Search by Gene
| geneid | 9020 |
|---|---|
| ensemblid | ENSG00000006062.18 |
| hgncid | 6853 |
| symbol | MAP3K14 |
| name | mitogen-activated protein kinase kinase kinase 14 |
| refseq_nuc | NM_003954.5 |
| refseq_prot | NP_003945.2 |
| ensembl_nuc | ENST00000344686.8 |
| ensembl_prot | ENSP00000478552.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 45263119 |
| end | 45317020 |
| strand | - |
| ver | v1.2 |
| region | chr17:45263119-45317020 |
| region5000 | chr17:45258119-45322020 |
| regionname0 | MAP3K14_chr17_45263119_45317020 |
| regionname5000 | MAP3K14_chr17_45258119_45322020 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 947 | 327 | 89 | 55 | 139 | 14 | 28 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0002 | 0/0 | 947 | 3 | 0 | 3 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0003 | 0/0 | 947 | 3 | 1 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0004 | 0/0 | 947 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0005 | 0/0 | 947 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2844 | 242 | 77 | 39 | 95 | 8 | 22 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| c0002 | 1/0 | 2844 | 81 | 10 | 15 | 43 | 6 | 6 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| c0003 | 0/0 | 2844 | 3 | 0 | 3 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| c0004 | 0/0 | 2844 | 3 | 1 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| c0005 | 0/0 | 2844 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| c0006 | 0/0 | 2844 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| c0007 | 0/0 | 2844 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| c0008 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| c0009 | 0/0 | 2844 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| c0010 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1599 | 152 | 42 | 30 | 64 | 6 | 8 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0002 | 0/0 | 1599 | 119 | 22 | 23 | 53 | 5 | 16 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0003 | 0/0 | 1599 | 20 | 0 | 2 | 17 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0004 | 0/0 | 1599 | 16 | 13 | 1 | 0 | 0 | 2 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0005 | 0/0 | 1599 | 7 | 1 | 4 | 0 | 2 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0006 | 0/0 | 1599 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0007 | 0/0 | 1599 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0008 | 0/0 | 1599 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0009 | 0/0 | 1599 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0010 | 0/0 | 1599 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0011 | 0/0 | 1599 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0012 | 0/0 | 1599 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0013 | 0/0 | 1599 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0014 | 0/0 | 1599 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0015 | 0/0 | 1599 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0016 | 0/0 | 1599 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0017 | 0/0 | 1599 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0018 | 0/0 | 1599 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| t0019 | 0/0 | 1599 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 13 | 2 | 1 | 9 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0002 | 0/0 | 7 | 0 | 3 | 3 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 0/1 | 242 | 77 | 39 | 95 | 8 | 22 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0002 | a0001 | c0002 | 1/0 | 81 | 10 | 15 | 43 | 6 | 6 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0008 | a0001 | c0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0009 | a0001 | c0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0010 | a0001 | c0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0002c0003 | a0002 | c0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0003c0004 | a0003 | c0004 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0004c0005 | a0004 | c0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0005c0007 | a0005 | c0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/1 | 69 | 33 | 11 | 22 | 0 | 2 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 115 | 21 | 21 | 52 | 5 | 16 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 20 | 0 | 2 | 17 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 16 | 13 | 1 | 0 | 0 | 2 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 7 | 1 | 4 | 0 | 2 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0001t0015 | a0001 | c0001 | t0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 1/0 | 75 | 8 | 15 | 39 | 6 | 6 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0002t0006 | a0001 | c0002 | t0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0002t0009 | a0001 | c0002 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0002t0014 | a0001 | c0002 | t0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0002t0016 | a0001 | c0002 | t0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0006t0001 | a0001 | c0006 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0008t0002 | a0001 | c0008 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0009t0001 | a0001 | c0009 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0001c0010t0009 | a0001 | c0010 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0002c0003t0001 | a0002 | c0003 | t0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0003c0004t0001 | a0003 | c0004 | t0001 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0004c0005t0002 | a0004 | c0005 | t0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| a0005c0007t0002 | a0005 | c0007 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0190 | a0001 | c0001 | t0001 | g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0193 | a0001 | c0001 | t0001 | g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0200 | a0001 | c0001 | t0001 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0232 | a0001 | c0001 | t0001 | g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0234 | a0001 | c0001 | t0001 | g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0257 | a0001 | c0001 | t0001 | g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0258 | a0001 | c0001 | t0001 | g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0259 | a0001 | c0001 | t0001 | g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0260 | a0001 | c0001 | t0001 | g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0261 | a0001 | c0001 | t0001 | g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0262 | a0001 | c0001 | t0001 | g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0264 | a0001 | c0001 | t0001 | g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0266 | a0001 | c0001 | t0001 | g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0267 | a0001 | c0001 | t0001 | g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0269 | a0001 | c0001 | t0001 | g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0270 | a0001 | c0001 | t0001 | g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0271 | a0001 | c0001 | t0001 | g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0272 | a0001 | c0001 | t0001 | g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0278 | a0001 | c0001 | t0001 | g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0281 | a0001 | c0001 | t0001 | g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0282 | a0001 | c0001 | t0001 | g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0283 | a0001 | c0001 | t0001 | g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0284 | a0001 | c0001 | t0001 | g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0001g0287 | a0001 | c0001 | t0001 | g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0001 | a0001 | c0001 | t0002 | g0001 | 0/0 | 13 | 2 | 1 | 9 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0002 | a0001 | c0001 | t0002 | g0002 | 0/0 | 7 | 0 | 3 | 3 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0009 | a0001 | c0001 | t0002 | g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0010 | a0001 | c0001 | t0002 | g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0011 | a0001 | c0001 | t0002 | g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0012 | a0001 | c0001 | t0002 | g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0015 | a0001 | c0001 | t0002 | g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0016 | a0001 | c0001 | t0002 | g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0017 | a0001 | c0001 | t0002 | g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0051 | a0001 | c0001 | t0002 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0068 | a0001 | c0001 | t0002 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0071 | a0001 | c0001 | t0002 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0074 | a0001 | c0001 | t0002 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0076 | a0001 | c0001 | t0002 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0077 | a0001 | c0001 | t0002 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0078 | a0001 | c0001 | t0002 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0079 | a0001 | c0001 | t0002 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0081 | a0001 | c0001 | t0002 | g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0083 | a0001 | c0001 | t0002 | g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0085 | a0001 | c0001 | t0002 | g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0086 | a0001 | c0001 | t0002 | g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0088 | a0001 | c0001 | t0002 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0089 | a0001 | c0001 | t0002 | g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0091 | a0001 | c0001 | t0002 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0094 | a0001 | c0001 | t0002 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0095 | a0001 | c0001 | t0002 | g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0096 | a0001 | c0001 | t0002 | g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0097 | a0001 | c0001 | t0002 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0098 | a0001 | c0001 | t0002 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0099 | a0001 | c0001 | t0002 | g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0110 | a0001 | c0001 | t0002 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0111 | a0001 | c0001 | t0002 | g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0113 | a0001 | c0001 | t0002 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0114 | a0001 | c0001 | t0002 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0115 | a0001 | c0001 | t0002 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0117 | a0001 | c0001 | t0002 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0119 | a0001 | c0001 | t0002 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0120 | a0001 | c0001 | t0002 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0121 | a0001 | c0001 | t0002 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0122 | a0001 | c0001 | t0002 | g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0123 | a0001 | c0001 | t0002 | g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0124 | a0001 | c0001 | t0002 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0125 | a0001 | c0001 | t0002 | g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0126 | a0001 | c0001 | t0002 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0127 | a0001 | c0001 | t0002 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0128 | a0001 | c0001 | t0002 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0129 | a0001 | c0001 | t0002 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0130 | a0001 | c0001 | t0002 | g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0131 | a0001 | c0001 | t0002 | g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0132 | a0001 | c0001 | t0002 | g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0133 | a0001 | c0001 | t0002 | g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0134 | a0001 | c0001 | t0002 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0135 | a0001 | c0001 | t0002 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0136 | a0001 | c0001 | t0002 | g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0139 | a0001 | c0001 | t0002 | g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0140 | a0001 | c0001 | t0002 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0141 | a0001 | c0001 | t0002 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0148 | a0001 | c0001 | t0002 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0149 | a0001 | c0001 | t0002 | g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0186 | a0001 | c0001 | t0002 | g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0187 | a0001 | c0001 | t0002 | g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0188 | a0001 | c0001 | t0002 | g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0192 | a0001 | c0001 | t0002 | g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0202 | a0001 | c0001 | t0002 | g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0203 | a0001 | c0001 | t0002 | g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0205 | a0001 | c0001 | t0002 | g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0206 | a0001 | c0001 | t0002 | g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0207 | a0001 | c0001 | t0002 | g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0208 | a0001 | c0001 | t0002 | g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0210 | a0001 | c0001 | t0002 | g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0212 | a0001 | c0001 | t0002 | g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0214 | a0001 | c0001 | t0002 | g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0215 | a0001 | c0001 | t0002 | g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0218 | a0001 | c0001 | t0002 | g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0220 | a0001 | c0001 | t0002 | g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0223 | a0001 | c0001 | t0002 | g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0235 | a0001 | c0001 | t0002 | g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0247 | a0001 | c0001 | t0002 | g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0248 | a0001 | c0001 | t0002 | g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0249 | a0001 | c0001 | t0002 | g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0250 | a0001 | c0001 | t0002 | g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0251 | a0001 | c0001 | t0002 | g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0252 | a0001 | c0001 | t0002 | g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0253 | a0001 | c0001 | t0002 | g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0254 | a0001 | c0001 | t0002 | g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0256 | a0001 | c0001 | t0002 | g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0263 | a0001 | c0001 | t0002 | g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0275 | a0001 | c0001 | t0002 | g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0285 | a0001 | c0001 | t0002 | g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0002g0286 | a0001 | c0001 | t0002 | g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0004 | a0001 | c0001 | t0003 | g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0008 | a0001 | c0001 | t0003 | g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0042 | a0001 | c0001 | t0003 | g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0072 | a0001 | c0001 | t0003 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0073 | a0001 | c0001 | t0003 | g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0080 | a0001 | c0001 | t0003 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0082 | a0001 | c0001 | t0003 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0100 | a0001 | c0001 | t0003 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0101 | a0001 | c0001 | t0003 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0102 | a0001 | c0001 | t0003 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0104 | a0001 | c0001 | t0003 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0105 | a0001 | c0001 | t0003 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0106 | a0001 | c0001 | t0003 | g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0108 | a0001 | c0001 | t0003 | g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0109 | a0001 | c0001 | t0003 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0181 | a0001 | c0001 | t0003 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0003g0182 | a0001 | c0001 | t0003 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0004g0018 | a0001 | c0001 | t0004 | g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0004g0019 | a0001 | c0001 | t0004 | g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0004g0059 | a0001 | c0001 | t0004 | g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0004g0087 | a0001 | c0001 | t0004 | g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0004g0233 | a0001 | c0001 | t0004 | g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0004g0276 | a0001 | c0001 | t0004 | g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0004g0288 | a0001 | c0001 | t0004 | g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0004g0289 | a0001 | c0001 | t0004 | g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0004g0290 | a0001 | c0001 | t0004 | g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0004g0291 | a0001 | c0001 | t0004 | g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0004g0292 | a0001 | c0001 | t0004 | g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0004g0293 | a0001 | c0001 | t0004 | g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0004g0294 | a0001 | c0001 | t0004 | g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0004g0296 | a0001 | c0001 | t0004 | g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0005g0143 | a0001 | c0001 | t0005 | g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0005g0155 | a0001 | c0001 | t0005 | g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0005g0169 | a0001 | c0001 | t0005 | g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0005g0170 | a0001 | c0001 | t0005 | g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0005g0171 | a0001 | c0001 | t0005 | g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0005g0183 | a0001 | c0001 | t0005 | g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0005g0184 | a0001 | c0001 | t0005 | g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0007g0236 | a0001 | c0001 | t0007 | g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0007g0237 | a0001 | c0001 | t0007 | g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0007g0238 | a0001 | c0001 | t0007 | g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0008g0199 | a0001 | c0001 | t0008 | g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0008g0217 | a0001 | c0001 | t0008 | g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0010g0279 | a0001 | c0001 | t0010 | g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0010g0280 | a0001 | c0001 | t0010 | g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0011g0084 | a0001 | c0001 | t0011 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0011g0092 | a0001 | c0001 | t0011 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0012g0107 | a0001 | c0001 | t0012 | g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0013g0093 | a0001 | c0001 | t0013 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0015g0189 | a0001 | c0001 | t0015 | g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0017g0156 | a0001 | c0001 | t0017 | g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0018g0090 | a0001 | c0001 | t0018 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0001t0019g0216 | a0001 | c0001 | t0019 | g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0003 | a0001 | c0002 | t0001 | g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0005 | a0001 | c0002 | t0001 | g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0006 | a0001 | c0002 | t0001 | g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0007 | a0001 | c0002 | t0001 | g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0014 | a0001 | c0002 | t0001 | g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0023 | a0001 | c0002 | t0001 | g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0024 | a0001 | c0002 | t0001 | g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0027 | a0001 | c0002 | t0001 | g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0028 | a0001 | c0002 | t0001 | g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0029 | a0001 | c0002 | t0001 | g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0030 | a0001 | c0002 | t0001 | g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0031 | a0001 | c0002 | t0001 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0032 | a0001 | c0002 | t0001 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0033 | a0001 | c0002 | t0001 | g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0034 | a0001 | c0002 | t0001 | g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0035 | a0001 | c0002 | t0001 | g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0036 | a0001 | c0002 | t0001 | g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0037 | a0001 | c0002 | t0001 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0038 | a0001 | c0002 | t0001 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0039 | a0001 | c0002 | t0001 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0040 | a0001 | c0002 | t0001 | g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0041 | a0001 | c0002 | t0001 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0044 | a0001 | c0002 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0045 | a0001 | c0002 | t0001 | g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0046 | a0001 | c0002 | t0001 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0047 | a0001 | c0002 | t0001 | g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0048 | a0001 | c0002 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0049 | a0001 | c0002 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0050 | a0001 | c0002 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0054 | a0001 | c0002 | t0001 | g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0057 | a0001 | c0002 | t0001 | g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0058 | a0001 | c0002 | t0001 | g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0062 | a0001 | c0002 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0063 | a0001 | c0002 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0070 | a0001 | c0002 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0075 | a0001 | c0002 | t0001 | g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0103 | a0001 | c0002 | t0001 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0112 | a0001 | c0002 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0116 | a0001 | c0002 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0118 | a0001 | c0002 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0194 | a0001 | c0002 | t0001 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0195 | a0001 | c0002 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0196 | a0001 | c0002 | t0001 | g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0198 | a0001 | c0002 | t0001 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0204 | a0001 | c0002 | t0001 | g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0209 | a0001 | c0002 | t0001 | g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0211 | a0001 | c0002 | t0001 | g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0213 | a0001 | c0002 | t0001 | g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0221 | a0001 | c0002 | t0001 | g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0222 | a0001 | c0002 | t0001 | g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0228 | a0001 | c0002 | t0001 | g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0229 | a0001 | c0002 | t0001 | g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0230 | a0001 | c0002 | t0001 | g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0231 | a0001 | c0002 | t0001 | g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0239 | a0001 | c0002 | t0001 | g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0240 | a0001 | c0002 | t0001 | g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0241 | a0001 | c0002 | t0001 | g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0242 | a0001 | c0002 | t0001 | g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0243 | a0001 | c0002 | t0001 | g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0244 | a0001 | c0002 | t0001 | g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0245 | a0001 | c0002 | t0001 | g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0246 | a0001 | c0002 | t0001 | g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0268 | a0001 | c0002 | t0001 | g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0273 | a0001 | c0002 | t0001 | g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0274 | a0001 | c0002 | t0001 | g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0001g0295 | a0001 | c0002 | t0001 | g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0006g0055 | a0001 | c0002 | t0006 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0006g0056 | a0001 | c0002 | t0006 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0006g0185 | a0001 | c0002 | t0006 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0009g0265 | a0001 | c0002 | t0009 | g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0014g0060 | a0001 | c0002 | t0014 | g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0002t0016g0150 | a0001 | c0002 | t0016 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0006t0001g0227 | a0001 | c0006 | t0001 | g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0008t0002g0277 | a0001 | c0008 | t0002 | g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0009t0001g0219 | a0001 | c0009 | t0001 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0001c0010t0009g0255 | a0001 | c0010 | t0009 | g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0002c0003t0001g0224 | a0002 | c0003 | t0001 | g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0002c0003t0001g0225 | a0002 | c0003 | t0001 | g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0002c0003t0001g0226 | a0002 | c0003 | t0001 | g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0003c0004t0001g0025 | a0003 | c0004 | t0001 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0003c0004t0001g0052 | a0003 | c0004 | t0001 | g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0003c0004t0001g0053 | a0003 | c0004 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0004c0005t0002g0137 | a0004 | c0005 | t0002 | g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0004c0005t0002g0138 | a0004 | c0005 | t0002 | g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| a0005c0007t0002g0197 | a0005 | c0007 | t0002 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | GBR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0169 | EUR | GBR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0230 | EUR | GBR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0171 | EUR | GBR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0017 | EUR | FIN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0007 | EUR | FIN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0241 | EUR | FIN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0253 | EUR | FIN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00597 | hp2 | a0001 | c0001 | t0011 | g0084 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0170 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0242 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0209 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01167 | hp2 | a0004 | c0005 | t0002 | g0138 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0183 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0184 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01169 | hp2 | a0004 | c0005 | t0002 | g0137 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0155 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0224 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01358 | hp2 | a0002 | c0003 | t0001 | g0225 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01361 | hp1 | a0001 | c0006 | t0001 | g0227 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0231 | EUR | IBS | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0254 | EUR | IBS | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0290 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02004 | hp2 | a0002 | c0003 | t0001 | g0226 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0143 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | CDX | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | CDX | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0213 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0199 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0288 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0273 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02647 | hp1 | a0001 | c0008 | t0002 | g0277 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0236 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0237 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0276 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0280 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0238 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02886 | hp1 | a0001 | c0001 | t0015 | g0189 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0291 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0293 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0222 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0294 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0295 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0217 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0229 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0289 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03516 | hp2 | a0003 | c0004 | t0001 | g0025 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0116 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03669 | hp2 | a0001 | c0001 | t0017 | g0156 