 | |||||||
| chr2:39347903 | T | C | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.246-4451A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39347903 | |||||||
| chr2:39347949 | G | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.246-4497C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39347949 | |||||||
| chr2:39347962 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.246-4510G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39347962 | |||||||
| chr2:39348195 | T | A | 4 | a0001c0001t0003g0164 a0001c0001t0003g0166 a0001c0001t0003g0169 others(1): Show |
4 | HG02717.hp2 HG03209.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.246-4743A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39348195 | |||||||
| chr2:39348234 | A | T | 107 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(104): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.246-4782T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39348234 | |||||||
| chr2:39348275 | T | C | 1 | a0001c0002t0001g0127 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.246-4823A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39348275 | |||||||
| chr2:39348300 | T | A | 1 | a0001c0001t0002g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.246-4848A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39348300 | |||||||
| chr2:39348336 | T | G | 1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.246-4884A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39348336 | |||||||
| chr2:39348666 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.246-5214T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39348666 | |||||||
| chr2:39348746 | A | C | 1 | a0001c0002t0001g0115 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.246-5294T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39348746 | |||||||
| chr2:39348835 | G | C | 1 | a0001c0001t0002g0123 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.246-5383C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39348835 | |||||||
| chr2:39348864 | C | T | 7 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(4): Show |
7 | HG01496.hp1 HG03195.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.246-5412G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39348864 | |||||||
| chr2:39349100 | G | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.246-5648C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39349100 | |||||||
| chr2:39349102 | A | G | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.246-5650T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39349102 | |||||||
| chr2:39349173 | C | A | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.246-5721G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39349173 | |||||||
| chr2:39349216 | T | C | 1 | a0001c0001t0003g0175 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.246-5764A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39349216 | |||||||
| chr2:39349434 | G | T | 1 | a0001c0002t0001g0067 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.246-5982C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39349434 | |||||||
| chr2:39349589 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.246-6137G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39349589 | |||||||
| chr2:39349613 | C | T | 4 | a0001c0003t0005g0005 a0001c0003t0005g0006 a0001c0003t0011g0001 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.246-6161G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39349613 | |||||||
| chr2:39349655 | G | A | 112 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(109): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.246-6203C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39349655 | |||||||
| chr2:39349734 | G | A | 1 | a0001c0004t0005g0002 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.246-6282C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39349734 | |||||||
| chr2:39349788 | A | C | 3 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0055 |
3 | NA18998.hp2 NA19012.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.246-6336T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39349788 | |||||||
| chr2:39349845 | C | A | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.246-6393G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39349845 | |||||||
| chr2:39349927 | C | T | 1 | a0001c0001t0005g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.245+6322G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39349927 | |||||||
| chr2:39350044 | A | G | 22 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.245+6205T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39350044 | |||||||
| chr2:39350162 | A | G | 22 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.245+6087T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39350162 | |||||||
| chr2:39350661 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.245+5588G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39350661 | |||||||
| chr2:39350680 | T | C | 23 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(20): Show |
23 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.245+5569A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39350680 | |||||||
| chr2:39350684 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.245+5565G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39350684 | |||||||
| chr2:39350759 | C | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.245+5490G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39350759 | |||||||
| chr2:39350844 | C | T | 104 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.245+5405G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39350844 | |||||||
| chr2:39350865 | G | A | 4 | a0001c0002t0001g0128 a0001c0002t0001g0131 a0001c0002t0001g0132 others(1): Show |
4 | HG01952.hp1 HG03831.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+5384C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39350865 | |||||||
| chr2:39350878 | G | A | 21 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0046 others(18): Show |
21 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.245+5371C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39350878 | |||||||
| chr2:39350895 | C | A | 1 | a0001c0002t0001g0063 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.245+5354G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39350895 | |||||||
| chr2:39351244 | T | G | 24 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(21): Show |
24 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.245+5005A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39351244 | |||||||
| chr2:39351251 | T | A | 1 | a0001c0003t0004g0215 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.245+4998A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39351251 | |||||||
| chr2:39351465 | C | G | 1 | a0001c0001t0002g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.245+4784G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39351465 | |||||||
| chr2:39351467 | T | C | 1 | a0001c0002t0001g0040 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.245+4782A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39351467 | |||||||
| chr2:39351493 | G | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.245+4756C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39351493 | |||||||
| chr2:39351528 | T | TCGTA | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.245+4720_245+4721i others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39351528 | |||||||
| chr2:39351598 | T | C | 1 | a0001c0001t0002g0141 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.245+4651A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39351598 | |||||||
| chr2:39351723 | T | C | 163 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(160): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.245+4526A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39351723 | |||||||
| chr2:39351760 | T | A | 1 | a0001c0002t0009g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.245+4489A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39351760 | |||||||
| chr2:39351842 | G | T | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.245+4407C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39351842 | |||||||
| chr2:39351852 | T | C | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.245+4397A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39351852 | |||||||
| chr2:39351859 | G | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.245+4390C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39351859 | |||||||
| chr2:39351999 | G | C | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.245+4250C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39351999 | |||||||
| chr2:39352082 | G | A | 1 | a0001c0003t0004g0228 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.245+4167C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39352082 | |||||||
| chr2:39352096 | G | T | 5 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(2): Show |
5 | HG01496.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.245+4153C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39352096 | |||||||
| chr2:39352159 | C | T | 1 | a0001c0002t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.245+4090G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39352159 | |||||||
| chr2:39352164 | G | A | 1 | a0001c0001t0002g0025 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.245+4085C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39352164 | |||||||
| chr2:39352184 | G | A | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.245+4065C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39352184 | |||||||
| chr2:39352327 | C | T | 5 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(2): Show |
5 | HG01496.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.245+3922G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39352327 | |||||||
| chr2:39352350 | C | A | 1 | a0001c0001t0002g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.245+3899G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39352350 | |||||||
| chr2:39352431 | T | C | 1 | a0001c0003t0004g0217 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.245+3818A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39352431 | |||||||
| chr2:39352584 | A | G | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.245+3665T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39352584 | |||||||
| chr2:39352728 | G | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.245+3521C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39352728 | |||||||
| chr2:39352753 | G | T | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.245+3496C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39352753 | |||||||
| chr2:39352913 | TAGAA | T | 18 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(15): Show |
18 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.245+3332_245+3335d others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39352913 | |||||||
| chr2:39353068 | T | C | 24 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(21): Show |
24 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.245+3181A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39353068 | |||||||
| chr2:39353236 | G | A | 105 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(102): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.245+3013C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39353236 | |||||||
| chr2:39353395 | A | T | 3 | a0001c0003t0005g0005 a0001c0003t0005g0006 a0001c0003t0012g0004 |
3 | HG01884.hp1 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.245+2854T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39353395 | |||||||
| chr2:39353427 | A | G | 1 | a0001c0004t0013g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.245+2822T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39353427 | |||||||
| chr2:39353724 | A | AAGT | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.245+2522_245+2524d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39353724 | |||||||
| chr2:39353733 | TAGTAGCA others(14): Show |
T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.245+2495_245+2515d others(23): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39353733 | |||||||
| chr2:39353736 | T | C | 1 | a0001c0002t0001g0128 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.245+2513A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39353736 | |||||||
| chr2:39353736 | T | TAGC | 2 | a0001c0002t0001g0075 a0001c0002t0001g0126 |
2 | HG02630.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.245+2510_245+2512d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39353736 | |||||||
| chr2:39353736 | TAGCAGCA others(8): Show |
T | 4 | a0001c0002t0001g0095 a0001c0002t0001g0096 a0001c0002t0001g0113 others(1): Show |
4 | HG00280.hp2 HG01109.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+2498_245+2512d others(17): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39353736 | |||||||
| chr2:39353768 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.245+2481T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39353768 | |||||||
| chr2:39353841 | C | T | 1 | a0001c0002t0007g0230 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.245+2408G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39353841 | |||||||
| chr2:39353904 | T | C | 6 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(3): Show |
6 | HG01496.hp1 HG02717.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+2345A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39353904 | |||||||
| chr2:39354166 | A | G | 172 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(169): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.245+2083T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39354166 | |||||||
| chr2:39354270 | C | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245+1979G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39354270 | |||||||
| chr2:39354300 | C | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245+1949G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39354300 | |||||||
| chr2:39354367 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.245+1882G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39354367 | |||||||
| chr2:39354397 | C | A | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245+1852G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39354397 | |||||||
| chr2:39354397 | C | T | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.245+1852G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39354397 | |||||||
| chr2:39354445 | A | AAAAT | 10 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(7): Show |
10 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.245+1800_245+1803d others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39354445 | |||||||
| chr2:39354487 | G | A | 1 | a0001c0002t0001g0047 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.245+1762C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39354487 | |||||||
| chr2:39354518 | T | C | 116 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(113): Show |
116 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.245+1731A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39354518 | |||||||
| chr2:39354655 | C | CT | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245+1593dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39354655 | |||||||
| chr2:39354673 | CA | C | 22 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(19): Show |
22 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.245+1575delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39354673 | |||||||
| chr2:39354677 | A | C | 24 | a0001c0001t0001g0180 a0001c0001t0002g0135 a0001c0001t0003g0032 others(21): Show |
24 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.245+1572T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39354677 | |||||||
| chr2:39354684 | C | A | 1 | a0001c0001t0002g0156 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.245+1565G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39354684 | |||||||
| chr2:39354902 | T | C | 8 | a0001c0001t0002g0042 a0001c0001t0002g0097 a0001c0001t0002g0098 others(5): Show |
8 | HG00741.hp1 HG01081.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.245+1347A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39354902 | |||||||
| chr2:39355059 | T | C | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.245+1190A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355059 | |||||||
| chr2:39355222 | G | A | 1 | a0001c0002t0001g0151 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.245+1027C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355222 | |||||||
| chr2:39355259 | G | A | 1 | a0001c0002t0001g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.245+990C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355259 | |||||||
| chr2:39355278 | T | A | 3 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0055 |
3 | NA18998.hp2 NA19012.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.245+971A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355278 | |||||||
| chr2:39355303 | G | A | 1 | a0001c0002t0001g0115 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.245+946C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355303 | |||||||
| chr2:39355359 | C | CA | 50 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(47): Show |
50 | HG00140.hp1 HG00408.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.245+889dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355359 | |||||||
| chr2:39355359 | C | CAA | 24 | a0001c0001t0001g0180 a0001c0001t0002g0035 a0001c0001t0002g0036 others(21): Show |
24 | HG01099.hp2 HG01243.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.245+888_245+889dup others(2): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355359 | |||||||
| chr2:39355359 | C | CAAA | 7 | a0001c0001t0002g0027 a0001c0001t0003g0186 a0001c0001t0003g0191 others(4): Show |
7 | HG02055.hp2 HG02145.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.245+887_245+889dup others(3): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355359 | |||||||
| chr2:39355359 | CA | C | 5 | a0001c0002t0001g0059 a0001c0003t0005g0005 a0001c0003t0005g0006 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.245+889delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355359 | |||||||
| chr2:39355493 | C | T | 1 | a0001c0001t0002g0025 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.245+756G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355493 | |||||||
| chr2:39355507 | G | A | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245+742C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355507 | |||||||
| chr2:39355533 | C | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245+716G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355533 | |||||||
| chr2:39355769 | AG | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.245+479delC | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355769 | |||||||
| chr2:39355772 | A | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.245+477T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355772 | |||||||
| chr2:39355829 | A | G | 1 | a0001c0002t0009g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245+420T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355829 | |||||||
| chr2:39355831 | G | A | 1 | a0001c0002t0001g0127 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.245+418C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355831 | |||||||
| chr2:39355833 | A | G | 2 | a0001c0002t0001g0062 a0001c0002t0001g0065 |
2 | NA18982.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.245+416T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355833 | |||||||
| chr2:39355931 | C | A | 3 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0055 |
3 | NA18998.hp2 NA19012.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.245+318G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39355931 | |||||||
| chr2:39356093 | T | C | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.245+156A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 3/33 | chr2 | 39356093 | |||||||
| chr2:39356530 | T | C | 2 | a0001c0002t0009g0129 a0001c0003t0004g0218 |
2 | HG00408.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.155-191A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39356530 | |||||||
| chr2:39356557 | T | C | 22 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.155-218A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39356557 | |||||||
| chr2:39356657 | G | C | 1 | a0001c0001t0005g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.155-318C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39356657 | |||||||
| chr2:39356855 | A | G | 3 | a0001c0003t0005g0005 a0001c0003t0005g0006 a0001c0003t0011g0001 |
3 | HG01884.hp1 HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.155-516T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39356855 | |||||||
| chr2:39356882 | T | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.155-543A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39356882 | |||||||
| chr2:39357367 | A | G | 3 | a0001c0001t0003g0188 a0001c0001t0003g0190 a0001c0001t0014g0189 |
3 | HG01243.hp2 HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.155-1028T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39357367 | |||||||
| chr2:39357439 | C | T | 1 | a0001c0002t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.155-1100G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39357439 | |||||||
| chr2:39357681 | T | C | 2 | a0001c0003t0004g0225 a0001c0003t0004g0226 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.155-1342A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39357681 | |||||||
| chr2:39357728 | T | C | 1 | a0001c0001t0003g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.155-1389A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39357728 | |||||||
| chr2:39357909 | A | C | 1 | a0001c0002t0001g0127 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.155-1570T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39357909 | |||||||
| chr2:39358005 | G | A | 1 | a0001c0002t0001g0127 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.155-1666C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39358005 | |||||||
| chr2:39358094 | T | C | 3 | a0001c0002t0001g0131 a0001c0002t0001g0132 a0001c0002t0001g0151 |
3 | HG03831.hp1 HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.155-1755A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39358094 | |||||||
| chr2:39358108 | T | C | 1 | a0001c0002t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.155-1769A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39358108 | |||||||
| chr2:39358224 | G | T | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.155-1885C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39358224 | |||||||
| chr2:39358340 | T | C | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-2001A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39358340 | |||||||
| chr2:39358825 | C | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.155-2486G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39358825 | |||||||
| chr2:39359089 | A | G | 1 | a0001c0002t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.155-2750T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39359089 | |||||||
| chr2:39359123 | C | T | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.155-2784G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39359123 | |||||||
| chr2:39359149 | T | C | 1 | a0001c0001t0003g0206 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.155-2810A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39359149 | |||||||
| chr2:39359162 | G | T | 23 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(20): Show |
23 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.155-2823C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39359162 | |||||||
| chr2:39359164 | T | C | 1 | a0001c0001t0006g0199 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.155-2825A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39359164 | |||||||
| chr2:39359233 | ATAGTCAT others(32): Show |
A | 1 | a0001c0002t0001g0080 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.155-2933_155-2895d others(41): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39359233 | |||||||
| chr2:39359285 | C | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.155-2946G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39359285 | |||||||
| chr2:39359481 | G | C | 91 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.155-3142C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39359481 | |||||||
| chr2:39359611 | G | A | 6 | a0001c0003t0004g0214 a0001c0003t0004g0217 a0001c0003t0004g0218 others(3): Show |
6 | HG00408.hp1 NA18954.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-3272C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39359611 | |||||||
| chr2:39359725 | A | G | 172 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(169): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.155-3386T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39359725 | |||||||
| chr2:39359799 | C | A | 1 | a0001c0003t0004g0222 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.155-3460G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39359799 | |||||||
| chr2:39359881 | G | A | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.155-3542C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39359881 | |||||||
| chr2:39359955 | T | C | 1 | a0001c0002t0001g0076 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.155-3616A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39359955 | |||||||
| chr2:39360218 | C | T | 8 | a0001c0001t0002g0157 a0001c0001t0002g0165 a0001c0001t0002g0167 others(5): Show |
8 | HG02717.hp2 HG03139.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.155-3879G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39360218 | |||||||
| chr2:39360344 | A | G | 13 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(10): Show |
13 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.155-4005T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39360344 | |||||||