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | BEB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | BEB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | BEB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0211 | SAS | STU | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | STU | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0087 | SAS | STU | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | STU | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0239 | SAS | STU | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | YRI | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0292 | AFR | YRI | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | CHB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | CHB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | YRI | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | YRI | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18948 | hp2 | a0001 | c0001 | t0011 | g0092 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18949 | hp2 | a0001 | c0001 | t0018 | g0090 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18956 | hp1 | a0001 | c0002 | t0006 | g0185 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18974 | hp1 | a0001 | c0001 | t0013 | g0093 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18998 | hp1 | a0003 | c0004 | t0001 | g0052 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19002 | hp2 | a0001 | c0002 | t0006 | g0056 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19004 | hp1 | a0001 | c0002 | t0006 | g0055 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19011 | hp1 | a0001 | c0009 | t0001 | g0219 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0296 | AFR | LWK | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19030 | hp2 | a0001 | c0002 | t0009 | g0265 | AFR | LWK | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19043 | hp1 | a0001 | c0002 | t0016 | g0150 | AFR | LWK | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | LWK | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19065 | hp2 | a0005 | c0007 | t0002 | g0197 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19081 | hp2 | a0001 | c0002 | t0014 | g0060 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19085 | hp2 | a0003 | c0004 | t0001 | g0053 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | YRI | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | YRI | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | ASW | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ASW | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0006 | EUR | TSI | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | TSI | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA20805 | hp2 | a0001 | c0001 | t0012 | g0107 | EUR | TSI | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | GIH | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0204 | SAS | GIH | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0279 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0233 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| HG03471 | hp2 | a0001 | c0010 | t0009 | g0255 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | USA | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | LWK | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| NA21309 | hp2 | a0001 | c0001 | t0019 | g0216 | AFR | LWK | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0158 | REF | REF | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0075 | REF | REF | MAP3K14_chr17_45258119_45322020 | MAP3K14 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45267660
|
C | G | 1 | a0005 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.2072G>C | p.Arg691Thr | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 12/16 | 2153/4442 | 2072/2844 | 691/947 | chr17 | 45267660 | ||
| chr17:45286809
|
G | C | 1 | a0004 | 2 | HG01167.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.774C>G | p.Phe258Leu | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/16 | 855/4442 | 774/2844 | 258/947 | chr17 | 45286809 | ||
| chr17:45286819
|
G | A | 1 | a0003 | 3 | HG03516.hp2 NA18998.hp1 NA19085.hp2 |
missense_variant | MODERATE | c.764C>T | p.Thr255Met | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/16 | 845/4442 | 764/2844 | 255/947 | chr17 | 45286819 | ||
| chr17:45287272
|
C | T | 1 | a0002 | 3 | HG01256.hp2 HG01358.hp2 HG02004.hp2 |
missense_variant | MODERATE | c.419G>A | p.Ser140Asn | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 4/16 | 500/4442 | 419/2844 | 140/947 | chr17 | 45287272 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45264774
|
G | C | 4 | a0001c0001a0001c0008a0004c0005others(1): Show | 246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
synonymous_variant | LOW | c.2706C>G | p.Val902Val | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 2787/4442 | 2706/2844 | 902/947 | chr17 | 45264774 | ||
| chr17:45267425
|
T | C | 1 | a0001c0010 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.2307A>G | p.Glu769Glu | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 12/16 | 2388/4442 | 2307/2844 | 769/947 | chr17 | 45267425 | ||
| chr17:45267434
|
C | T | 1 | a0001c0009 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.2298G>A | p.Pro766Pro | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 12/16 | 2379/4442 | 2298/2844 | 766/947 | chr17 | 45267434 | ||
| chr17:45267629
|
C | T | 1 | a0001c0008 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.2103G>A | p.Arg701Arg | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 12/16 | 2184/4442 | 2103/2844 | 701/947 | chr17 | 45267629 | ||
| chr17:45290578
|
C | T | 1 | a0001c0006 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.168G>A | p.Glu56Glu | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/16 | 249/4442 | 168/2844 | 56/947 | chr17 | 45290578 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45263226
|
G | A | 2 | a0001c0001t0007a0001c0001t0010 | 5 | HG02486.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1410C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 1410 | chr17 | 45263226 | |||||
| chr17:45263239
|
C | T | 1 | a0001c0001t0018 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1397G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 1397 | chr17 | 45263239 | |||||
| chr17:45263264
|
C | T | 1 | a0001c0001t0005 | 7 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1372G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 1372 | chr17 | 45263264 | |||||
| chr17:45263342
|
G | A | 2 | a0001c0002t0009a0001c0010t0009 | 2 | HG03471.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1294C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 1294 | chr17 | 45263342 | |||||
| chr17:45263460
|
T | C | 1 | a0001c0001t0010 | 2 | HG02486.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1176A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 1176 | chr17 | 45263460 | |||||
| chr17:45263569
|
G | A | 9 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(6): Show | 141 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1067C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 1067 | chr17 | 45263569 | |||||
| chr17:45263743
|
C | T | 2 | a0001c0001t0003a0001c0001t0012 | 21 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*893G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 893 | chr17 | 45263743 | |||||
| chr17:45263758
|
C | T | 1 | a0001c0001t0017 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*878G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 878 | chr17 | 45263758 | |||||
| chr17:45263951
|
A | G | 1 | a0001c0002t0016 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*685T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 685 | chr17 | 45263951 | |||||
| chr17:45263992
|
A | G | 1 | a0001c0001t0004 | 16 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*644T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 644 | chr17 | 45263992 | |||||
| chr17:45264099
|
G | T | 1 | a0001c0001t0015 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*537C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 537 | chr17 | 45264099 | |||||
| chr17:45264174
|
C | T | 1 | a0001c0002t0014 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*462G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 462 | chr17 | 45264174 | |||||
| chr17:45264248
|
C | T | 1 | a0001c0002t0006 | 3 | NA18956.hp1 NA19002.hp2 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*388G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 388 | chr17 | 45264248 | |||||
| chr17:45264526
|
C | T | 1 | a0001c0001t0013 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*110G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 110 | chr17 | 45264526 | |||||
| chr17:45264535
|
G | A | 1 | a0001c0001t0012 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 101 | chr17 | 45264535 | |||||
| chr17:45264546
|
G | T | 2 | a0001c0001t0003a0001c0001t0012 | 21 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*90C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 90 | chr17 | 45264546 | |||||
| chr17:45264585
|
C | T | 1 | a0001c0001t0008 | 2 | HG02258.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*51G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 51 | chr17 | 45264585 | |||||
| chr17:45264605
|
G | A | 1 | a0001c0001t0019 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*31C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 31 | chr17 | 45264605 | |||||
| chr17:45264610
|
T | C | 1 | a0001c0001t0011 | 2 | HG00597.hp2 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*26A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 26 | chr17 | 45264610 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45264939
|
C | A | 109 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0009others(106): Show | 136 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2680-139G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 15/15 | chr17 | 45264939 | ||||||
| chr17:45265033
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2679+130G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 15/15 | chr17 | 45265033 | ||||||
| chr17:45265293
|
G | C | 2 | a0001c0001t0005g0143a0001c0001t0005g0171 | 2 | HG00140.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.2579-30C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45265293 | ||||||