| chr2:39360664 | G | A | 18 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(15): Show |
18 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.155-4325C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39360664 | |||||||
| chr2:39360695 | G | T | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.155-4356C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39360695 | |||||||
| chr2:39360722 | A | G | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.155-4383T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39360722 | |||||||
| chr2:39360860 | C | T | 1 | a0001c0002t0001g0085 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.155-4521G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39360860 | |||||||
| chr2:39360910 | G | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.155-4571C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39360910 | |||||||
| chr2:39360929 | A | G | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.155-4590T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39360929 | |||||||
| chr2:39361028 | A | C | 32 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(29): Show |
32 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.155-4689T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39361028 | |||||||
| chr2:39361054 | G | C | 1 | a0001c0002t0001g0072 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.155-4715C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39361054 | |||||||
| chr2:39361131 | T | C | 10 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.155-4792A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39361131 | |||||||
| chr2:39361145 | C | T | 5 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(2): Show |
5 | HG01496.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-4806G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39361145 | |||||||
| chr2:39361248 | TATG | T | 6 | a0001c0001t0003g0173 a0001c0001t0003g0181 a0001c0001t0003g0186 others(3): Show |
6 | HG02055.hp2 HG02895.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-4912_155-4910d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39361248 | |||||||
| chr2:39361264 | T | C | 3 | a0001c0002t0001g0057 a0001c0002t0001g0074 a0001c0002t0001g0125 |
3 | HG00408.hp2 HG01934.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.155-4925A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39361264 | |||||||
| chr2:39361359 | ATG | A | 2 | a0001c0002t0001g0066 a0001c0002t0001g0092 |
2 | NA18952.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.155-5022_155-5021d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39361359 | |||||||
| chr2:39361473 | T | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.155-5134A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39361473 | |||||||
| chr2:39361629 | T | C | 8 | a0001c0001t0003g0173 a0001c0001t0003g0181 a0001c0001t0003g0186 others(5): Show |
8 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-5290A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39361629 | |||||||
| chr2:39361656 | T | C | 131 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(128): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.155-5317A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39361656 | |||||||
| chr2:39361800 | A | C | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.155-5461T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39361800 | |||||||
| chr2:39361974 | A | T | 2 | a0001c0001t0003g0176 a0001c0001t0003g0177 |
2 | HG01099.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.155-5635T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39361974 | |||||||
| chr2:39362072 | T | C | 1 | a0001c0001t0006g0205 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.155-5733A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39362072 | |||||||
| chr2:39362147 | T | C | 90 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.155-5808A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39362147 | |||||||
| chr2:39362558 | A | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.155-6219T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39362558 | |||||||
| chr2:39362937 | T | G | 1 | a0001c0003t0002g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.155-6598A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39362937 | |||||||
| chr2:39363272 | G | A | 1 | a0001c0002t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.155-6933C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39363272 | |||||||
| chr2:39363299 | T | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.155-6960A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39363299 | |||||||
| chr2:39363307 | A | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.155-6968T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39363307 | |||||||
| chr2:39363396 | AGTGG | A | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.155-7061_155-7058d others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39363396 | |||||||
| chr2:39363582 | T | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.155-7243A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39363582 | |||||||
| chr2:39363606 | T | C | 1 | a0001c0002t0001g0074 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.155-7267A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39363606 | |||||||
| chr2:39363668 | C | CA | 30 | a0001c0001t0001g0180 a0001c0001t0002g0139 a0001c0001t0002g0141 others(27): Show |
30 | HG01099.hp2 HG01106.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.155-7330dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39363668 | |||||||
| chr2:39363668 | C | CAA | 81 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(78): Show |
81 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.155-7331_155-7330d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39363668 | |||||||
| chr2:39363668 | C | CAAA | 8 | a0001c0002t0001g0059 a0001c0002t0001g0063 a0001c0002t0001g0085 others(5): Show |
8 | HG01934.hp2 HG02129.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-7332_155-7330d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39363668 | |||||||
| chr2:39363684 | A | G | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.155-7345T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39363684 | |||||||
| chr2:39363862 | C | G | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.155-7523G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39363862 | |||||||
| chr2:39363885 | T | C | 1 | a0001c0002t0001g0128 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.155-7546A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39363885 | |||||||
| chr2:39363992 | T | TA | 129 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(126): Show |
129 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.155-7654dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39363992 | |||||||
| chr2:39363992 | TA | T | 36 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(33): Show |
36 | HG00609.hp1 HG00741.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.155-7654delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39363992 | |||||||
| chr2:39364010 | A | G | 10 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.155-7671T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39364010 | |||||||
| chr2:39364206 | T | G | 3 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0163 |
3 | HG01106.hp2 HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.155-7867A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39364206 | |||||||
| chr2:39364499 | C | G | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.155-8160G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39364499 | |||||||
| chr2:39364575 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.155-8236G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39364575 | |||||||
| chr2:39364865 | C | CA | 95 | a0001c0001t0002g0139 a0001c0001t0003g0175 a0001c0001t0003g0176 others(92): Show |
95 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.155-8527dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39364865 | |||||||
| chr2:39364865 | C | CAA | 21 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(18): Show |
21 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.155-8528_155-8527d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39364865 | |||||||
| chr2:39364865 | CA | C | 11 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0109 others(8): Show |
11 | HG01255.hp1 HG02895.hp1 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.155-8527delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39364865 | |||||||
| chr2:39365103 | T | C | 3 | a0001c0002t0001g0131 a0001c0002t0001g0132 a0001c0002t0001g0151 |
3 | HG03831.hp1 HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.155-8764A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39365103 | |||||||
| chr2:39365259 | T | C | 172 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(169): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.155-8920A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39365259 | |||||||
| chr2:39365296 | G | A | 2 | a0001c0001t0002g0035 a0001c0002t0001g0075 |
2 | HG03486.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.155-8957C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39365296 | |||||||
| chr2:39365319 | T | A | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.155-8980A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39365319 | |||||||
| chr2:39365361 | T | A | 1 | a0001c0001t0002g0019 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.155-9022A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39365361 | |||||||
| chr2:39365421 | G | A | 1 | a0001c0001t0002g0116 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.155-9082C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39365421 | |||||||
| chr2:39365428 | T | A | 1 | a0001c0001t0002g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.155-9089A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39365428 | |||||||
| chr2:39365428 | T | TA | 87 | a0001c0001t0001g0180 a0001c0001t0002g0028 a0001c0001t0002g0029 others(84): Show |
87 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.155-9090dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39365428 | |||||||
| chr2:39365430 | A | AAT | 34 | a0001c0001t0002g0027 a0001c0001t0002g0035 a0001c0001t0003g0174 others(31): Show |
34 | HG00741.hp2 HG01168.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.155-9092_155-9091i others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39365430 | |||||||
| chr2:39365430 | A | AT | 30 | a0001c0001t0002g0023 a0001c0001t0002g0101 a0001c0001t0002g0106 others(27): Show |
30 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.155-9092dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39365430 | |||||||
| chr2:39365430 | AT | A | 15 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(12): Show |
15 | HG00738.hp1 HG01081.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.155-9092delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39365430 | |||||||
| chr2:39365468 | C | T | 1 | a0001c0001t0002g0136 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.155-9129G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39365468 | |||||||
| chr2:39365893 | C | A | 1 | a0001c0001t0002g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.155-9554G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39365893 | |||||||
| chr2:39365937 | A | T | 3 | a0001c0001t0002g0099 a0001c0001t0002g0109 a0001c0001t0002g0137 |
3 | HG01255.hp1 HG01496.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.155-9598T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39365937 | |||||||
| chr2:39366146 | A | G | 10 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.155-9807T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39366146 | |||||||
| chr2:39366175 | T | A | 1 | a0001c0002t0001g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.155-9836A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39366175 | |||||||
| chr2:39366196 | C | T | 2 | a0001c0001t0005g0015 a0003c0009t0005g0016 |
2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.155-9857G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39366196 | |||||||
| chr2:39366301 | G | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.155-9962C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39366301 | |||||||
| chr2:39366410 | T | C | 1 | a0001c0001t0002g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.155-10071A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39366410 | |||||||
| chr2:39366466 | C | T | 22 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(19): Show |
22 | HG01433.hp2 HG02258.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.155-10127G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39366466 | |||||||
| chr2:39366479 | G | A | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.155-10140C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39366479 | |||||||
| chr2:39366533 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.155-10194G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39366533 | |||||||
| chr2:39366635 | G | A | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-10296C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39366635 | |||||||
| chr2:39366688 | A | T | 1 | a0001c0001t0005g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.155-10349T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39366688 | |||||||
| chr2:39366970 | C | T | 39 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(36): Show |
39 | HG00609.hp1 HG00741.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.155-10631G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39366970 | |||||||
| chr2:39367138 | G | C | 18 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(15): Show |
18 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.155-10799C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39367138 | |||||||
| chr2:39367162 | C | G | 1 | a0001c0002t0001g0146 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.155-10823G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39367162 | |||||||
| chr2:39367438 | G | A | 6 | a0001c0003t0004g0214 a0001c0003t0004g0217 a0001c0003t0004g0218 others(3): Show |
6 | HG00408.hp1 NA18954.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.154+10628C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39367438 | |||||||
| chr2:39367597 | C | T | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.154+10469G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39367597 | |||||||
| chr2:39367665 | G | A | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.154+10401C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39367665 | |||||||
| chr2:39368059 | T | TGA | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+10005_154+1000 others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39368059 | |||||||
| chr2:39368095 | G | A | 23 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(20): Show |
23 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.154+9971C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39368095 | |||||||
| chr2:39368282 | C | A | 1 | a0001c0002t0001g0026 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.154+9784G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39368282 | |||||||
| chr2:39368292 | T | G | 2 | a0001c0002t0001g0081 a0001c0002t0001g0082 |
2 | NA18948.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.154+9774A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39368292 | |||||||
| chr2:39368305 | A | G | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.154+9761T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39368305 | |||||||
| chr2:39368325 | A | T | 173 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(170): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.154+9741T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39368325 | |||||||
| chr2:39368503 | CA | C | 8 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(5): Show |
8 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+9562delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39368503 | |||||||
| chr2:39368736 | C | T | 2 | a0001c0003t0004g0225 a0001c0003t0004g0226 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.154+9330G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39368736 | |||||||
| chr2:39368784 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.154+9282C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39368784 | |||||||
| chr2:39369154 | C | A | 7 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(4): Show |
7 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+8912G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369154 | |||||||
| chr2:39369193 | G | GTTTTTTT others(6): Show |
4 | a0001c0001t0003g0174 a0001c0001t0003g0190 a0001c0001t0014g0189 others(1): Show |
4 | HG02622.hp2 HG02922.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+8872_154+8873i others(15): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369193 | |||||||
| chr2:39369193 | G | GTTTTTTT others(7): Show |
15 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0177 others(12): Show |
15 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.154+8872_154+8873i others(16): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369193 | |||||||
| chr2:39369193 | G | GTTTTTTT others(8): Show |
2 | a0001c0001t0003g0175 a0001c0001t0003g0176 |
2 | HG01099.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.154+8872_154+8873i others(17): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369193 | |||||||
| chr2:39369193 | G | GTTTTTTT others(9): Show |
3 | a0001c0001t0003g0178 a0001c0003t0004g0214 a0001c0003t0004g0229 |
3 | HG02257.hp2 NA18953.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.154+8872_154+8873i others(18): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369193 | |||||||
| chr2:39369193 | G | GTTTTTTT others(10): Show |
10 | a0001c0003t0004g0216 a0001c0003t0004g0218 a0001c0003t0004g0219 others(7): Show |
10 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.154+8872_154+8873i others(19): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369193 | |||||||
| chr2:39369193 | G | GTTTTTTT others(11): Show |
3 | a0001c0003t0004g0217 a0001c0003t0004g0225 a0001c0003t0004g0226 |
3 | HG03490.hp2 HG03492.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.154+8872_154+8873i others(20): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369193 | |||||||
| chr2:39369193 | G | GTTTTTTT others(12): Show |
1 | a0001c0003t0004g0215 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.154+8872_154+8873i others(21): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369193 | |||||||
| chr2:39369193 | G | GTTTTTTT others(5): Show |
1 | a0001c0004t0013g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.154+8872_154+8873i others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369193 | |||||||
| chr2:39369193 | G | GTTTTTTT others(8): Show |
2 | a0001c0001t0006g0198 a0001c0001t0006g0201 |
2 | HG01433.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.154+8872_154+8873i others(17): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369193 | |||||||
| chr2:39369193 | G | GTTTTTTT others(9): Show |
3 | a0001c0001t0006g0200 a0001c0001t0006g0202 a0001c0001t0006g0205 |
3 | NA18981.hp1 NA19070.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.154+8872_154+8873i others(18): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369193 | |||||||
| chr2:39369193 | G | GTTTTTTT others(10): Show |
1 | a0001c0001t0006g0203 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.154+8872_154+8873i others(19): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369193 | |||||||
| chr2:39369193 | G | GTTTTTTT others(11): Show |
2 | a0001c0001t0006g0199 a0001c0001t0006g0204 |
2 | NA18945.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.154+8872_154+8873i others(20): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369193 | |||||||
| chr2:39369198 | T | TTTGTTTG others(8): Show |
1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.154+8867_154+8868i others(17): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369198 | |||||||
| chr2:39369200 | T | TTTTTTGT others(9): Show |
1 | a0001c0002t0001g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.154+8865_154+8866i others(18): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369200 | |||||||
| chr2:39369205 | G | GTTTTTTG others(6): Show |
20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.154+8860_154+8861i others(15): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369205 | |||||||
| chr2:39369205 | G | GTTTTTTT others(9): Show |
2 | a0001c0002t0001g0121 a0001c0002t0001g0149 |
2 | HG02257.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.154+8860_154+8861i others(18): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369205 | |||||||
| chr2:39369205 | G | GTTTTTTT others(8): Show |
3 | a0001c0001t0003g0164 a0001c0001t0003g0169 a0001c0001t0003g0170 |
3 | HG03209.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.154+8860_154+8861i others(17): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369205 | |||||||
| chr2:39369205 | G | GTTTTTTT others(5): Show |
1 | a0001c0004t0005g0002 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.154+8860_154+8861i others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369205 | |||||||
| chr2:39369205 | G | GTTTTTTT others(6): Show |
3 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0005t0002g0033 |
3 | HG01884.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.154+8860_154+8861i others(15): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369205 | |||||||
| chr2:39369205 | G | GTTTTTTT others(7): Show |
50 | a0001c0001t0002g0018 a0001c0001t0002g0020 a0001c0001t0002g0021 others(47): Show |
50 | HG00609.hp1 HG00738.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.154+8860_154+8861i others(16): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369205 | |||||||
| chr2:39369205 | G | GTTTTTTT others(8): Show |
11 | a0001c0001t0002g0019 a0001c0001t0002g0106 a0001c0001t0002g0136 others(8): Show |
11 | HG02630.hp1 HG02717.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.154+8860_154+8861i others(17): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369205 | |||||||
| chr2:39369205 | G | GTTTTTTT others(9): Show |
2 | a0001c0001t0002g0157 a0001c0001t0002g0165 |
2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.154+8860_154+8861i others(18): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369205 | |||||||
| chr2:39369205 | G | T | 50 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(47): Show |
50 | HG00140.hp1 HG00408.hp1 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.154+8861C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369205 | |||||||
| chr2:39369300 | A | G | 38 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(35): Show |
38 | HG00140.hp1 HG00408.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.154+8766T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369300 | |||||||
| chr2:39369383 | C | A | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.154+8683G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369383 | |||||||
| chr2:39369407 | A | G | 2 | a0001c0002t0007g0223 a0001c0002t0007g0224 |
2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.154+8659T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369407 | |||||||
| chr2:39369590 | G | C | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.154+8476C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369590 | |||||||
| chr2:39369665 | C | G | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.154+8401G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369665 | |||||||
| chr2:39369819 | C | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.154+8247G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369819 | |||||||
| chr2:39369887 | C | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+8179G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369887 | |||||||
| chr2:39369990 | T | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.154+8076A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39369990 | |||||||
| chr2:39370189 | T | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+7877A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39370189 | |||||||
| chr2:39370230 | C | G | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+7836G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39370230 | |||||||
| chr2:39370292 | A | G | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+7774T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39370292 | |||||||
| chr2:39370363 | C | T | 172 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(169): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.154+7703G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39370363 | |||||||
| chr2:39370395 | G | C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.154+7671C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39370395 | |||||||
| chr2:39370480 | T | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.154+7586A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39370480 | |||||||
| chr2:39370521 | C | CA | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.154+7544dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39370521 | |||||||
| chr2:39370631 | G | A | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.154+7435C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39370631 | |||||||
| chr2:39370743 | T | C | 1 | a0001c0002t0001g0148 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.154+7323A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39370743 | |||||||
| chr2:39370846 | G | A | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.154+7220C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39370846 | |||||||
| chr2:39370908 | T | C | 1 | a0001c0002t0001g0093 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.154+7158A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39370908 | |||||||
| chr2:39370963 | A | G | 1 | a0001c0002t0001g0146 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.154+7103T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39370963 | |||||||
| chr2:39370967 | A | G | 173 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(170): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.154+7099T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39370967 | |||||||
| chr2:39371028 | T | C | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+7038A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39371028 | |||||||
| chr2:39371094 | C | T | 22 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(19): Show |
22 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.154+6972G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39371094 | |||||||
| chr2:39371167 | T | C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.154+6899A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39371167 | |||||||
| chr2:39371223 | G | A | 2 | a0001c0001t0002g0105 a0001c0001t0002g0139 |
2 | HG01346.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.154+6843C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39371223 | |||||||
| chr2:39371476 | T | A | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.154+6590A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39371476 | |||||||
| chr2:39371481 | G | A | 23 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(20): Show |
23 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.154+6585C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39371481 | |||||||
| chr2:39371813 | A | C | 225 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.154+6253T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39371813 | |||||||
| chr2:39371815 | A | C | 105 | a0001c0001t0001g0180 a0001c0001t0002g0119 a0001c0001t0002g0135 others(102): Show |
105 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.154+6251T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39371815 | |||||||
| chr2:39371893 | T | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.154+6173A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39371893 | |||||||
| chr2:39371898 | A | G | 26 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(23): Show |
26 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.154+6168T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39371898 | |||||||
| chr2:39371980 | G | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+6086C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39371980 | |||||||
| chr2:39371981 | C | G | 173 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(170): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.154+6085G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39371981 | |||||||
| chr2:39372042 | T | C | 91 | a0001c0001t0002g0135 a0001c0002t0001g0026 a0001c0002t0001g0037 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.154+6024A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39372042 | |||||||
| chr2:39372166 | G | A | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.154+5900C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39372166 | |||||||
| chr2:39372233 | AT | A | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.154+5832delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39372233 | |||||||
| chr2:39372487 | C | G | 1 | a0001c0002t0001g0058 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.154+5579G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39372487 | |||||||
| chr2:39372488 | T | A | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.154+5578A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39372488 | |||||||
| chr2:39372507 | A | G | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.154+5559T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39372507 | |||||||
| chr2:39372594 | T | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.154+5472A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39372594 | |||||||
| chr2:39372669 | C | G | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.154+5397G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39372669 | |||||||
| chr2:39372695 | G | A | 2 | a0001c0002t0001g0066 a0001c0002t0001g0092 |
2 | NA18952.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.154+5371C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39372695 | |||||||
| chr2:39372697 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.154+5369G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39372697 | |||||||
| chr2:39372760 | C | T | 6 | a0001c0002t0001g0069 a0001c0002t0001g0071 a0001c0002t0001g0077 others(3): Show |
6 | HG02132.hp1 NA18946.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.154+5306G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39372760 | |||||||
| chr2:39372851 | G | C | 2 | a0001c0003t0011g0001 a0001c0004t0005g0002 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.154+5215C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39372851 | |||||||
| chr2:39373095 | A | G | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.154+4971T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39373095 | |||||||
| chr2:39373188 | G | T | 1 | a0001c0002t0001g0149 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.154+4878C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39373188 | |||||||
| chr2:39373581 | C | T | 123 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(120): Show |
123 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.154+4485G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39373581 | |||||||
| chr2:39373658 | C | A | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.154+4408G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39373658 | |||||||
| chr2:39373809 | G | A | 38 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(35): Show |
38 | HG00609.hp1 HG00741.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.154+4257C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39373809 | |||||||
| chr2:39373811 | G | C | 92 | a0001c0001t0002g0135 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.154+4255C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39373811 | |||||||
| chr2:39373814 | G | T | 3 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0055 |
3 | NA18998.hp2 NA19012.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.154+4252C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39373814 | |||||||
| chr2:39373817 | A | T | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+4249T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39373817 | |||||||
| chr2:39374058 | G | A | 22 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.154+4008C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39374058 | |||||||
| chr2:39374100 | G | A | 1 | a0001c0002t0001g0067 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.154+3966C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39374100 | |||||||
| chr2:39374123 | T | C | 92 | a0001c0001t0002g0135 a0001c0002t0001g0026 a0001c0002t0001g0037 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.154+3943A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39374123 | |||||||
| chr2:39374145 | G | T | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.154+3921C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39374145 | |||||||
| chr2:39374189 | A | C | 172 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(169): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.154+3877T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39374189 | |||||||
| chr2:39374367 | T | C | 1 | a0001c0001t0003g0178 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.154+3699A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39374367 | |||||||
| chr2:39374510 | C | T | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.154+3556G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39374510 | |||||||
| chr2:39374586 | G | T | 1 | a0001c0002t0009g0129 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.154+3480C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39374586 | |||||||
| chr2:39374590 | G | A | 22 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.154+3476C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39374590 | |||||||
| chr2:39374629 | C | G | 4 | a0001c0001t0002g0101 a0001c0001t0002g0104 a0001c0001t0002g0108 others(1): Show |
4 | HG00609.hp1 NA18995.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+3437G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39374629 | |||||||
| chr2:39374664 | A | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.154+3402T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39374664 | |||||||
| chr2:39374748 | G | T | 1 | a0001c0002t0001g0128 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.154+3318C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39374748 | |||||||
| chr2:39375142 | C | G | 1 | a0001c0001t0003g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.154+2924G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39375142 | |||||||
| chr2:39375214 | C | T | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.154+2852G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39375214 | |||||||
| chr2:39375368 | A | G | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.154+2698T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39375368 | |||||||
| chr2:39375435 | TG | T | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+2630delC | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39375435 | |||||||
| chr2:39375534 | G | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.154+2532C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39375534 | |||||||
| chr2:39375575 | C | G | 22 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(19): Show |
22 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.154+2491G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39375575 | |||||||
| chr2:39375809 | T | C | 23 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(20): Show |
23 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.154+2257A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39375809 | |||||||
| chr2:39375864 | T | C | 3 | a0001c0002t0001g0144 a0001c0002t0001g0193 a0001c0003t0002g0091 |
3 | HG01952.hp2 HG01978.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.154+2202A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39375864 | |||||||
| chr2:39375877 | G | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+2189C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39375877 | |||||||
| chr2:39376022 | T | C | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.154+2044A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39376022 | |||||||
| chr2:39376048 | CATT | C | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.154+2015_154+2017d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39376048 | |||||||
| chr2:39376288 | G | A | 3 | a0001c0002t0001g0084 a0001c0002t0001g0127 a0001c0002t0001g0133 |
3 | HG01975.hp1 HG01978.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.154+1778C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39376288 | |||||||
| chr2:39376565 | T | A | 1 | a0001c0003t0004g0214 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.154+1501A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39376565 | |||||||
| chr2:39376629 | G | C | 1 | a0003c0009t0005g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.154+1437C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39376629 | |||||||
| chr2:39376630 | C | A | 1 | a0001c0003t0004g0222 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.154+1436G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39376630 | |||||||
| chr2:39376634 | T | A | 1 | a0001c0001t0003g0182 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.154+1432A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39376634 | |||||||
| chr2:39376661 | G | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.154+1405C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39376661 | |||||||
| chr2:39376874 | C | T | 2 | a0001c0002t0001g0112 a0001c0002t0001g0115 |
2 | HG03017.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.154+1192G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39376874 | |||||||
| chr2:39376952 | C | T | 172 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(169): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.154+1114G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39376952 | |||||||
| chr2:39377063 | T | C | 1 | a0001c0002t0001g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.154+1003A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39377063 | |||||||
| chr2:39377099 | T | C | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.154+967A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39377099 | |||||||
| chr2:39377201 | C | CTTTTTTT others(3): Show |
20 | a0001c0002t0001g0026 a0001c0002t0001g0040 a0001c0002t0001g0062 others(17): Show |
20 | HG00140.hp2 HG01106.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.154+855_154+864dup others(10): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39377201 | |||||||
| chr2:39377201 | C | CTTTTTTT others(4): Show |
36 | a0001c0001t0002g0135 a0001c0001t0005g0013 a0001c0002t0001g0037 others(33): Show |
36 | HG00408.hp2 HG00609.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.154+854_154+864dup others(11): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39377201 | |||||||
| chr2:39377201 | C | CTTTTTTT others(5): Show |
54 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(51): Show |
54 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.154+853_154+864dup others(12): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39377201 | |||||||
| chr2:39377201 | C | CTTTTTTT others(6): Show |
1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.154+852_154+864dup others(13): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39377201 | |||||||
| chr2:39377201 | CT | C | 11 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(8): Show |
11 | HG01433.hp2 HG02895.hp1 HG03453.hp2 others(8): Show |
intron_variant | MODIFIER | c.154+864delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39377201 | |||||||
| chr2:39377215 | T | TTTTTTTT others(8): Show |
1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.154+850_154+851ins others(15): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39377215 | |||||||
| chr2:39377219 | C | A | 1 | a0001c0001t0003g0175 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.154+847G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39377219 | |||||||
| chr2:39377726 | G | C | 39 | a0001c0001t0001g0180 a0001c0001t0002g0172 a0001c0001t0003g0173 others(36): Show |
39 | HG00140.hp1 HG00408.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.154+340C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39377726 | |||||||
| chr2:39377735 | A | G | 91 | a0001c0001t0002g0135 a0001c0002t0001g0026 a0001c0002t0001g0037 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.154+331T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39377735 | |||||||
| chr2:39377841 | G | A | 2 | a0001c0003t0004g0228 a0001c0003t0004g0229 |
2 | NA18953.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.154+225C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | 39377841 | |||||||
| chr2:39378295 | T | A | 11 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(8): Show |
11 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-172A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39378295 | |||||||
| chr2:39378400 | T | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97-277A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39378400 | |||||||
| chr2:39378534 | T | C | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.97-411A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39378534 | |||||||
| chr2:39378578 | T | C | 1 | a0001c0001t0002g0023 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.97-455A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39378578 | |||||||
| chr2:39378668 | T | A | 1 | a0001c0002t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.97-545A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39378668 | |||||||
| chr2:39378776 | T | C | 140 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(137): Show |
140 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.97-653A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39378776 | |||||||
| chr2:39378824 | C | G | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.97-701G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39378824 | |||||||
| chr2:39379348 | A | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97-1225T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39379348 | |||||||
| chr2:39379383 | T | A | 1 | a0001c0001t0003g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.97-1260A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39379383 | |||||||
| chr2:39379558 | C | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.97-1435G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39379558 | |||||||
| chr2:39379836 | G | T | 1 | a0001c0001t0005g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.97-1713C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39379836 | |||||||
| chr2:39379942 | T | A | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-1819A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39379942 | |||||||
| chr2:39379966 | C | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.97-1843G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39379966 | |||||||
| chr2:39380084 | C | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.97-1961G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39380084 | |||||||
| chr2:39380632 | G | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-2509C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39380632 | |||||||
| chr2:39380724 | T | G | 1 | a0001c0002t0001g0073 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.97-2601A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39380724 | |||||||
| chr2:39380835 | T | C | 190 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.97-2712A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39380835 | |||||||
| chr2:39380960 | G | A | 3 | a0001c0002t0001g0145 a0001c0002t0001g0146 a0001c0002t0001g0147 |
3 | HG01168.hp1 HG03704.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.97-2837C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39380960 | |||||||
| chr2:39381007 | T | C | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.97-2884A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381007 | |||||||
| chr2:39381011 | C | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.97-2888G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381011 | |||||||
| chr2:39381022 | T | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.97-2899A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381022 | |||||||
| chr2:39381053 | A | C | 1 | a0001c0001t0003g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.97-2930T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381053 | |||||||
| chr2:39381285 | A | T | 3 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0055 |
3 | NA18998.hp2 NA19012.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.97-3162T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381285 | |||||||
| chr2:39381310 | T | C | 32 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(29): Show |
32 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.97-3187A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381310 | |||||||
| chr2:39381356 | A | C | 1 | a0001c0002t0001g0138 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.97-3233T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381356 | |||||||
| chr2:39381443 | T | G | 1 | a0001c0002t0001g0151 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.97-3320A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381443 | |||||||
| chr2:39381547 | T | C | 130 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.97-3424A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381547 | |||||||
| chr2:39381583 | A | AT | 47 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(44): Show |
47 | HG00408.hp1 HG01099.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.97-3461dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381583 | |||||||
| chr2:39381583 | AT | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-3461delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381583 | |||||||
| chr2:39381592 | T | C | 132 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(129): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.97-3469A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381592 | |||||||
| chr2:39381641 | G | C | 152 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(149): Show |
152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.97-3518C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381641 | |||||||
| chr2:39381692 | T | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-3569A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381692 | |||||||
| chr2:39381901 | C | G | 11 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(8): Show |
11 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-3778G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381901 | |||||||
| chr2:39381954 | C | A | 17 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(14): Show |
17 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.97-3831G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39381954 | |||||||
| chr2:39382008 | C | A | 1 | a0001c0002t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.97-3885G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39382008 | |||||||
| chr2:39382349 | A | G | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.97-4226T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39382349 | |||||||
| chr2:39382397 | C | A | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.97-4274G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39382397 | |||||||
| chr2:39382602 | C | T | 1 | a0001c0002t0001g0082 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.97-4479G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39382602 | |||||||
| chr2:39382628 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-4505A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39382628 | |||||||
| chr2:39382659 | A | C | 6 | a0001c0001t0003g0032 a0001c0001t0003g0182 a0001c0001t0003g0183 others(3): Show |
6 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-4536T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39382659 | |||||||
| chr2:39382808 | T | C | 1 | a0001c0002t0001g0193 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.97-4685A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39382808 | |||||||
| chr2:39382939 | G | A | 24 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(21): Show |
24 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.97-4816C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39382939 | |||||||
| chr2:39383362 | A | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-5239T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39383362 | |||||||
| chr2:39383375 | A | G | 22 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(19): Show |
22 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.97-5252T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39383375 | |||||||
| chr2:39383421 | T | TC | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.97-5299dupG | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39383421 | |||||||
| chr2:39383543 | T | C | 1 | a0001c0002t0001g0193 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.97-5420A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39383543 | |||||||
| chr2:39383636 | A | G | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.97-5513T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39383636 | |||||||
| chr2:39383786 | T | C | 3 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 |
3 | HG02451.hp2 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.97-5663A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39383786 | |||||||
| chr2:39383802 | TAA | T | 22 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.97-5681_97-5680del others(2): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39383802 | |||||||
| chr2:39383835 | T | C | 22 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.97-5712A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39383835 | |||||||
| chr2:39383864 | C | T | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.97-5741G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39383864 | |||||||
| chr2:39383873 | A | G | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-5750T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39383873 | |||||||
| chr2:39383922 | T | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-5799A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39383922 | |||||||
| chr2:39384038 | C | A | 3 | a0001c0001t0006g0199 a0001c0001t0006g0203 a0001c0001t0006g0204 |
3 | NA18945.hp2 NA18952.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.97-5915G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39384038 | |||||||
| chr2:39384112 | T | TA | 25 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0164 others(22): Show |
25 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.97-5990dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39384112 | |||||||
| chr2:39384112 | TA | T | 30 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(27): Show |
30 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.97-5990delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39384112 | |||||||
| chr2:39384134 | T | C | 1 | a0001c0002t0001g0057 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.97-6011A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39384134 | |||||||
| chr2:39384213 | C | T | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.97-6090G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39384213 | |||||||
| chr2:39384241 | T | C | 130 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.97-6118A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39384241 | |||||||
| chr2:39384324 | T | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97-6201A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39384324 | |||||||