| chr17:45265531
|
G | A | 1 | a0001c0001t0015g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2579-268C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45265531 | ||||||
| chr17:45265626
|
C | CG | 74 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(71): Show | 75 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.2579-364dupC | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45265626 | ||||||
| chr17:45265752
|
T | C | 1 | a0001c0001t0003g0108 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2579-489A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45265752 | ||||||
| chr17:45265799
|
C | T | 17 | a0001c0001t0001g0022a0001c0001t0001g0190a0001c0001t0001g0191others(14): Show | 17 | HG01891.hp2 HG02280.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.2579-536G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45265799 | ||||||
| chr17:45265882
|
T | C | 18 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0042others(15): Show | 21 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.2579-619A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45265882 | ||||||
| chr17:45265950
|
A | G | 2 | a0001c0001t0005g0143a0001c0001t0005g0171 | 2 | HG00140.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.2578+587T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45265950 | ||||||
| chr17:45266016
|
C | T | 2 | a0003c0004t0001g0052a0003c0004t0001g0053 | 2 | NA18998.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2578+521G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45266016 | ||||||
| chr17:45266310
|
A | G | 1 | a0001c0002t0001g0049 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2578+227T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45266310 | ||||||
| chr17:45266314
|
G | A | 1 | a0001c0001t0002g0129 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2578+223C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45266314 | ||||||
| chr17:45266480
|
G | A | 18 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(15): Show | 18 | HG02145.hp1 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.2578+57C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45266480 | ||||||
| chr17:45266691
|
C | T | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2434-10G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 13/15 | chr17 | 45266691 | ||||||
| chr17:45266706
|
G | A | 127 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0258others(124): Show | 157 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2434-25C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 13/15 | chr17 | 45266706 | ||||||
| chr17:45266737
|
C | T | 1 | a0001c0001t0002g0285 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2434-56G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 13/15 | chr17 | 45266737 | ||||||
| chr17:45266766
|
C | T | 1 | a0001c0001t0017g0156 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2434-85G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 13/15 | chr17 | 45266766 | ||||||
| chr17:45268090
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1973-331C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268090 | ||||||
| chr17:45268099
|
C | T | 3 | a0001c0001t0002g0111a0001c0001t0002g0136a0001c0001t0002g0207 | 3 | HG01109.hp1 HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1973-340G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268099 | ||||||
| chr17:45268174
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1973-415G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268174 | ||||||
| chr17:45268183
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1973-424G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268183 | ||||||
| chr17:45268187
|
T | C | 1 | a0001c0001t0002g0215 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1973-428A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268187 | ||||||
| chr17:45268328
|
C | A | 1 | a0001c0001t0002g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1973-569G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268328 | ||||||
| chr17:45268491
|
G | A | 14 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0059others(11): Show | 16 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1973-732C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268491 | ||||||
| chr17:45268593
|
G | T | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1973-834C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268593 | ||||||
| chr17:45268706
|
C | T | 1 | a0001c0002t0001g0204 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1973-947G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268706 | ||||||
| chr17:45269057
|
C | T | 1 | a0001c0001t0019g0216 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1973-1298G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269057 | ||||||
| chr17:45269102
|
G | A | 1 | a0001c0001t0015g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1972+1311C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269102 | ||||||
| chr17:45269126
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1972+1287G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269126 | ||||||
| chr17:45269256
|
C | T | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1972+1157G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269256 | ||||||
| chr17:45269264
|
A | C | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1972+1149T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269264 | ||||||
| chr17:45269265
|
G | C | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1972+1148C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269265 | ||||||
| chr17:45269266
|
C | T | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1972+1147G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269266 | ||||||
| chr17:45269268
|
T | C | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1972+1145A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269268 | ||||||
| chr17:45269542
|
C | T | 1 | a0001c0002t0001g0070 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1972+871G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269542 | ||||||
| chr17:45269611
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1972+802C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269611 | ||||||
| chr17:45269613
|
G | T | 259 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(256): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1972+800C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269613 | ||||||
| chr17:45269617
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1972+796G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269617 | ||||||
| chr17:45269632
|
A | G | 1 | a0001c0001t0004g0292 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1972+781T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269632 | ||||||
| chr17:45269699
|
T | C | 35 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0030others(32): Show | 39 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1972+714A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269699 | ||||||
| chr17:45269969
|
C | G | 258 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(255): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.1972+444G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269969 | ||||||
| chr17:45270243
|
C | T | 74 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0043others(71): Show | 75 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1972+170G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45270243 | ||||||
| chr17:45270598
|
T | A | 1 | a0001c0001t0002g0208 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1822-35A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 10/15 | chr17 | 45270598 | ||||||
| chr17:45270618
|
G | C | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1822-55C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 10/15 | chr17 | 45270618 | ||||||
| chr17:45270975
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1821+83C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 10/15 | chr17 | 45270975 | ||||||
| chr17:45271028
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1821+30G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 10/15 | chr17 | 45271028 | ||||||
| chr17:45271041
|
T | G | 13 | a0001c0001t0001g0193a0001c0001t0001g0262a0001c0001t0001g0266others(10): Show | 13 | HG02280.hp1 HG02486.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1821+17A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 10/15 | chr17 | 45271041 | ||||||
| chr17:45271045
|
T | G | 13 | a0001c0001t0001g0193a0001c0001t0001g0262a0001c0001t0001g0266others(10): Show | 13 | HG02280.hp1 HG02486.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1821+13A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 10/15 | chr17 | 45271045 | ||||||
| chr17:45271367
|
A | G | 2 | a0001c0001t0002g0051a0001c0001t0002g0127 | 2 | NA18994.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1658-146T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45271367 | ||||||
| chr17:45271407
|
G | A | 7 | a0001c0001t0001g0257a0001c0001t0001g0259a0001c0001t0001g0260others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1658-186C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45271407 | ||||||
| chr17:45271520
|
G | A | 260 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(257): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1658-299C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45271520 | ||||||
| chr17:45271751
|
A | G | 1 | a0001c0001t0002g0126 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1658-530T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45271751 | ||||||
| chr17:45271809
|
G | A | 88 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(85): Show | 89 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1658-588C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45271809 | ||||||
| chr17:45271830
|
G | T | 8 | a0001c0002t0001g0014a0001c0002t0001g0194a0001c0002t0001g0195others(5): Show | 9 | HG00673.hp1 HG02083.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1658-609C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45271830 | ||||||