| chr2:39384338 | G | C | 1 | a0001c0007t0001g0048 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.97-6215C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39384338 | |||||||
| chr2:39384440 | A | G | 185 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(182): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.97-6317T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39384440 | |||||||
| chr2:39384444 | G | A | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.97-6321C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39384444 | |||||||
| chr2:39384456 | G | C | 130 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.97-6333C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39384456 | |||||||
| chr2:39384726 | G | A | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.97-6603C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39384726 | |||||||
| chr2:39384886 | C | T | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-6763G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39384886 | |||||||
| chr2:39385185 | G | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-7062C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385185 | |||||||
| chr2:39385255 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-7132A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385255 | |||||||
| chr2:39385304 | C | T | 1 | a0001c0002t0010g0213 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.97-7181G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385304 | |||||||
| chr2:39385324 | G | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-7201C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385324 | |||||||
| chr2:39385351 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-7228A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385351 | |||||||
| chr2:39385551 | C | CAT | 11 | a0001c0001t0002g0036 a0001c0001t0002g0099 a0001c0001t0002g0157 others(8): Show |
11 | HG01243.hp1 HG01243.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-7430_97-7429dup others(2): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | C | CATAT | 12 | a0001c0001t0002g0143 a0001c0001t0002g0152 a0001c0001t0002g0153 others(9): Show |
12 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-7432_97-7429dup others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | C | CATATAT | 20 | a0001c0001t0001g0180 a0001c0001t0002g0020 a0001c0001t0002g0021 others(17): Show |
20 | HG01433.hp2 HG01884.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.97-7434_97-7429dup others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | C | CATATATA others(1): Show |
14 | a0001c0001t0002g0019 a0001c0001t0002g0025 a0001c0001t0002g0035 others(11): Show |
14 | HG00408.hp1 HG02132.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-7436_97-7429dup others(8): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | C | CATATATA others(3): Show |
11 | a0001c0001t0002g0018 a0001c0001t0002g0045 a0001c0001t0002g0101 others(8): Show |
11 | HG00609.hp1 HG01255.hp1 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-7438_97-7429dup others(10): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | C | CATATATA others(5): Show |
9 | a0001c0001t0002g0042 a0001c0001t0002g0102 a0001c0001t0002g0108 others(6): Show |
9 | HG01167.hp2 HG01358.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.97-7440_97-7429dup others(12): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | C | CATATATA others(7): Show |
5 | a0001c0001t0002g0098 a0001c0001t0002g0104 a0001c0001t0002g0107 others(2): Show |
5 | HG00741.hp1 HG01257.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-7442_97-7429dup others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | C | CATATATA others(9): Show |
3 | a0001c0001t0002g0103 a0001c0003t0004g0225 a0001c0003t0004g0226 |
3 | HG01081.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.97-7444_97-7429dup others(16): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | C | CATATATA others(15): Show |
3 | a0001c0001t0002g0097 a0001c0001t0002g0100 a0001c0001t0003g0182 |
3 | HG01975.hp2 HG02300.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.97-7450_97-7429dup others(22): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | CAT | C | 6 | a0001c0001t0002g0027 a0001c0001t0002g0029 a0001c0001t0002g0141 others(3): Show |
6 | HG01496.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-7430_97-7429del others(2): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | CATAT | C | 2 | a0001c0001t0002g0028 a0003c0009t0005g0016 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.97-7432_97-7429del others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | CATATAT | C | 4 | a0001c0001t0002g0030 a0001c0001t0002g0167 a0001c0001t0002g0168 others(1): Show |
4 | HG03139.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-7434_97-7429del others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | CATATATA others(1): Show |
C | 4 | a0001c0001t0002g0031 a0001c0002t0001g0060 a0001c0002t0001g0061 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-7436_97-7429del others(8): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | CATATATA others(3): Show |
C | 12 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(9): Show |
12 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.97-7438_97-7429del others(10): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | CATATATA others(5): Show |
C | 14 | a0001c0001t0002g0155 a0001c0001t0005g0011 a0001c0001t0005g0012 others(11): Show |
14 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-7440_97-7429del others(12): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | CATATATA others(7): Show |
C | 24 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0057 others(21): Show |
24 | HG00280.hp2 HG00408.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.97-7442_97-7429del others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | CATATATA others(9): Show |
C | 57 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(54): Show |
57 | HG00140.hp1 HG00140.hp2 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.97-7444_97-7429del others(16): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | CATATATA others(11): Show |
C | 4 | a0001c0001t0002g0156 a0001c0002t0001g0086 a0001c0004t0005g0002 others(1): Show |
4 | HG00738.hp2 HG01257.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-7446_97-7429del others(18): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | CATATATA others(15): Show |
C | 1 | a0001c0001t0002g0105 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.97-7450_97-7429del others(22): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | CATATATA others(21): Show |
C | 1 | a0001c0001t0003g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.97-7456_97-7429del others(28): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385551 | CATATATA others(23): Show |
C | 7 | a0001c0001t0003g0173 a0001c0001t0003g0179 a0001c0001t0003g0181 others(4): Show |
7 | HG02055.hp2 HG02895.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-7458_97-7429del others(30): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385551 | |||||||
| chr2:39385583 | T | TATATATA others(3): Show |
1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.97-7461_97-7460ins others(10): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385583 | |||||||
| chr2:39385620 | T | C | 7 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-7497A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385620 | |||||||
| chr2:39385631 | A | AT | 17 | a0001c0001t0015g0192 a0001c0003t0004g0214 a0001c0003t0004g0215 others(14): Show |
17 | HG00408.hp1 HG01934.hp1 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.97-7509dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385631 | |||||||
| chr2:39385652 | G | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-7529C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385652 | |||||||
| chr2:39385738 | T | C | 1 | a0001c0002t0001g0127 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.97-7615A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385738 | |||||||
| chr2:39385797 | T | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-7674A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385797 | |||||||
| chr2:39385993 | T | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-7870A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39385993 | |||||||
| chr2:39386009 | T | A | 4 | a0001c0002t0001g0095 a0001c0002t0001g0096 a0001c0002t0001g0113 others(1): Show |
4 | HG00280.hp2 HG01109.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-7886A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386009 | |||||||
| chr2:39386009 | T | G | 136 | a0001c0001t0001g0180 a0001c0001t0002g0035 a0001c0001t0002g0036 others(133): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.97-7886A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386009 | |||||||
| chr2:39386098 | T | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.97-7975A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386098 | |||||||
| chr2:39386099 | T | A | 7 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-7976A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386099 | |||||||
| chr2:39386126 | C | T | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-8003G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386126 | |||||||
| chr2:39386138 | A | G | 15 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(12): Show |
15 | HG00408.hp1 HG01934.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.97-8015T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386138 | |||||||
| chr2:39386340 | C | A | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.97-8217G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386340 | |||||||
| chr2:39386370 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-8247A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386370 | |||||||
| chr2:39386680 | C | T | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.97-8557G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386680 | |||||||
| chr2:39386737 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.97-8614A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386737 | |||||||
| chr2:39386820 | C | CT | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.97-8698dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386820 | |||||||
| chr2:39386820 | C | CTTT | 152 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(149): Show |
152 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.97-8700_97-8698dup others(3): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386820 | |||||||
| chr2:39386820 | C | CTTTTTTT others(5): Show |
2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-8709_97-8698dup others(12): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386820 | |||||||
| chr2:39386820 | C | CTTTTTTT others(6): Show |
17 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(14): Show |
17 | HG00408.hp1 HG01496.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-8710_97-8698dup others(13): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386820 | |||||||
| chr2:39386820 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0015g0192 a0001c0003t0004g0231 a0004c0006t0004g0220 |
3 | HG02922.hp1 NA18961.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.97-8698_97-8697ins others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386820 | |||||||
| chr2:39386820 | C | CTTTTTTT others(8): Show |
2 | a0001c0003t0011g0001 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.97-8698_97-8697ins others(15): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386820 | |||||||
| chr2:39386820 | C | CTTTTTTT others(9): Show |
2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.97-8698_97-8697ins others(16): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386820 | |||||||
| chr2:39386820 | C | CTTTTTTT others(10): Show |
5 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0203 others(2): Show |
5 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-8698_97-8697ins others(17): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386820 | |||||||
| chr2:39386820 | CT | C | 5 | a0001c0001t0006g0200 a0001c0001t0006g0201 a0001c0001t0006g0202 others(2): Show |
5 | HG03490.hp2 HG03492.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-8698delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386820 | |||||||
| chr2:39386959 | G | A | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.97-8836C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386959 | |||||||
| chr2:39386959 | G | T | 57 | a0001c0002t0001g0026 a0001c0002t0001g0037 a0001c0002t0001g0038 others(54): Show |
57 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.97-8836C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39386959 | |||||||
| chr2:39387091 | G | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-8968C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39387091 | |||||||
| chr2:39387113 | G | A | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97-8990C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39387113 | |||||||
| chr2:39387116 | C | T | 1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.97-8993G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39387116 | |||||||
| chr2:39387133 | T | C | 3 | a0001c0001t0003g0164 a0001c0001t0003g0169 a0001c0001t0003g0170 |
3 | HG03209.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.97-9010A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39387133 | |||||||
| chr2:39387256 | T | TA | 16 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(13): Show |
16 | HG01243.hp1 HG01433.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.97-9134dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39387256 | |||||||
| chr2:39387442 | C | T | 1 | a0001c0001t0016g0212 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.97-9319G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39387442 | |||||||
| chr2:39387650 | C | T | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-9527G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39387650 | |||||||
| chr2:39387822 | T | C | 156 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(153): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.97-9699A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39387822 | |||||||
| chr2:39387895 | A | T | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.97-9772T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39387895 | |||||||
| chr2:39387943 | A | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.97-9820T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39387943 | |||||||
| chr2:39387948 | A | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-9825T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39387948 | |||||||
| chr2:39387991 | A | G | 1 | a0001c0002t0001g0071 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.97-9868T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39387991 | |||||||
| chr2:39388110 | A | G | 155 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(152): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.97-9987T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39388110 | |||||||
| chr2:39388154 | T | G | 15 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(12): Show |
15 | HG00408.hp1 HG01934.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.97-10031A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39388154 | |||||||
| chr2:39388213 | G | A | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-10090C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39388213 | |||||||
| chr2:39388377 | C | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-10254G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39388377 | |||||||
| chr2:39388735 | T | G | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.97-10612A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39388735 | |||||||
| chr2:39388772 | A | G | 22 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.97-10649T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39388772 | |||||||
| chr2:39388791 | G | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-10668C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39388791 | |||||||
| chr2:39388888 | C | A | 174 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(171): Show |
174 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.97-10765G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39388888 | |||||||
| chr2:39388908 | G | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-10785C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39388908 | |||||||
| chr2:39389084 | C | T | 6 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0002t0001g0146 others(3): Show |
6 | HG00741.hp2 HG01168.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-10961G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39389084 | |||||||
| chr2:39389212 | C | T | 209 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(206): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.97-11089G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39389212 | |||||||
| chr2:39389311 | G | C | 129 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(126): Show |
129 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.97-11188C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39389311 | |||||||
| chr2:39389490 | C | T | 2 | a0001c0002t0001g0060 a0001c0002t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.97-11367G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39389490 | |||||||
| chr2:39389494 | A | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.97-11371T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39389494 | |||||||
| chr2:39389684 | T | C | 6 | a0001c0001t0005g0008 a0001c0001t0005g0009 a0001c0001t0005g0011 others(3): Show |
6 | HG02258.hp2 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-11561A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39389684 | |||||||
| chr2:39389907 | A | G | 1 | a0001c0003t0004g0219 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.97-11784T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39389907 | |||||||
| chr2:39389990 | T | C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.97-11867A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39389990 | |||||||
| chr2:39390316 | C | T | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97-12193G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39390316 | |||||||
| chr2:39390328 | T | A | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.97-12205A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39390328 | |||||||
| chr2:39390619 | C | G | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-12496G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39390619 | |||||||
| chr2:39390651 | G | C | 1 | a0001c0001t0005g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.97-12528C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39390651 | |||||||
| chr2:39390700 | C | T | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.97-12577G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39390700 | |||||||
| chr2:39390705 | G | T | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.97-12582C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39390705 | |||||||
| chr2:39390772 | TA | T | 190 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(187): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.97-12650delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39390772 | |||||||
| chr2:39390772 | TAA | T | 17 | a0001c0001t0006g0203 a0001c0002t0001g0086 a0001c0003t0004g0214 others(14): Show |
17 | HG00140.hp1 HG00408.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-12651_97-12650d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39390772 | |||||||
| chr2:39390834 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.97-12711C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39390834 | |||||||
| chr2:39390960 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-12837A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39390960 | |||||||
| chr2:39391118 | G | C | 3 | a0001c0001t0002g0106 a0001c0001t0002g0140 a0001c0001t0002g0141 |
3 | NA18945.hp1 NA18946.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.97-12995C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391118 | |||||||
| chr2:39391191 | T | TA | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.97-13069dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391191 | |||||||
| chr2:39391218 | G | C | 3 | a0001c0001t0003g0164 a0001c0001t0003g0169 a0001c0001t0003g0170 |
3 | HG03209.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.97-13095C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391218 | |||||||
| chr2:39391251 | C | T | 18 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0095 others(15): Show |
18 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.97-13128G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391251 | |||||||
| chr2:39391272 | T | C | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.97-13149A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391272 | |||||||
| chr2:39391301 | G | C | 2 | a0001c0002t0001g0039 a0001c0002t0001g0085 |
2 | NA18981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.97-13178C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391301 | |||||||
| chr2:39391312 | T | C | 17 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(14): Show |
17 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-13189A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391312 | |||||||
| chr2:39391358 | C | CA | 43 | a0001c0001t0001g0180 a0001c0001t0002g0030 a0001c0001t0002g0031 others(40): Show |
43 | HG00280.hp1 HG00738.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.97-13236dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391358 | |||||||
| chr2:39391358 | C | CAA | 24 | a0001c0001t0003g0186 a0001c0001t0005g0008 a0001c0001t0008g0051 others(21): Show |
24 | HG00140.hp1 HG00408.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.97-13237_97-13236d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391358 | |||||||
| chr2:39391358 | C | CAAA | 60 | a0001c0001t0002g0123 a0001c0002t0001g0026 a0001c0002t0001g0037 others(57): Show |
60 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.97-13238_97-13236d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391358 | |||||||
| chr2:39391358 | C | CAAAA | 65 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(62): Show |
65 | HG00280.hp2 HG00609.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.97-13239_97-13236d others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391358 | |||||||
| chr2:39391378 | A | AG | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.97-13256_97-13255i others(3): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391378 | |||||||
| chr2:39391394 | G | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-13271C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391394 | |||||||
| chr2:39391525 | G | A | 152 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(149): Show |
152 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.97-13402C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391525 | |||||||
| chr2:39391528 | C | A | 1 | a0001c0002t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.97-13405G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391528 | |||||||
| chr2:39391590 | A | G | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97-13467T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391590 | |||||||
| chr2:39391770 | G | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.97-13647C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391770 | |||||||
| chr2:39391793 | T | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-13670A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391793 | |||||||
| chr2:39391808 | C | T | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.97-13685G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391808 | |||||||
| chr2:39391874 | G | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.97-13751C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391874 | |||||||
| chr2:39391975 | G | A | 1 | a0001c0003t0004g0228 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.97-13852C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391975 | |||||||
| chr2:39391988 | C | A | 22 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(19): Show |
22 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.97-13865G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391988 | |||||||
| chr2:39391998 | C | T | 1 | a0001c0002t0001g0128 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.97-13875G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39391998 | |||||||
| chr2:39392026 | C | A | 1 | a0001c0003t0005g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-13903G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392026 | |||||||
| chr2:39392183 | C | CAAA | 129 | a0001c0001t0001g0180 a0001c0001t0002g0019 a0001c0001t0002g0020 others(126): Show |
129 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.97-14063_97-14061d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392183 | |||||||
| chr2:39392183 | C | CAAAA | 19 | a0001c0001t0002g0018 a0001c0001t0002g0042 a0001c0001t0002g0102 others(16): Show |
19 | HG01081.hp2 HG01167.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.97-14064_97-14061d others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392183 | |||||||
| chr2:39392183 | C | CAAAAAA | 13 | a0001c0001t0002g0053 a0001c0001t0002g0055 a0001c0001t0002g0056 others(10): Show |
13 | HG01168.hp2 HG01169.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-14066_97-14061d others(8): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392183 | |||||||
| chr2:39392183 | C | CAAAAAAA | 8 | a0001c0001t0002g0052 a0001c0001t0002g0054 a0001c0001t0005g0009 others(5): Show |
8 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.97-14067_97-14061d others(9): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392183 | |||||||
| chr2:39392183 | C | CAAAAAAA others(3): Show |
1 | a0001c0003t0005g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-14070_97-14061d others(12): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392183 | |||||||
| chr2:39392183 | C | CAAAAAAA others(5): Show |
2 | a0001c0003t0004g0225 a0001c0003t0004g0226 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.97-14072_97-14061d others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392183 | |||||||
| chr2:39392183 | C | CAAAAAAA others(6): Show |
8 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(5): Show |
8 | HG00140.hp1 HG02129.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-14073_97-14061d others(15): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392183 | |||||||
| chr2:39392183 | C | CAAAAAAA others(7): Show |
5 | a0001c0003t0004g0217 a0001c0003t0004g0222 a0001c0003t0004g0229 others(2): Show |
5 | HG01934.hp1 NA18953.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-14074_97-14061d others(16): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392183 | |||||||
| chr2:39392183 | C | CAAAAAAA others(8): Show |
1 | a0001c0003t0004g0218 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.97-14075_97-14061d others(17): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392183 | |||||||
| chr2:39392183 | C | CAAAAAAA others(9): Show |
4 | a0001c0001t0006g0198 a0001c0001t0006g0200 a0001c0001t0006g0201 others(1): Show |
4 | HG01433.hp2 NA18965.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-14076_97-14061d others(18): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392183 | |||||||
| chr2:39392183 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0006g0202 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.97-14077_97-14061d others(19): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392183 | |||||||
| chr2:39392183 | C | CAAAAAAA others(11): Show |
3 | a0001c0001t0006g0199 a0001c0001t0006g0203 a0001c0001t0006g0204 |
3 | NA18945.hp2 NA18952.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.97-14078_97-14061d others(20): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392183 | |||||||
| chr2:39392183 | CAAA | C | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0035 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-14063_97-14061d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392183 | |||||||
| chr2:39392317 | G | A | 2 | a0001c0002t0001g0082 a0001c0002t0001g0130 |
2 | NA18960.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.97-14194C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392317 | |||||||
| chr2:39392489 | A | G | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.97-14366T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392489 | |||||||
| chr2:39392604 | T | C | 1 | a0001c0001t0005g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.97-14481A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392604 | |||||||
| chr2:39392670 | A | G | 3 | a0001c0002t0001g0059 a0001c0002t0001g0068 a0001c0002t0009g0041 |
3 | HG02145.hp1 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.97-14547T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392670 | |||||||
| chr2:39392689 | T | C | 7 | a0001c0002t0001g0037 a0001c0002t0001g0057 a0001c0002t0001g0080 others(4): Show |
7 | HG00408.hp2 NA18942.hp2 NA18986.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-14566A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392689 | |||||||
| chr2:39392701 | A | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-14578T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392701 | |||||||
| chr2:39392777 | A | T | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.97-14654T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392777 | |||||||
| chr2:39392872 | C | T | 113 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(110): Show |
113 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.97-14749G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392872 | |||||||
| chr2:39392918 | A | G | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.97-14795T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392918 | |||||||
| chr2:39392952 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-14829A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39392952 | |||||||
| chr2:39393202 | G | A | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.97-15079C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39393202 | |||||||
| chr2:39393385 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-15262A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39393385 | |||||||
| chr2:39393410 | C | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-15287G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39393410 | |||||||
| chr2:39393551 | G | A | 1 | a0001c0002t0001g0130 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.97-15428C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39393551 | |||||||
| chr2:39393553 | G | A | 22 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.97-15430C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39393553 | |||||||
| chr2:39393554 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-15431G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39393554 | |||||||
| chr2:39393700 | G | C | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.97-15577C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39393700 | |||||||
| chr2:39393704 | G | C | 1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.97-15581C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39393704 | |||||||
| chr2:39393848 | A | G | 164 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(161): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.97-15725T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39393848 | |||||||
| chr2:39393936 | T | C | 1 | a0001c0002t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.97-15813A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39393936 | |||||||
| chr2:39393981 | A | G | 1 | a0001c0002t0001g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.97-15858T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39393981 | |||||||
| chr2:39394123 | T | C | 22 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(19): Show |
22 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.97-16000A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39394123 | |||||||
| chr2:39394154 | G | A | 22 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(19): Show |
22 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.97-16031C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39394154 | |||||||
| chr2:39394304 | A | G | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.97-16181T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39394304 | |||||||
| chr2:39394346 | C | G | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-16223G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39394346 | |||||||
| chr2:39394402 | T | C | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0035 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-16279A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39394402 | |||||||
| chr2:39394549 | A | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-16426T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39394549 | |||||||
| chr2:39394596 | C | T | 1 | a0001c0001t0002g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.97-16473G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39394596 | |||||||
| chr2:39394738 | G | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-16615C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39394738 | |||||||
| chr2:39394969 | T | A | 1 | a0001c0001t0002g0054 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.97-16846A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39394969 | |||||||
| chr2:39394997 | G | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-16874C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39394997 | |||||||
| chr2:39395102 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-16979A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39395102 | |||||||
| chr2:39395130 | A | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-17007T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39395130 | |||||||
| chr2:39395240 | G | C | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.97-17117C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39395240 | |||||||
| chr2:39395328 | TAC | T | 78 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(75): Show |
78 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.97-17207_97-17206d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39395328 | |||||||
| chr2:39395328 | TACAC | T | 127 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(124): Show |
127 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.97-17209_97-17206d others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39395328 | |||||||
| chr2:39395328 | TACACAC | T | 7 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0035 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-17211_97-17206d others(8): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39395328 | |||||||
| chr2:39395378 | T | C | 1 | a0001c0002t0001g0076 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.97-17255A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39395378 | |||||||
| chr2:39395695 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-17572G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39395695 | |||||||
| chr2:39395802 | T | C | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.97-17679A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39395802 | |||||||
| chr2:39395884 | G | A | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.97-17761C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39395884 | |||||||
| chr2:39395950 | A | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-17827T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39395950 | |||||||
| chr2:39396128 | C | T | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.97-18005G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396128 | |||||||
| chr2:39396239 | C | A | 92 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.97-18116G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396239 | |||||||
| chr2:39396239 | C | T | 1 | a0001c0001t0002g0140 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.97-18116G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396239 | |||||||
| chr2:39396316 | T | C | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.97-18193A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396316 | |||||||
| chr2:39396350 | G | A | 7 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0035 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-18227C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396350 | |||||||
| chr2:39396454 | A | G | 1 | a0001c0004t0005g0002 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.97-18331T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396454 | |||||||
| chr2:39396478 | A | AT | 7 | a0001c0001t0002g0157 a0001c0001t0002g0171 a0001c0001t0003g0194 others(4): Show |
7 | HG00408.hp2 HG01243.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-18356dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396478 | |||||||
| chr2:39396478 | AT | A | 8 | a0001c0001t0002g0024 a0001c0001t0002g0209 a0001c0002t0001g0046 others(5): Show |
8 | HG02165.hp1 HG02165.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.97-18356delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396478 | |||||||
| chr2:39396498 | T | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-18375A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396498 | |||||||
| chr2:39396518 | C | T | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.97-18395G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396518 | |||||||
| chr2:39396575 | G | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-18452C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396575 | |||||||
| chr2:39396631 | G | A | 1 | a0001c0004t0013g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.97-18508C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396631 | |||||||
| chr2:39396715 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-18592G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396715 | |||||||
| chr2:39396716 | G | A | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.97-18593C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396716 | |||||||
| chr2:39396719 | C | T | 114 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(111): Show |
114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.97-18596G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396719 | |||||||
| chr2:39396751 | A | G | 172 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(169): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.97-18628T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396751 | |||||||
| chr2:39396848 | T | TCA | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.97-18727_97-18726d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396848 | |||||||
| chr2:39396915 | T | A | 7 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0035 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-18792A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396915 | |||||||
| chr2:39396994 | T | A | 2 | a0001c0003t0012g0004 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.97-18871A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39396994 | |||||||
| chr2:39397302 | G | A | 167 | a0001c0001t0001g0180 a0001c0001t0002g0030 a0001c0001t0002g0031 others(164): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.97-19179C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39397302 | |||||||
| chr2:39397363 | G | C | 20 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(17): Show |
20 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.97-19240C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39397363 | |||||||
| chr2:39397498 | A | G | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.97-19375T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39397498 | |||||||
| chr2:39397499 | A | G | 1 | a0001c0002t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.97-19376T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39397499 | |||||||
| chr2:39397626 | C | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-19503G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39397626 | |||||||
| chr2:39397775 | T | C | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97-19652A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39397775 | |||||||
| chr2:39397785 | G | A | 3 | a0001c0002t0010g0210 a0001c0002t0010g0211 a0001c0002t0010g0213 |
3 | HG02165.hp2 HG03834.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.97-19662C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39397785 | |||||||
| chr2:39397799 | A | T | 136 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(133): Show |
136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.97-19676T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39397799 | |||||||
| chr2:39397872 | C | T | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97-19749G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39397872 | |||||||
| chr2:39398081 | C | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-19958G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398081 | |||||||
| chr2:39398148 | C | T | 1 | a0001c0002t0001g0085 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.97-20025G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398148 | |||||||
| chr2:39398532 | G | A | 1 | a0001c0003t0004g0229 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.97-20409C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398532 | |||||||
| chr2:39398590 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-20467A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398590 | |||||||
| chr2:39398713 | A | AAAT | 12 | a0001c0001t0002g0104 a0001c0001t0002g0108 a0001c0002t0001g0046 others(9): Show |
12 | HG00140.hp1 HG01358.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.97-20593_97-20591d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398713 | |||||||
| chr2:39398713 | A | AAATAAT | 35 | a0001c0001t0002g0018 a0001c0001t0002g0045 a0001c0001t0002g0106 others(32): Show |
35 | HG00408.hp1 HG00738.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.97-20596_97-20591d others(8): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398713 | |||||||
| chr2:39398713 | A | AAATAATA others(2): Show |
36 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(33): Show |
36 | HG00609.hp1 HG01081.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.97-20599_97-20591d others(11): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398713 | |||||||
| chr2:39398713 | A | AAATAATA others(5): Show |
7 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0117 others(4): Show |
7 | HG00741.hp1 HG01496.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-20602_97-20591d others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398713 | |||||||
| chr2:39398713 | A | AAATAATA others(8): Show |
1 | a0001c0001t0002g0140 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.97-20605_97-20591d others(17): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398713 | |||||||
| chr2:39398713 | A | AAATAATA others(11): Show |
2 | a0001c0001t0002g0141 a0001c0003t0012g0004 |
2 | HG02886.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.97-20608_97-20591d others(20): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398713 | |||||||
| chr2:39398735 | AATAATAA others(5): Show |
A | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.97-20624_97-20613d others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398735 | |||||||
| chr2:39398738 | A | G | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-20615T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398738 | |||||||
| chr2:39398738 | AATAATAA others(2): Show |
A | 22 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(19): Show |
22 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.97-20624_97-20616d others(11): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398738 | |||||||
| chr2:39398741 | A | G | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-20618T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398741 | |||||||
| chr2:39398744 | A | AATAATAA others(8): Show |
1 | a0001c0001t0002g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.97-20622_97-20621i others(17): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398744 | |||||||
| chr2:39398744 | AATG | A | 24 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(21): Show |
24 | HG01099.hp2 HG01243.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.97-20624_97-20622d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398744 | |||||||
| chr2:39398744 | AATGATGA others(4): Show |
A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-20632_97-20622d others(13): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398744 | |||||||
| chr2:39398747 | G | A | 113 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(110): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.97-20624C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398747 | |||||||
| chr2:39398902 | G | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-20779C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39398902 | |||||||
| chr2:39399044 | T | TA | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.97-20922dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39399044 | |||||||
| chr2:39399044 | TA | T | 17 | a0001c0001t0002g0029 a0001c0001t0002g0097 a0001c0001t0002g0098 others(14): Show |
17 | HG00140.hp2 HG01257.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.97-20922delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39399044 | |||||||
| chr2:39399247 | A | G | 116 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(113): Show |
116 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.97-21124T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39399247 | |||||||
| chr2:39399286 | G | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-21163C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39399286 | |||||||
| chr2:39399406 | A | G | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0035 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-21283T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39399406 | |||||||
| chr2:39399496 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-21373G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39399496 | |||||||
| chr2:39399797 | C | T | 1 | a0001c0002t0001g0037 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.97-21674G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39399797 | |||||||
| chr2:39399999 | A | T | 3 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 |
3 | HG01109.hp2 HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.97-21876T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39399999 | |||||||
| chr2:39400006 | A | G | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-21883T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39400006 | |||||||
| chr2:39400269 | C | G | 1 | a0001c0001t0002g0140 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.97-22146G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39400269 | |||||||
| chr2:39400314 | T | A | 171 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.97-22191A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39400314 | |||||||
| chr2:39400401 | G | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-22278C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39400401 | |||||||
| chr2:39400733 | A | G | 2 | a0001c0003t0004g0225 a0001c0003t0004g0226 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.97-22610T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39400733 | |||||||
| chr2:39400770 | A | G | 15 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(12): Show |
15 | HG00408.hp1 HG01934.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.97-22647T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39400770 | |||||||
| chr2:39400812 | A | C | 226 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(223): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.97-22689T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39400812 | |||||||
| chr2:39401080 | G | A | 2 | a0001c0002t0001g0039 a0001c0002t0001g0085 |
2 | NA18981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.97-22957C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39401080 | |||||||
| chr2:39401100 | T | C | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.97-22977A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39401100 | |||||||
| chr2:39401104 | G | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-22981C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39401104 | |||||||
| chr2:39401446 | T | A | 18 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(15): Show |
18 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.97-23323A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39401446 | |||||||
| chr2:39401662 | A | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.97-23539T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39401662 | |||||||
| chr2:39401730 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.97-23607C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39401730 | |||||||
| chr2:39401930 | T | C | 1 | a0001c0001t0002g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.97-23807A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39401930 | |||||||
| chr2:39402230 | T | C | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.97-24107A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39402230 | |||||||
| chr2:39402330 | AT | A | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.97-24208delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39402330 | |||||||
| chr2:39402527 | C | T | 1 | a0001c0003t0004g0222 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.97-24404G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39402527 | |||||||
| chr2:39402611 | G | A | 1 | a0001c0002t0001g0132 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.97-24488C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39402611 | |||||||
| chr2:39402764 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-24641G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39402764 | |||||||
| chr2:39402869 | A | G | 3 | a0001c0003t0004g0215 a0001c0003t0004g0225 a0001c0003t0004g0226 |
3 | HG03490.hp2 HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.97-24746T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39402869 | |||||||
| chr2:39402970 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-24847A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39402970 | |||||||
| chr2:39403180 | G | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-25057C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39403180 | |||||||
| chr2:39403195 | C | T | 1 | a0001c0002t0001g0037 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.97-25072G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39403195 | |||||||
| chr2:39403250 | T | C | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.97-25127A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39403250 | |||||||
| chr2:39403254 | C | A | 1 | a0001c0002t0001g0127 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.97-25131G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39403254 | |||||||
| chr2:39403406 | T | C | 1 | a0001c0001t0003g0177 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.97-25283A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39403406 | |||||||
| chr2:39403449 | A | G | 59 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(56): Show |
59 | HG00280.hp2 HG00609.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.97-25326T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39403449 | |||||||
| chr2:39403470 | T | C | 3 | a0001c0003t0004g0216 a0001c0003t0004g0231 a0001c0003t0004g0232 |
3 | HG02129.hp2 HG02132.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.97-25347A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39403470 | |||||||