| chr17:45272362
|
A | AT | 44 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0043others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1657+1140dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45272362 | ||||||
| chr17:45272515
|
T | C | 35 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0030others(32): Show | 39 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1657+988A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45272515 | ||||||
| chr17:45272553
|
G | T | 260 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(257): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1657+950C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45272553 | ||||||
| chr17:45272714
|
C | T | 35 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0030others(32): Show | 39 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1657+789G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45272714 | ||||||
| chr17:45273109
|
C | T | 1 | a0001c0001t0004g0276 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1657+394G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45273109 | ||||||
| chr17:45273147
|
G | A | 88 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(85): Show | 89 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1657+356C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45273147 | ||||||
| chr17:45273299
|
A | G | 115 | a0001c0001t0001g0022a0001c0001t0001g0200a0001c0001t0001g0201others(112): Show | 142 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1657+204T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45273299 | ||||||
| chr17:45273396
|
C | T | 3 | a0001c0002t0001g0023a0001c0002t0001g0024a0003c0004t0001g0025 | 3 | HG01069.hp1 HG01071.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1657+107G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45273396 | ||||||
| chr17:45273403
|
G | T | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1657+100C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45273403 | ||||||
| chr17:45273470
|
T | C | 8 | a0001c0001t0001g0193a0001c0001t0001g0262a0001c0001t0001g0266others(5): Show | 8 | HG02280.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1657+33A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45273470 | ||||||
| chr17:45273634
|
G | A | 2 | a0001c0002t0001g0268a0001c0002t0001g0273 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1553-27C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 8/15 | chr17 | 45273634 | ||||||
| chr17:45273672
|
C | G | 35 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0030others(32): Show | 39 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1553-65G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 8/15 | chr17 | 45273672 | ||||||
| chr17:45273707
|
T | C | 1 | a0001c0001t0003g0004 | 3 | NA18955.hp1 NA18962.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1553-100A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 8/15 | chr17 | 45273707 | ||||||
| chr17:45273760
|
G | C | 115 | a0001c0001t0001g0022a0001c0001t0001g0200a0001c0001t0001g0201others(112): Show | 142 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1553-153C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 8/15 | chr17 | 45273760 | ||||||
| chr17:45273867
|
C | T | 1 | a0001c0001t0002g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1552+256G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 8/15 | chr17 | 45273867 | ||||||
| chr17:45274290
|
G | C | 4 | a0001c0001t0001g0026a0001c0001t0001g0152a0001c0001t0001g0172others(1): Show | 4 | HG01106.hp1 HG02056.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1421-36C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 7/15 | chr17 | 45274290 | ||||||
| chr17:45274682
|
C | T | 43 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0043others(40): Show | 44 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1291-89G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45274682 | ||||||
| chr17:45274714
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1291-121G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45274714 | ||||||
| chr17:45274764
|
G | T | 1 | a0001c0001t0002g0125 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1291-171C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45274764 | ||||||
| chr17:45274854
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1291-261G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45274854 | ||||||
| chr17:45274953
|
C | T | 1 | a0001c0002t0001g0295 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1291-360G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45274953 | ||||||
| chr17:45275090
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1291-497C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275090 | ||||||
| chr17:45275100
|
G | C | 1 | a0001c0001t0001g0260 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1291-507C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275100 | ||||||
| chr17:45275103
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1291-510G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275103 | ||||||
| chr17:45275260
|
G | A | 1 | a0001c0001t0002g0085 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1291-667C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275260 | ||||||
| chr17:45275275
|
T | C | 147 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(144): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1291-682A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275275 | ||||||
| chr17:45275356
|
T | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1291-763A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275356 | ||||||
| chr17:45275386
|
T | C | 2 | a0004c0005t0002g0137a0004c0005t0002g0138 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1291-793A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275386 | ||||||
| chr17:45275482
|
CA | C | 111 | a0001c0001t0001g0022a0001c0001t0001g0200a0001c0001t0001g0201others(108): Show | 138 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1291-890delT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275482 | ||||||
| chr17:45275489
|
AAAAAAC | A | 126 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0043others(123): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1291-902_1291-897d others(8): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275489 | ||||||
| chr17:45275490
|
AAAAAC | A | 19 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0146others(16): Show | 19 | HG00621.hp1 HG00741.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1291-902_1291-898d others(7): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275490 | ||||||
| chr17:45275536
|
C | A | 1 | a0001c0001t0019g0216 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1291-943G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275536 | ||||||
| chr17:45275752
|
TTTC | T | 43 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0043others(40): Show | 44 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1291-1162_1291-116 others(7): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275752 | ||||||
| chr17:45275760
|
CT | C | 144 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(141): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1291-1168delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275760 | ||||||
| chr17:45275765
|
T | C | 13 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0042others(10): Show | 16 | HG00438.hp2 HG00621.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1291-1172A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275765 | ||||||
| chr17:45275868
|
T | TCTCCTGC others(16): Show |
1 | a0001c0002t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1291-1298_1291-127 others(27): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275868 | ||||||
| chr17:45275902
|
C | T | 76 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0043others(73): Show | 77 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1291-1309G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275902 | ||||||
| chr17:45275936
|
A | G | 1 | a0001c0001t0013g0093 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1291-1343T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275936 | ||||||
| chr17:45276041
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1291-1448C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276041 | ||||||
| chr17:45276056
|
C | T | 147 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(144): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1291-1463G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276056 | ||||||
| chr17:45276204
|
C | A | 3 | a0001c0001t0002g0256a0001c0002t0009g0265a0001c0010t0009g0255 | 3 | HG01243.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1291-1611G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276204 | ||||||
| chr17:45276279
|
T | A | 13 | a0001c0001t0001g0193a0001c0001t0001g0262a0001c0001t0001g0266others(10): Show | 13 | HG02280.hp1 HG02486.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1291-1686A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276279 | ||||||
| chr17:45276310
|
G | A | 112 | a0001c0001t0001g0022a0001c0001t0001g0200a0001c0001t0001g0201others(109): Show | 139 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1291-1717C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276310 | ||||||
| chr17:45276359
|
A | G | 1 | a0001c0001t0002g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1291-1766T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276359 | ||||||
| chr17:45276396
|
C | T | 78 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(75): Show | 79 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1291-1803G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276396 | ||||||
| chr17:45276517
|
CT | C | 76 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0043others(73): Show | 77 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1291-1925delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276517 | ||||||
| chr17:45276551
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1291-1958C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276551 | ||||||
| chr17:45276823
|