| chr2:39403499 | A | G | 1 | a0001c0002t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.97-25376T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39403499 | |||||||
| chr2:39403500 | T | A | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.97-25377A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39403500 | |||||||
| chr2:39403516 | C | G | 64 | a0001c0001t0002g0056 a0001c0002t0001g0026 a0001c0002t0001g0037 others(61): Show |
64 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.97-25393G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39403516 | |||||||
| chr2:39403629 | A | T | 1 | a0001c0002t0001g0063 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.97-25506T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39403629 | |||||||
| chr2:39403785 | C | G | 1 | a0001c0002t0001g0046 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.97-25662G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39403785 | |||||||
| chr2:39403945 | G | C | 1 | a0001c0002t0001g0127 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.97-25822C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39403945 | |||||||
| chr2:39404351 | C | T | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0035 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-26228G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39404351 | |||||||
| chr2:39404531 | C | T | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.97-26408G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39404531 | |||||||
| chr2:39404609 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-26486G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39404609 | |||||||
| chr2:39404617 | C | CT | 11 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0172 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-26495dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39404617 | |||||||
| chr2:39404617 | CT | C | 104 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(101): Show |
104 | HG00280.hp2 HG00609.hp1 HG00741.hp1 others(101): Show |
intron_variant | MODIFIER | c.97-26495delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39404617 | |||||||
| chr2:39404622 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.97-26499A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39404622 | |||||||
| chr2:39404666 | G | C | 1 | a0001c0001t0002g0045 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.97-26543C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39404666 | |||||||
| chr2:39404680 | G | A | 1 | a0001c0002t0001g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.97-26557C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39404680 | |||||||
| chr2:39404811 | G | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-26688C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39404811 | |||||||
| chr2:39404863 | C | T | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-26740G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39404863 | |||||||
| chr2:39405004 | T | C | 7 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0035 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-26881A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405004 | |||||||
| chr2:39405027 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-26904A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405027 | |||||||
| chr2:39405054 | T | C | 5 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(2): Show |
5 | HG01099.hp2 HG02257.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-26931A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405054 | |||||||
| chr2:39405091 | T | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-26968A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405091 | |||||||
| chr2:39405173 | A | C | 211 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(208): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.97-27050T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405173 | |||||||
| chr2:39405197 | C | T | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97-27074G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405197 | |||||||
| chr2:39405225 | G | C | 6 | a0001c0002t0001g0037 a0001c0002t0001g0080 a0001c0002t0001g0134 others(3): Show |
6 | NA18942.hp2 NA18986.hp2 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-27102C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405225 | |||||||
| chr2:39405226 | A | G | 1 | a0001c0001t0005g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.97-27103T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405226 | |||||||
| chr2:39405229 | G | A | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-27106C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405229 | |||||||
| chr2:39405234 | G | A | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.97-27111C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405234 | |||||||
| chr2:39405274 | C | A | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.97-27151G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405274 | |||||||
| chr2:39405279 | T | G | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-27156A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405279 | |||||||
| chr2:39405289 | G | A | 18 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(15): Show |
18 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.97-27166C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405289 | |||||||
| chr2:39405294 | T | G | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.97-27171A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405294 | |||||||
| chr2:39405397 | G | C | 1 | a0001c0001t0002g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.97-27274C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405397 | |||||||
| chr2:39405472 | G | T | 1 | a0001c0001t0005g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.97-27349C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405472 | |||||||
| chr2:39405521 | C | T | 2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.97-27398G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405521 | |||||||
| chr2:39405557 | C | T | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97-27434G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405557 | |||||||
| chr2:39405627 | A | G | 211 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(208): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.97-27504T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405627 | |||||||
| chr2:39405740 | C | T | 1 | a0001c0001t0006g0199 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.97-27617G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405740 | |||||||
| chr2:39405998 | G | C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.97-27875C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39405998 | |||||||
| chr2:39406173 | C | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-28050G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39406173 | |||||||
| chr2:39406627 | A | G | 1 | a0001c0004t0013g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.97-28504T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39406627 | |||||||
| chr2:39406790 | T | C | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.97-28667A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39406790 | |||||||
| chr2:39406878 | A | C | 1 | a0001c0001t0003g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.97-28755T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39406878 | |||||||
| chr2:39407053 | A | G | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.97-28930T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39407053 | |||||||
| chr2:39407141 | A | G | 1 | a0001c0002t0001g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.97-29018T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39407141 | |||||||
| chr2:39407175 | CCTGATAC others(16): Show |
C | 2 | a0001c0002t0009g0129 a0001c0008t0002g0088 |
2 | NA19012.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.97-29075_97-29053d others(25): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39407175 | |||||||
| chr2:39407195 | C | G | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.97-29072G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39407195 | |||||||
| chr2:39407303 | G | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-29180C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39407303 | |||||||
| chr2:39407419 | G | A | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97-29296C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39407419 | |||||||
| chr2:39407436 | C | T | 1 | a0001c0002t0001g0037 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.97-29313G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39407436 | |||||||
| chr2:39407455 | A | G | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.97-29332T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39407455 | |||||||
| chr2:39407615 | A | G | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.96+29277T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39407615 | |||||||
| chr2:39408127 | C | A | 1 | a0001c0004t0013g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.96+28765G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39408127 | |||||||
| chr2:39408153 | T | C | 1 | a0001c0002t0001g0193 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.96+28739A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39408153 | |||||||
| chr2:39408162 | C | T | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+28730G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39408162 | |||||||
| chr2:39408505 | G | GA | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0130 |
3 | NA18948.hp1 NA18960.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.96+28386dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39408505 | |||||||
| chr2:39408561 | A | C | 2 | a0001c0003t0004g0225 a0001c0003t0004g0226 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.96+28331T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39408561 | |||||||
| chr2:39408621 | A | C | 19 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 others(16): Show |
19 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.96+28271T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39408621 | |||||||
| chr2:39408639 | C | CA | 203 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(200): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.96+28252dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39408639 | |||||||
| chr2:39408639 | C | CAA | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0006g0205 others(3): Show |
6 | HG02257.hp1 HG02486.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+28251_96+28252d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39408639 | |||||||
| chr2:39408690 | T | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.96+28202A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39408690 | |||||||
| chr2:39408766 | G | C | 21 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 others(18): Show |
21 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+28126C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39408766 | |||||||
| chr2:39408843 | A | C | 1 | a0001c0002t0001g0037 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.96+28049T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39408843 | |||||||
| chr2:39408856 | G | C | 1 | a0001c0002t0001g0026 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.96+28036C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39408856 | |||||||
| chr2:39408913 | C | A | 1 | a0001c0001t0002g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.96+27979G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39408913 | |||||||
| chr2:39409271 | A | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+27621T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39409271 | |||||||
| chr2:39409281 | T | A | 23 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(20): Show |
23 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.96+27611A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39409281 | |||||||
| chr2:39409328 | G | A | 23 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(20): Show |
23 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.96+27564C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39409328 | |||||||
| chr2:39409366 | G | C | 21 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(18): Show |
21 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.96+27526C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39409366 | |||||||
| chr2:39409411 | T | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+27481A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39409411 | |||||||
| chr2:39409456 | C | T | 3 | a0001c0001t0002g0106 a0001c0001t0002g0140 a0001c0001t0002g0141 |
3 | NA18945.hp1 NA18946.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.96+27436G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39409456 | |||||||
| chr2:39409587 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+27305G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39409587 | |||||||
| chr2:39409634 | T | C | 3 | a0001c0002t0001g0131 a0001c0002t0001g0132 a0001c0002t0001g0151 |
3 | HG03831.hp1 HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.96+27258A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39409634 | |||||||
| chr2:39409695 | G | T | 2 | a0001c0005t0002g0033 a0001c0005t0002g0034 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.96+27197C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39409695 | |||||||
| chr2:39409776 | A | G | 1 | a0001c0002t0001g0144 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.96+27116T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39409776 | |||||||
| chr2:39409911 | T | C | 7 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0035 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+26981A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39409911 | |||||||
| chr2:39410181 | C | T | 1 | a0001c0002t0001g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.96+26711G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39410181 | |||||||
| chr2:39410187 | T | C | 23 | a0001c0001t0001g0180 a0001c0001t0003g0032 a0001c0001t0003g0173 others(20): Show |
23 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.96+26705A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39410187 | |||||||
| chr2:39410543 | T | C | 1 | a0001c0002t0001g0089 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.96+26349A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39410543 | |||||||
| chr2:39410558 | T | C | 4 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(1): Show |
4 | HG01496.hp1 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+26334A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39410558 | |||||||
| chr2:39410774 | T | C | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.96+26118A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39410774 | |||||||
| chr2:39410823 | G | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+26069C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39410823 | |||||||
| chr2:39410891 | T | C | 1 | a0001c0002t0001g0127 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.96+26001A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39410891 | |||||||
| chr2:39410955 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+25937G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39410955 | |||||||
| chr2:39411537 | T | G | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.96+25355A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39411537 | |||||||
| chr2:39411606 | A | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.96+25286T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39411606 | |||||||
| chr2:39411690 | T | TA | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+25201dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39411690 | |||||||
| chr2:39411891 | T | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+25001A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39411891 | |||||||
| chr2:39411900 | G | A | 3 | a0001c0001t0002g0106 a0001c0001t0002g0140 a0001c0001t0002g0141 |
3 | NA18945.hp1 NA18946.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.96+24992C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39411900 | |||||||
| chr2:39411918 | G | A | 1 | a0001c0004t0013g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.96+24974C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39411918 | |||||||
| chr2:39412234 | C | T | 3 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 |
3 | HG00280.hp1 HG00738.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.96+24658G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39412234 | |||||||
| chr2:39412258 | C | T | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.96+24634G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39412258 | |||||||
| chr2:39412285 | T | C | 9 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0002t0001g0146 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+24607A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39412285 | |||||||
| chr2:39412338 | C | T | 12 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+24554G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39412338 | |||||||
| chr2:39412395 | T | C | 1 | a0001c0002t0001g0083 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.96+24497A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39412395 | |||||||
| chr2:39412431 | C | T | 118 | a0001c0001t0001g0180 a0001c0001t0002g0052 a0001c0001t0002g0053 others(115): Show |
118 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.96+24461G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39412431 | |||||||
| chr2:39412537 | CT | C | 181 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.96+24354delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39412537 | |||||||
| chr2:39413075 | A | G | 19 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 others(16): Show |
19 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.96+23817T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413075 | |||||||
| chr2:39413081 | T | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+23811A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413081 | |||||||
| chr2:39413124 | T | C | 9 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0035 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+23768A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413124 | |||||||
| chr2:39413337 | G | A | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.96+23555C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413337 | |||||||
| chr2:39413352 | A | G | 9 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0035 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+23540T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413352 | |||||||
| chr2:39413423 | G | GT | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.96+23468dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413423 | |||||||
| chr2:39413456 | T | C | 1 | a0001c0002t0001g0084 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.96+23436A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413456 | |||||||
| chr2:39413578 | T | C | 1 | a0001c0001t0002g0107 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.96+23314A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413578 | |||||||
| chr2:39413587 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.96+23305T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413587 | |||||||
| chr2:39413598 | A | C | 174 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(171): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.96+23294T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413598 | |||||||
| chr2:39413626 | C | G | 2 | a0001c0002t0001g0060 a0001c0002t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.96+23266G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413626 | |||||||
| chr2:39413675 | A | G | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.96+23217T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413675 | |||||||
| chr2:39413705 | ACCAGACA others(7): Show |
A | 19 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 others(16): Show |
19 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.96+23173_96+23186d others(16): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413705 | |||||||
| chr2:39413738 | T | C | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.96+23154A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413738 | |||||||
| chr2:39413752 | A | G | 157 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.96+23140T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413752 | |||||||
| chr2:39413824 | T | A | 1 | a0001c0001t0002g0053 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.96+23068A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413824 | |||||||
| chr2:39413885 | G | A | 3 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 |
3 | HG00280.hp1 HG00738.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.96+23007C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413885 | |||||||
| chr2:39413942 | T | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.96+22950A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39413942 | |||||||
| chr2:39414179 | C | T | 1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.96+22713G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39414179 | |||||||
| chr2:39414284 | A | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+22608T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39414284 | |||||||
| chr2:39414404 | C | A | 2 | a0001c0002t0001g0039 a0001c0002t0001g0085 |
2 | NA18981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.96+22488G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39414404 | |||||||
| chr2:39414415 | C | T | 173 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(170): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.96+22477G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39414415 | |||||||
| chr2:39414604 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.96+22288C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39414604 | |||||||
| chr2:39414678 | A | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+22214T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39414678 | |||||||
| chr2:39414703 | G | A | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.96+22189C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39414703 | |||||||
| chr2:39415377 | CAAGT | C | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0035 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+21511_96+21514d others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415377 | |||||||
| chr2:39415525 | ATTAC | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+21363_96+21366d others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415525 | |||||||
| chr2:39415573 | G | A | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.96+21319C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415573 | |||||||
| chr2:39415679 | C | T | 1 | a0003c0009t0005g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.96+21213G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415679 | |||||||
| chr2:39415890 | T | G | 1 | a0001c0001t0002g0209 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.96+21002A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415890 | |||||||
| chr2:39415976 | A | AATATATA others(5): Show |
1 | a0001c0003t0004g0227 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.96+20915_96+20916i others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415976 | |||||||
| chr2:39415978 | A | AATATATA others(9): Show |
1 | a0001c0002t0001g0144 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.96+20913_96+20914i others(18): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415978 | |||||||
| chr2:39415978 | A | AATATATA others(11): Show |
1 | a0001c0001t0003g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.96+20913_96+20914i others(20): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415978 | |||||||
| chr2:39415978 | A | AATATATA others(19): Show |
1 | a0001c0001t0002g0027 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.96+20913_96+20914i others(28): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415978 | |||||||
| chr2:39415978 | A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.96+20913_96+20914i others(21): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415978 | |||||||
| chr2:39415978 | A | T | 1 | a0001c0003t0004g0227 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.96+20914T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415978 | |||||||
| chr2:39415980 | A | AAAAAAAA others(37): Show |
1 | a0001c0008t0002g0088 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(46): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(20): Show |
1 | a0001c0002t0009g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(29): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(31): Show |
1 | a0001c0002t0009g0129 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(40): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(12): Show |
1 | a0001c0002t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(21): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(9): Show |
1 | a0001c0002t0001g0069 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(18): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(20): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(13): Show |
2 | a0001c0002t0001g0094 a0001c0002t0001g0196 |
2 | NA18954.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(22): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(15): Show |
1 | a0001c0002t0001g0076 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(24): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(23): Show |
1 | a0001c0001t0003g0174 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(32): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(8): Show |
1 | a0001c0002t0001g0089 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(17): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(10): Show |
1 | a0001c0002t0001g0083 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(19): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(12): Show |
3 | a0001c0001t0003g0191 a0001c0001t0003g0194 a0001c0002t0001g0057 |
3 | HG00408.hp2 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(21): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(16): Show |
1 | a0001c0002t0001g0134 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(25): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(18): Show |
1 | a0001c0002t0001g0195 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(27): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(7): Show |
1 | a0001c0002t0001g0120 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(16): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(11): Show |
3 | a0001c0002t0001g0081 a0001c0002t0001g0132 a0001c0002t0010g0211 |
3 | HG04115.hp1 NA18948.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(20): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(21): Show |
1 | a0001c0003t0004g0219 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(30): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(27): Show |
1 | a0001c0002t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(36): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(4): Show |
1 | a0001c0002t0001g0124 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(13): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(6): Show |
6 | a0001c0001t0002g0056 a0001c0002t0001g0040 a0001c0002t0001g0063 others(3): Show |
6 | HG01106.hp1 HG02129.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+20911_96+20912i others(15): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(8): Show |
6 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0055 others(3): Show |
6 | NA18946.hp2 NA18973.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+20911_96+20912i others(17): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(10): Show |
3 | a0001c0001t0002g0143 a0001c0001t0003g0173 a0001c0002t0010g0210 |
3 | HG03834.hp2 HG04199.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(19): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(12): Show |
5 | a0001c0001t0003g0179 a0001c0001t0003g0182 a0001c0001t0003g0185 others(2): Show |
5 | HG02165.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+20911_96+20912i others(21): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(14): Show |
2 | a0001c0002t0001g0044 a0001c0003t0004g0222 |
2 | HG01167.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(23): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(16): Show |
1 | a0001c0002t0001g0043 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(25): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(18): Show |
2 | a0001c0001t0003g0183 a0001c0002t0001g0096 |
2 | HG01109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(27): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(22): Show |
1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(31): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(28): Show |
1 | a0001c0002t0001g0115 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(37): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(3): Show |
1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(12): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(5): Show |
3 | a0001c0001t0008g0049 a0001c0001t0008g0051 a0001c0002t0001g0073 |
3 | HG00280.hp1 HG01081.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(7): Show |
3 | a0001c0001t0002g0054 a0001c0002t0001g0075 a0001c0002t0001g0080 |
3 | HG03710.hp2 HG03831.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(16): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(11): Show |
5 | a0001c0001t0003g0186 a0001c0001t0003g0206 a0001c0002t0001g0059 others(2): Show |
5 | HG02055.hp2 HG02132.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+20911_96+20912i others(20): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(13): Show |
2 | a0001c0002t0001g0082 a0001c0002t0001g0130 |
2 | NA18960.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(22): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0003g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(24): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(21): Show |
1 | a0001c0002t0001g0047 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(30): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(25): Show |
2 | a0001c0002t0001g0046 a0001c0002t0001g0148 |
2 | HG00741.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(34): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(29): Show |
1 | a0001c0002t0001g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(38): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAA others(33): Show |
2 | a0001c0002t0001g0095 a0001c0002t0001g0113 |
2 | HG00280.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(42): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAT others(4): Show |
3 | a0001c0002t0001g0066 a0001c0002t0001g0079 a0001c0002t0001g0092 |
3 | HG03041.hp1 NA18952.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(13): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAT others(6): Show |
6 | a0001c0002t0001g0026 a0001c0002t0001g0060 a0001c0002t0001g0061 others(3): Show |
6 | HG01168.hp2 HG01169.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+20911_96+20912i others(15): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAT others(8): Show |
7 | a0001c0002t0001g0039 a0001c0002t0001g0058 a0001c0002t0001g0062 others(4): Show |
7 | HG01099.hp1 HG01952.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+20911_96+20912i others(17): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAT others(12): Show |
1 | a0001c0001t0003g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(21): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAT others(18): Show |
1 | a0004c0006t0004g0220 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(27): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAT others(20): Show |
1 | a0001c0001t0003g0175 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(29): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAAAT others(24): Show |
1 | a0001c0002t0001g0146 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(33): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAATA others(5): Show |
2 | a0001c0002t0001g0064 a0001c0002t0001g0151 |
2 | HG01928.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAATA others(7): Show |
2 | a0001c0001t0005g0007 a0001c0002t0001g0072 |
2 | HG00609.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(16): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAATA others(9): Show |
1 | a0001c0002t0001g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(18): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAATA others(13): Show |
3 | a0001c0002t0001g0112 a0001c0003t0004g0214 a0001c0003t0007g0221 |
3 | HG03017.hp2 NA18954.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(22): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAATA others(17): Show |
2 | a0001c0001t0003g0178 a0001c0003t0004g0218 |
2 | HG00408.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(26): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAATA others(19): Show |
1 | a0001c0001t0003g0181 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(28): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAATA others(21): Show |
4 | a0001c0001t0003g0176 a0001c0003t0004g0215 a0001c0003t0004g0225 others(1): Show |
4 | HG01099.hp2 HG03492.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+20911_96+20912i others(30): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAATA others(27): Show |
1 | a0001c0002t0001g0147 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(36): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAAATA others(29): Show |
2 | a0001c0001t0002g0035 a0001c0002t0001g0145 |
2 | HG01168.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(38): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAATAT others(4): Show |
3 | a0001c0001t0002g0030 a0001c0001t0014g0189 a0001c0004t0005g0002 |
3 | HG02895.hp1 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(13): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAATAT others(6): Show |
4 | a0001c0001t0008g0050 a0001c0002t0001g0038 a0001c0002t0001g0068 others(1): Show |
4 | HG00738.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+20911_96+20912i others(15): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAATAT others(10): Show |
1 | a0001c0002t0001g0037 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(19): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAATAT others(16): Show |
1 | a0001c0001t0003g0177 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(25): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAATAT others(20): Show |
1 | a0001c0003t0004g0226 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(29): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAATAT others(22): Show |
2 | a0001c0003t0004g0217 a0001c0003t0004g0229 |
2 | NA18953.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(31): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAAATAT others(26): Show |
1 | a0001c0002t0001g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(35): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAATATA others(3): Show |
1 | a0001c0002t0001g0074 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.96+20911_96+20912i others(12): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAATATA others(5): Show |
1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(14): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAATATA others(7): Show |
2 | a0001c0002t0001g0142 a0001c0002t0009g0041 |
2 | HG02602.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(16): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAAATATA others(29): Show |
1 | a0001c0001t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(38): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAATATAT others(6): Show |
1 | a0001c0002t0001g0138 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(15): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAATATAT others(10): Show |
1 | a0001c0003t0004g0231 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(19): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAATATAT others(14): Show |
2 | a0001c0001t0002g0029 a0001c0003t0004g0232 |
2 | HG01496.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(23): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAATATAT others(22): Show |
1 | a0001c0002t0001g0207 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(31): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AAATATAT others(24): Show |
1 | a0001c0002t0001g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.96+20911_96+20912i others(33): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AATATATA others(7): Show |
1 | a0001c0001t0002g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.96+20898_96+20911d others(16): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AATATATA others(9): Show |
1 | a0001c0003t0004g0216 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.96+20896_96+20911d others(18): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AATATATA others(15): Show |
1 | a0001c0001t0003g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.96+20890_96+20911d others(24): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | AT | 3 | a0001c0001t0002g0024 a0001c0001t0002g0116 a0001c0001t0002g0158 |
3 | HG02165.hp1 HG02886.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.96+20911_96+20912i others(3): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | ATAT | 7 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(4): Show |
7 | HG03139.hp2 NA18953.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+20911_96+20912i others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | A | T | 5 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0003g0188 others(2): Show |
5 | HG00140.hp1 HG01243.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+20912T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415980 | AAT | A | 7 | a0001c0001t0002g0104 a0001c0001t0002g0152 a0001c0001t0002g0156 others(4): Show |
7 | HG00738.hp2 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+20910_96+20911d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415980 | |||||||
| chr2:39415981 | AT | A | 12 | a0001c0001t0002g0045 a0001c0001t0002g0099 a0001c0001t0002g0107 others(9): Show |
12 | HG01255.hp1 HG01496.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+20910delA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415981 | |||||||
| chr2:39415982 | T | A | 16 | a0001c0001t0002g0025 a0001c0001t0002g0097 a0001c0001t0002g0105 others(13): Show |
16 | HG01106.hp2 HG01243.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.96+20910A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415982 | |||||||
| chr2:39415984 | T | A | 3 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0005t0002g0034 |
3 | HG01243.hp1 HG01255.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.96+20908A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415984 | |||||||
| chr2:39415996 | TATATATA others(3): Show |
T | 3 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 |
3 | HG01109.hp2 HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.96+20886_96+20895d others(12): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39415996 | |||||||
| chr2:39416002 | T | A | 2 | a0001c0001t0002g0035 a0001c0002t0001g0126 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.96+20890A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39416002 | |||||||
| chr2:39416002 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+20890A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39416002 | |||||||
| chr2:39416002 | TATAAAA | T | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.96+20884_96+20889d others(8): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39416002 | |||||||
| chr2:39416004 | T | A | 3 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0148 |
3 | HG00741.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.96+20888A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39416004 | |||||||
| chr2:39416006 | A | T | 65 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(62): Show |
65 | HG00140.hp1 HG00408.hp1 HG01099.hp2 others(62): Show |
intron_variant | MODIFIER | c.96+20886T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39416006 | |||||||
| chr2:39416008 | A | T | 16 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(13): Show |
16 | HG01496.hp1 HG02258.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.96+20884T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39416008 | |||||||
| chr2:39416307 | A | C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.96+20585T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39416307 | |||||||
| chr2:39416436 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.96+20456C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39416436 | |||||||
| chr2:39416485 | T | A | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.96+20407A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39416485 | |||||||
| chr2:39416993 | C | T | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.96+19899G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39416993 | |||||||
| chr2:39417215 | C | CT | 44 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0139 others(41): Show |
44 | HG00140.hp1 HG00408.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.96+19676dupA | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39417215 | |||||||
| chr2:39417312 | C | T | 134 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(131): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.96+19580G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39417312 | |||||||
| chr2:39417369 | G | A | 96 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(93): Show |
96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.96+19523C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39417369 | |||||||
| chr2:39417378 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+19514G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39417378 | |||||||
| chr2:39417464 | C | A | 1 | a0001c0001t0002g0025 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.96+19428G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39417464 | |||||||
| chr2:39417470 | C | T | 37 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(34): Show |
37 | HG00609.hp1 HG00741.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.96+19422G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39417470 | |||||||
| chr2:39417507 | C | T | 3 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0055 |
3 | NA18998.hp2 NA19012.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.96+19385G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39417507 | |||||||
| chr2:39417641 | C | T | 4 | a0001c0002t0001g0095 a0001c0002t0001g0096 a0001c0002t0001g0113 others(1): Show |
4 | HG00280.hp2 HG01109.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+19251G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39417641 | |||||||
| chr2:39417679 | C | T | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.96+19213G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39417679 | |||||||
| chr2:39417736 | G | C | 6 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(3): Show |
6 | HG03831.hp2 NA18998.hp2 NA19012.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+19156C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39417736 | |||||||
| chr2:39417765 | C | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+19127G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39417765 | |||||||
| chr2:39417781 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+19111A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39417781 | |||||||
| chr2:39417942 | C | A | 1 | a0001c0002t0001g0113 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.96+18950G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39417942 | |||||||
| chr2:39418026 | C | T | 1 | a0001c0001t0006g0198 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.96+18866G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39418026 | |||||||
| chr2:39418063 | T | C | 200 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(197): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.96+18829A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39418063 | |||||||
| chr2:39418089 | C | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+18803G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39418089 | |||||||
| chr2:39418198 | G | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.96+18694C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39418198 | |||||||
| chr2:39418202 | CA | C | 201 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(198): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.96+18689delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39418202 | |||||||
| chr2:39418281 | G | A | 1 | a0001c0002t0001g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.96+18611C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39418281 | |||||||
| chr2:39418292 | C | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+18600G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39418292 | |||||||
| chr2:39418294 | G | C | 1 | a0001c0003t0002g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.96+18598C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39418294 | |||||||
| chr2:39418457 | C | G | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+18435G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39418457 | |||||||
| chr2:39418514 | T | C | 31 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(28): Show |
31 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.96+18378A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39418514 | |||||||
| chr2:39418522 | A | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.96+18370T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39418522 | |||||||
| chr2:39418641 | T | C | 12 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+18251A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39418641 | |||||||
| chr2:39418769 | C | T | 7 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+18123G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39418769 | |||||||
| chr2:39419113 | G | A | 1 | a0001c0008t0002g0088 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.96+17779C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39419113 | |||||||
| chr2:39419202 | T | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.96+17690A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39419202 | |||||||
| chr2:39419231 | A | C | 1 | a0001c0001t0003g0206 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.96+17661T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39419231 | |||||||
| chr2:39419932 | A | T | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+16960T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39419932 | |||||||
| chr2:39420059 | A | T | 33 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(30): Show |
33 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.96+16833T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39420059 | |||||||
| chr2:39420080 | T | C | 75 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(72): Show |
75 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.96+16812A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39420080 | |||||||
| chr2:39420330 | T | C | 3 | a0001c0001t0003g0188 a0001c0001t0003g0190 a0001c0001t0014g0189 |
3 | HG01243.hp2 HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.96+16562A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39420330 | |||||||
| chr2:39420425 | G | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+16467C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39420425 | |||||||
| chr2:39420469 | T | G | 6 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(3): Show |
6 | HG01496.hp1 HG02717.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+16423A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39420469 | |||||||
| chr2:39420529 | G | A | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+16363C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39420529 | |||||||
| chr2:39420575 | C | G | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.96+16317G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39420575 | |||||||
| chr2:39420954 | T | C | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.96+15938A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39420954 | |||||||
| chr2:39421261 | T | C | 1 | a0001c0001t0002g0116 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.96+15631A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39421261 | |||||||
| chr2:39421368 | ATT | A | 39 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0027 others(36): Show |
39 | HG00408.hp2 HG00741.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.96+15522_96+15523d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39421368 | |||||||
| chr2:39421368 | ATTT | A | 155 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(152): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.96+15521_96+15523d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39421368 | |||||||
| chr2:39421368 | ATTTT | A | 16 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0005g0007 others(13): Show |
16 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.96+15520_96+15523d others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39421368 | |||||||
| chr2:39421556 | T | A | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+15336A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39421556 | |||||||
| chr2:39421585 | G | A | 1 | a0001c0002t0001g0089 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.96+15307C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39421585 | |||||||
| chr2:39421621 | T | A | 19 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 others(16): Show |
19 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.96+15271A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39421621 | |||||||
| chr2:39421684 | G | A | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+15208C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39421684 | |||||||
| chr2:39421738 | T | C | 1 | a0001c0002t0001g0037 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.96+15154A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39421738 | |||||||
| chr2:39421809 | T | A | 21 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 others(18): Show |
21 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+15083A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39421809 | |||||||
| chr2:39421927 | C | A | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.96+14965G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39421927 | |||||||
| chr2:39421969 | T | C | 135 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(132): Show |
135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.96+14923A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39421969 | |||||||
| chr2:39422241 | T | G | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+14651A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39422241 | |||||||
| chr2:39422249 | T | C | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+14643A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39422249 | |||||||
| chr2:39422320 | C | T | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.96+14572G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39422320 | |||||||
| chr2:39422513 | T | C | 200 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(197): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.96+14379A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39422513 | |||||||
| chr2:39422528 | C | T | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+14364G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39422528 | |||||||