C | CT | 39 | a0001c0001t0001g0020a0001c0001t0001g0193a0001c0001t0001g0258others(36): Show | 42 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1291-2231dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276823 | ||||||
| chr17:45276823
|
C | CTT | 53 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0061others(50): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.1291-2232_1291-223 others(6): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276823 | ||||||
| chr17:45276823
|
C | CTTT | 16 | a0001c0001t0001g0026a0001c0001t0001g0142a0001c0001t0001g0145others(13): Show | 16 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1291-2233_1291-223 others(7): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276823 | ||||||
| chr17:45276823
|
CT | C | 99 | a0001c0001t0001g0022a0001c0001t0001g0200a0001c0001t0001g0234others(96): Show | 126 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1291-2231delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276823 | ||||||
| chr17:45276823
|
CTT | C | 6 | a0001c0001t0002g0078a0001c0001t0002g0091a0001c0001t0002g0094others(3): Show | 6 | HG02896.hp2 NA18747.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291-2232_1291-223 others(6): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276823 | ||||||
| chr17:45276932
|
C | T | 4 | a0001c0001t0002g0076a0001c0001t0002g0091a0001c0001t0002g0134others(1): Show | 4 | NA18939.hp1 NA18943.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291-2339G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276932 | ||||||
| chr17:45276992
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1291-2399C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276992 | ||||||
| chr17:45277152
|
T | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0167 | 2 | NA18969.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1291-2559A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277152 | ||||||
| chr17:45277153
|
A | C | 2 | a0001c0001t0002g0123a0001c0001t0002g0130 | 2 | HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1291-2560T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277153 | ||||||
| chr17:45277250
|
C | T | 33 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0030others(30): Show | 37 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1291-2657G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277250 | ||||||
| chr17:45277314
|
G | A | 135 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1291-2721C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277314 | ||||||
| chr17:45277501
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1291-2908C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277501 | ||||||
| chr17:45277563
|
G | A | 80 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(77): Show | 81 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1291-2970C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277563 | ||||||
| chr17:45277729
|
C | T | 1 | a0001c0001t0002g0188 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1291-3136G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277729 | ||||||
| chr17:45277795
|
G | A | 2 | a0001c0002t0001g0028a0001c0002t0001g0029 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1291-3202C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277795 | ||||||
| chr17:45278360
|
G | C | 1 | a0001c0001t0002g0122 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1291-3767C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45278360 | ||||||
| chr17:45278679
|
C | CT | 23 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(20): Show | 23 | HG00642.hp2 HG02145.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291-4087dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45278679 | ||||||
| chr17:45278679
|
C | CTTT | 11 | a0001c0001t0001g0258a0001c0001t0002g0256a0001c0002t0001g0023others(8): Show | 11 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1291-4089_1291-408 others(7): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45278679 | ||||||
| chr17:45278679
|
CT | C | 17 | a0001c0001t0001g0177a0001c0001t0001g0193a0001c0001t0001g0262others(14): Show | 17 | HG01256.hp1 HG02109.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1291-4087delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45278679 | ||||||
| chr17:45279407
|
G | A | 10 | a0001c0001t0001g0258a0001c0001t0002g0256a0001c0002t0001g0023others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1291-4814C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45279407 | ||||||
| chr17:45279425
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1291-4832G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45279425 | ||||||
| chr17:45279494
|
A | G | 1 | a0001c0002t0001g0194 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1291-4901T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45279494 | ||||||
| chr17:45279525
|
C | T | 2 | a0003c0004t0001g0052a0003c0004t0001g0053 | 2 | NA18998.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1291-4932G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45279525 | ||||||
| chr17:45279536
|
G | A | 2 | a0001c0001t0008g0199a0001c0001t0008g0217 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1291-4943C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45279536 | ||||||
| chr17:45279675
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1291-5082C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45279675 | ||||||
| chr17:45279797
|
A | G | 1 | a0001c0001t0017g0156 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1290+5015T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45279797 | ||||||
| chr17:45280299
|
C | CT | 47 | a0001c0001t0001g0020a0001c0001t0001g0065a0001c0001t0001g0066others(44): Show | 47 | HG00558.hp2 HG00642.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1290+4512dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280299 | ||||||
| chr17:45280299
|
C | CTT | 35 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0043others(32): Show | 36 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.1290+4511_1290+451 others(6): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280299 | ||||||
| chr17:45280299
|
C | CTTT | 15 | a0001c0001t0001g0151a0001c0001t0001g0157a0001c0001t0001g0160others(12): Show | 15 | HG01433.hp1 HG02055.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1290+4510_1290+451 others(7): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280299 | ||||||
| chr17:45280299
|
C | CTTTT | 6 | a0001c0001t0001g0142a0001c0001t0001g0172a0001c0001t0001g0178others(3): Show | 6 | HG00741.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1290+4509_1290+451 others(8): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280299 | ||||||
| chr17:45280299
|
CT | C | 13 | a0001c0001t0001g0281a0001c0001t0002g0129a0001c0001t0002g0205others(10): Show | 14 | HG00673.hp1 HG02083.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.1290+4512delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280299 | ||||||
| chr17:45280342
|
C | T | 10 | a0001c0001t0001g0258a0001c0001t0002g0256a0001c0002t0001g0023others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1290+4470G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280342 | ||||||
| chr17:45280437
|
G | C | 36 | a0001c0001t0003g0042a0001c0002t0001g0003a0001c0002t0001g0007others(33): Show | 40 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1290+4375C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280437 | ||||||
| chr17:45280452
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1290+4360G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280452 | ||||||
| chr17:45280503
|
C | T | 1 | a0001c0002t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4309G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280503 | ||||||
| chr17:45280533
|
G | A | 13 | a0001c0001t0001g0193a0001c0001t0001g0262a0001c0001t0001g0266others(10): Show | 13 | HG02280.hp1 HG02486.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1290+4279C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280533 | ||||||
| chr17:45280535
|
C | G | 1 | a0001c0002t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4277G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280535 | ||||||
| chr17:45280536
|
C | A | 1 | a0001c0002t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4276G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280536 | ||||||
| chr17:45280538
|
C | A | 1 | a0001c0002t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4274G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280538 | ||||||
| chr17:45280544
|
A | G | 1 | a0001c0002t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4268T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280544 | ||||||
| chr17:45280546
|
T | A | 1 | a0001c0002t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4266A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280546 | ||||||
| chr17:45280547
|
CACCCGCC others(3): Show |
C | 1 | a0001c0002t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4255_1290+426 others(14): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280547 | ||||||
| chr17:45280559
|
C | T | 1 | a0001c0002t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4253G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280559 | ||||||
| chr17:45280560
|
C | G | 1 | a0001c0002t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4252G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280560 | ||||||
| chr17:45280562
|
C | G | 1 | a0001c0002t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4250G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280562 | ||||||
| chr17:45280563
|
T | G | 1 | a0001c0002t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4249A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280563 | ||||||
| chr17:45280564
|
C | T | 1 | a0001c0002t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4248G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280564 | ||||||
| chr17:45280571
|
C | T | 18 | a0001c0001t0002g0081a0001c0001t0003g0004a0001c0001t0003g0008others(15): Show | 21 | HG00408.hp1 HG00621.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1290+4241G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280571 | ||||||