| chr2:39422574 | T | A | 1 | a0001c0001t0016g0212 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.96+14318A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39422574 | |||||||
| chr2:39422649 | T | C | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.96+14243A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39422649 | |||||||
| chr2:39422668 | C | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.96+14224G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39422668 | |||||||
| chr2:39422712 | G | A | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+14180C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39422712 | |||||||
| chr2:39422733 | T | C | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+14159A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39422733 | |||||||
| chr2:39422924 | A | T | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+13968T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39422924 | |||||||
| chr2:39422992 | G | A | 3 | a0001c0003t0004g0216 a0001c0003t0004g0231 a0001c0003t0004g0232 |
3 | HG02129.hp2 HG02132.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.96+13900C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39422992 | |||||||
| chr2:39423318 | G | A | 1 | a0001c0001t0002g0209 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.96+13574C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39423318 | |||||||
| chr2:39423771 | T | C | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.96+13121A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39423771 | |||||||
| chr2:39423966 | C | T | 1 | a0001c0001t0003g0175 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.96+12926G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39423966 | |||||||
| chr2:39424065 | T | A | 1 | a0001c0001t0002g0025 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.96+12827A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424065 | |||||||
| chr2:39424191 | G | T | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+12701C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424191 | |||||||
| chr2:39424239 | C | T | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+12653G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424239 | |||||||
| chr2:39424337 | T | C | 12 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+12555A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424337 | |||||||
| chr2:39424455 | G | A | 1 | a0001c0002t0001g0148 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.96+12437C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424455 | |||||||
| chr2:39424467 | G | C | 1 | a0001c0003t0004g0214 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.96+12425C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424467 | |||||||
| chr2:39424690 | C | G | 2 | a0001c0001t0015g0192 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.96+12202G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424690 | |||||||
| chr2:39424695 | T | C | 58 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(55): Show |
58 | HG00280.hp2 HG00609.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.96+12197A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424695 | |||||||
| chr2:39424830 | C | CA | 22 | a0001c0001t0001g0180 a0001c0001t0002g0117 a0001c0001t0002g0118 others(19): Show |
22 | HG00741.hp1 HG01243.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+12061dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424830 | |||||||
| chr2:39424830 | C | CAA | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.96+12060_96+12061d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424830 | |||||||
| chr2:39424830 | C | CAAA | 16 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(13): Show |
16 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.96+12059_96+12061d others(5): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424830 | |||||||
| chr2:39424830 | C | CAAAA | 14 | a0001c0002t0007g0230 a0001c0003t0004g0214 a0001c0003t0004g0215 others(11): Show |
14 | HG00140.hp1 HG01934.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.96+12058_96+12061d others(6): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424830 | |||||||
| chr2:39424830 | CA | C | 74 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(71): Show |
74 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.96+12061delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424830 | |||||||
| chr2:39424830 | CAAAAAAA others(3): Show |
C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+12052_96+12061d others(12): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424830 | |||||||
| chr2:39424896 | T | C | 1 | a0001c0002t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.96+11996A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424896 | |||||||
| chr2:39424976 | T | A | 34 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(31): Show |
34 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.96+11916A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39424976 | |||||||
| chr2:39425017 | A | G | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.96+11875T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39425017 | |||||||
| chr2:39425029 | C | G | 1 | a0001c0005t0002g0033 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.96+11863G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39425029 | |||||||
| chr2:39425157 | A | C | 31 | a0001c0001t0001g0180 a0001c0001t0002g0027 a0001c0001t0002g0028 others(28): Show |
31 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.96+11735T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39425157 | |||||||
| chr2:39425255 | C | T | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.96+11637G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39425255 | |||||||
| chr2:39425294 | G | GA | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.96+11597dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39425294 | |||||||
| chr2:39425344 | A | G | 166 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(163): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.96+11548T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39425344 | |||||||
| chr2:39425512 | A | G | 3 | a0001c0003t0012g0004 a0001c0004t0005g0002 a0001c0004t0013g0003 |
3 | HG02886.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.96+11380T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39425512 | |||||||
| chr2:39425700 | G | GTA | 135 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(132): Show |
135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.96+11190_96+11191d others(4): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39425700 | |||||||
| chr2:39425831 | T | C | 12 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+11061A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39425831 | |||||||
| chr2:39425996 | T | C | 1 | a0001c0001t0002g0045 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.96+10896A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39425996 | |||||||
| chr2:39426016 | C | G | 10 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(7): Show |
10 | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.96+10876G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39426016 | |||||||
| chr2:39426091 | A | T | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+10801T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39426091 | |||||||
| chr2:39426114 | A | T | 1 | a0001c0003t0004g0227 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.96+10778T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39426114 | |||||||
| chr2:39426184 | C | A | 22 | a0001c0001t0001g0180 a0001c0001t0002g0171 a0001c0001t0003g0173 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.96+10708G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39426184 | |||||||
| chr2:39426193 | T | C | 1 | a0001c0001t0005g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.96+10699A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39426193 | |||||||
| chr2:39426239 | A | G | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.96+10653T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39426239 | |||||||
| chr2:39426242 | C | T | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.96+10650G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39426242 | |||||||
| chr2:39426333 | C | T | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.96+10559G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39426333 | |||||||
| chr2:39426625 | G | A | 2 | a0001c0003t0012g0004 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.96+10267C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39426625 | |||||||
| chr2:39426641 | G | T | 135 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(132): Show |
135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.96+10251C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39426641 | |||||||
| chr2:39426974 | T | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.96+9918A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39426974 | |||||||
| chr2:39427264 | G | A | 1 | a0001c0002t0001g0120 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.96+9628C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39427264 | |||||||
| chr2:39427442 | G | A | 1 | a0001c0002t0010g0213 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.96+9450C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39427442 | |||||||
| chr2:39427647 | G | A | 1 | a0001c0003t0012g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+9245C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39427647 | |||||||
| chr2:39427798 | T | C | 12 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+9094A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39427798 | |||||||
| chr2:39428019 | G | C | 2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.96+8873C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39428019 | |||||||
| chr2:39428073 | A | C | 1 | a0003c0009t0005g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.96+8819T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39428073 | |||||||
| chr2:39428089 | TTA | T | 22 | a0001c0001t0001g0180 a0001c0001t0002g0171 a0001c0001t0003g0173 others(19): Show |
22 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.96+8801_96+8802del others(2): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39428089 | |||||||
| chr2:39428347 | T | C | 1 | a0001c0003t0011g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.96+8545A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39428347 | |||||||
| chr2:39428364 | T | C | 1 | a0001c0003t0004g0222 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.96+8528A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39428364 | |||||||
| chr2:39428423 | C | T | 2 | a0001c0003t0012g0004 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.96+8469G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39428423 | |||||||
| chr2:39428502 | A | G | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.96+8390T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39428502 | |||||||
| chr2:39428593 | T | C | 1 | a0001c0002t0001g0124 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.96+8299A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39428593 | |||||||
| chr2:39428632 | T | C | 211 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(208): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.96+8260A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39428632 | |||||||
| chr2:39428666 | G | A | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.96+8226C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39428666 | |||||||
| chr2:39428682 | C | CA | 17 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(14): Show |
17 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.96+8209dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39428682 | |||||||
| chr2:39428791 | C | T | 2 | a0001c0002t0001g0046 a0001c0002t0001g0047 |
2 | HG01358.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.96+8101G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39428791 | |||||||
| chr2:39429043 | C | T | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.96+7849G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39429043 | |||||||
| chr2:39429064 | C | A | 1 | a0001c0001t0002g0045 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.96+7828G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39429064 | |||||||
| chr2:39429064 | C | CA | 133 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.96+7827dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39429064 | |||||||
| chr2:39429064 | C | CAA | 22 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(19): Show |
22 | HG01433.hp1 HG01934.hp2 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+7826_96+7827dup others(2): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39429064 | |||||||
| chr2:39429064 | CA | C | 10 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0154 others(7): Show |
10 | HG00738.hp2 HG01106.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.96+7827delT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39429064 | |||||||
| chr2:39429064 | CAA | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+7826_96+7827del others(2): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39429064 | |||||||
| chr2:39429187 | G | A | 2 | a0001c0001t0002g0140 a0001c0001t0002g0141 |
2 | NA18945.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.96+7705C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39429187 | |||||||
| chr2:39429196 | T | A | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+7696A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39429196 | |||||||
| chr2:39429206 | A | G | 3 | a0001c0003t0004g0216 a0001c0003t0004g0231 a0001c0003t0004g0232 |
3 | HG02129.hp2 HG02132.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.96+7686T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39429206 | |||||||
| chr2:39429298 | C | T | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.96+7594G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39429298 | |||||||
| chr2:39430065 | G | C | 12 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+6827C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39430065 | |||||||
| chr2:39430078 | T | C | 12 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+6814A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39430078 | |||||||
| chr2:39430210 | C | T | 1 | a0001c0002t0010g0210 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.96+6682G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39430210 | |||||||
| chr2:39430331 | A | T | 1 | a0001c0002t0001g0040 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.96+6561T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39430331 | |||||||
| chr2:39430555 | A | G | 21 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 others(18): Show |
21 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+6337T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39430555 | |||||||
| chr2:39430630 | A | T | 1 | a0001c0002t0001g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.96+6262T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39430630 | |||||||
| chr2:39430798 | C | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.96+6094G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39430798 | |||||||
| chr2:39430945 | T | C | 21 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 others(18): Show |
21 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+5947A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39430945 | |||||||
| chr2:39431326 | T | A | 1 | a0001c0002t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.96+5566A>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39431326 | |||||||
| chr2:39431450 | C | T | 10 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+5442G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39431450 | |||||||
| chr2:39431489 | A | T | 12 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+5403T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39431489 | |||||||
| chr2:39431496 | C | A | 135 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(132): Show |
135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.96+5396G>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39431496 | |||||||
| chr2:39431510 | C | T | 19 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 others(16): Show |
19 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.96+5382G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39431510 | |||||||
| chr2:39431590 | T | C | 16 | a0001c0003t0004g0214 a0001c0003t0004g0215 a0001c0003t0004g0216 others(13): Show |
16 | HG00140.hp1 HG00408.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.96+5302A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39431590 | |||||||
| chr2:39431865 | G | C | 1 | a0002c0010t0005g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.96+5027C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39431865 | |||||||
| chr2:39431953 | G | C | 4 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(1): Show |
4 | HG02258.hp2 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+4939C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39431953 | |||||||
| chr2:39431975 | TAG | T | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.96+4915_96+4916del others(2): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39431975 | |||||||
| chr2:39432240 | G | C | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.96+4652C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39432240 | |||||||
| chr2:39432269 | G | C | 1 | a0001c0001t0002g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.96+4623C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39432269 | |||||||
| chr2:39432381 | T | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.96+4511A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39432381 | |||||||
| chr2:39432586 | G | A | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.96+4306C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39432586 | |||||||
| chr2:39432606 | G | A | 20 | a0001c0001t0015g0192 a0001c0002t0007g0223 a0001c0002t0007g0224 others(17): Show |
20 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.96+4286C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39432606 | |||||||
| chr2:39432913 | G | A | 210 | a0001c0001t0001g0180 a0001c0001t0002g0018 a0001c0001t0002g0019 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.96+3979C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39432913 | |||||||
| chr2:39432983 | T | C | 1 | a0001c0001t0003g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.96+3909A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39432983 | |||||||
| chr2:39433064 | C | T | 10 | a0001c0003t0004g0214 a0001c0003t0004g0216 a0001c0003t0004g0217 others(7): Show |
10 | HG00408.hp1 HG01934.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+3828G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39433064 | |||||||
| chr2:39433098 | A | C | 1 | a0001c0002t0001g0038 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.96+3794T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39433098 | |||||||
| chr2:39433236 | C | G | 135 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(132): Show |
135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.96+3656G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39433236 | |||||||
| chr2:39433252 | A | G | 1 | a0001c0003t0004g0215 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.96+3640T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39433252 | |||||||
| chr2:39433329 | C | T | 1 | a0001c0002t0001g0037 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.96+3563G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39433329 | |||||||
| chr2:39433804 | C | T | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.96+3088G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39433804 | |||||||
| chr2:39433833 | A | T | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+3059T>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39433833 | |||||||
| chr2:39433860 | A | G | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.96+3032T>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39433860 | |||||||
| chr2:39433949 | C | G | 12 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+2943G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39433949 | |||||||
| chr2:39434371 | G | C | 9 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0002t0001g0146 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+2521C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39434371 | |||||||
| chr2:39434668 | G | T | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+2224C>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39434668 | |||||||
| chr2:39434683 | T | C | 19 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 others(16): Show |
19 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.96+2209A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39434683 | |||||||
| chr2:39434810 | T | C | 1 | a0001c0002t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.96+2082A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39434810 | |||||||
| chr2:39435073 | G | C | 1 | a0001c0002t0001g0151 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.96+1819C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39435073 | |||||||
| chr2:39435224 | TC | T | 135 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(132): Show |
135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.96+1667delG | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39435224 | |||||||
| chr2:39435340 | T | C | 12 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+1552A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39435340 | |||||||
| chr2:39435402 | T | C | 21 | a0001c0001t0001g0180 a0001c0001t0003g0173 a0001c0001t0003g0174 others(18): Show |
21 | HG01099.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+1490A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39435402 | |||||||
| chr2:39435413 | T | C | 1 | a0001c0002t0010g0213 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.96+1479A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39435413 | |||||||
| chr2:39435449 | T | C | 1 | a0001c0002t0007g0230 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.96+1443A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39435449 | |||||||
| chr2:39435516 | G | C | 1 | a0001c0001t0015g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.96+1376C>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39435516 | |||||||
| chr2:39435722 | C | T | 10 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+1170G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39435722 | |||||||
| chr2:39435817 | A | C | 2 | a0001c0004t0005g0002 a0001c0004t0013g0003 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.96+1075T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39435817 | |||||||
| chr2:39435979 | T | C | 1 | a0001c0002t0001g0193 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.96+913A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39435979 | |||||||
| chr2:39435982 | ATCCTCAG others(34): Show |
A | 1 | a0001c0001t0003g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.96+869_96+909delAC others(39): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39435982 | |||||||
| chr2:39436068 | T | G | 3 | a0001c0002t0001g0195 a0001c0002t0001g0196 a0001c0002t0001g0197 |
3 | NA18986.hp2 NA19054.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.96+824A>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39436068 | |||||||
| chr2:39436120 | T | C | 8 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0006g0200 others(5): Show |
8 | HG01433.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+772A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39436120 | |||||||
| chr2:39436150 | C | T | 2 | a0001c0003t0005g0005 a0001c0003t0005g0006 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.96+742G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39436150 | |||||||
| chr2:39436193 | C | G | 1 | a0001c0002t0001g0026 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.96+699G>C | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39436193 | |||||||
| chr2:39436258 | A | C | 2 | a0001c0003t0012g0004 a0002c0010t0005g0017 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.96+634T>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39436258 | |||||||
| chr2:39436311 | C | T | 8 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(5): Show |
8 | HG02165.hp1 NA18942.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+581G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39436311 | |||||||
| chr2:39436318 | C | CA | 21 | a0001c0001t0003g0206 a0001c0002t0007g0223 a0001c0002t0007g0224 others(18): Show |
21 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+573dupT | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39436318 | |||||||
| chr2:39436419 | G | A | 12 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+473C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39436419 | |||||||
| chr2:39436554 | C | T | 19 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 others(16): Show |
19 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.96+338G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39436554 | |||||||
| chr2:39436617 | T | C | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.96+275A>G | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39436617 | |||||||
| chr2:39436658 | G | A | 2 | a0001c0003t0004g0231 a0001c0003t0004g0232 |
2 | HG02129.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.96+234C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39436658 | |||||||
| chr2:39436679 | G | A | 1 | a0001c0001t0002g0209 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.96+213C>T | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39436679 | |||||||
| chr2:39436869 | C | T | 21 | a0001c0002t0007g0223 a0001c0002t0007g0224 a0001c0002t0007g0230 others(18): Show |
21 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+23G>A | MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 1/33 | chr2 | 39436869 |