| chr17:45280799
|
C | T | 111 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(108): Show | 115 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1290+4013G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280799 | ||||||
| chr17:45280812
|
T | C | 1 | a0001c0002t0001g0204 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1290+4000A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280812 | ||||||
| chr17:45280857
|
C | T | 2 | a0001c0001t0002g0275a0001c0001t0015g0189 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1290+3955G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280857 | ||||||
| chr17:45280858
|
G | A | 2 | a0004c0005t0002g0137a0004c0005t0002g0138 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1290+3954C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280858 | ||||||
| chr17:45280887
|
A | G | 11 | a0001c0001t0001g0258a0001c0001t0002g0256a0001c0002t0001g0023others(8): Show | 11 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1290+3925T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280887 | ||||||
| chr17:45280936
|
C | T | 2 | a0004c0005t0002g0137a0004c0005t0002g0138 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1290+3876G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280936 | ||||||
| chr17:45281051
|
T | C | 18 | a0001c0001t0002g0081a0001c0001t0003g0004a0001c0001t0003g0008others(15): Show | 21 | HG00408.hp1 HG00621.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1290+3761A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281051 | ||||||
| chr17:45281314
|
A | T | 1 | a0001c0001t0005g0155 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1290+3498T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281314 | ||||||
| chr17:45281324
|
G | A | 1 | a0001c0001t0002g0249 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1290+3488C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281324 | ||||||
| chr17:45281504
|
G | C | 1 | a0001c0002t0001g0116 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1290+3308C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281504 | ||||||
| chr17:45281640
|
C | CT | 57 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0061others(54): Show | 57 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1290+3171dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281640 | ||||||
| chr17:45281640
|
C | CTT | 6 | a0001c0001t0001g0013a0001c0001t0001g0147a0001c0001t0001g0172others(3): Show | 7 | HG02486.hp1 HG03516.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.1290+3170_1290+317 others(6): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281640 | ||||||
| chr17:45281640
|
CT | C | 8 | a0001c0001t0001g0160a0001c0001t0002g0130a0001c0001t0002g0250others(5): Show | 8 | HG00323.hp2 HG02004.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.1290+3171delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281640 | ||||||
| chr17:45281640
|
CTTT | C | 19 | a0001c0001t0002g0081a0001c0001t0003g0004a0001c0001t0003g0008others(16): Show | 22 | HG00408.hp1 HG00621.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.1290+3169_1290+317 others(7): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281640 | ||||||
| chr17:45281671
|
G | A | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG03209.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1290+3141C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281671 | ||||||
| chr17:45281731
|
G | A | 1 | a0001c0001t0010g0279 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1290+3081C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281731 | ||||||
| chr17:45281758
|
C | G | 1 | a0001c0001t0001g0021 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1290+3054G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281758 | ||||||
| chr17:45281874
|
A | G | 260 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(257): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1290+2938T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281874 | ||||||
| chr17:45281933
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1290+2879G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281933 | ||||||
| chr17:45282105
|
T | G | 1 | a0001c0002t0001g0039 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1290+2707A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282105 | ||||||
| chr17:45282217
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1290+2595C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282217 | ||||||
| chr17:45282465
|
G | C | 1 | a0001c0009t0001g0219 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1290+2347C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282465 | ||||||
| chr17:45282524
|
T | C | 147 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(144): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1290+2288A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282524 | ||||||
| chr17:45282538
|
G | C | 3 | a0001c0001t0002g0192a0001c0001t0002g0210a0001c0001t0002g0218 | 3 | HG01109.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1290+2274C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282538 | ||||||
| chr17:45282554
|
C | CA | 109 | a0001c0001t0001g0022a0001c0001t0001g0200a0001c0001t0001g0201others(106): Show | 135 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1290+2257dupT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282554 | ||||||
| chr17:45282554
|
CA | C | 144 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(141): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1290+2257delT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282554 | ||||||
| chr17:45282559
|
A | G | 1 | a0002c0003t0001g0224 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1290+2253T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282559 | ||||||
| chr17:45282690
|
G | A | 113 | a0001c0001t0001g0022a0001c0001t0001g0200a0001c0001t0001g0201others(110): Show | 140 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1290+2122C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282690 | ||||||
| chr17:45282753
|
C | T | 6 | a0001c0001t0001g0234a0001c0001t0002g0016a0001c0001t0002g0188others(3): Show | 7 | HG01884.hp2 HG02109.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1290+2059G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282753 | ||||||
| chr17:45282761
|
A | G | 260 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(257): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1290+2051T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282761 | ||||||
| chr17:45282881
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1290+1931G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282881 | ||||||
| chr17:45282971
|
GGCAGCTC others(15): Show |
G | 1 | a0001c0001t0001g0067 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1290+1819_1290+184 others(26): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282971 | ||||||
| chr17:45283260
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1290+1552G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283260 | ||||||
| chr17:45283340
|
C | T | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1290+1472G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283340 | ||||||
| chr17:45283463
|
A | G | 2 | a0001c0001t0002g0275a0001c0001t0015g0189 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1290+1349T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283463 | ||||||
| chr17:45283573
|
G | T | 38 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0001t0003g0042others(35): Show | 42 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1290+1239C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283573 | ||||||
| chr17:45283627
|
G | A | 74 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0064others(71): Show | 75 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1290+1185C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283627 | ||||||
| chr17:45283846
|
G | A | 41 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0142others(38): Show | 42 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.1290+966C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283846 | ||||||
| chr17:45283880
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1290+932C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283880 | ||||||
| chr17:45283931
|
G | A | 2 | a0001c0001t0005g0143a0001c0001t0005g0171 | 2 | HG00140.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1290+881C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283931 | ||||||
| chr17:45283983
|
C | G | 260 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(257): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1290+829G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283983 | ||||||
| chr17:45284124
|
G | A | 112 | a0001c0001t0001g0022a0001c0001t0001g0200a0001c0001t0001g0201others(109): Show | 139 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1290+688C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45284124 | ||||||
| chr17:45284421
|
C | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0004c0005t0002g0137others(1): Show | 4 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1290+391G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45284421 | ||||||
| chr17:45284522
|
C | A | 112 | a0001c0001t0001g0022a0001c0001t0001g0200a0001c0001t0001g0201others(109): Show | 139 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1290+290G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45284522 | ||||||
| chr17:45285050
|
G | A | 1 | a0001c0001t0002g0285 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1153-101C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285050 | ||||||
| chr17:45285089
|
C | T | 7 | a0001c0001t0002g0071a0001c0001t0002g0077a0001c0001t0002g0088others(4): Show | 7 | HG00558.hp1 HG02080.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.1153-140G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285089 | ||||||
| chr17:45285108
|
C | T | 58 | a0001c0001t0001g0022a0001c0001t0001g0064a0001c0001t0001g0065others(55): Show | 62 | HG01109.hp2 HG01243.hp2 HG01358.hp1 others(59): Show |
intron_variant | MODIFIER | c.1153-159G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285108 | ||||||
| chr17:45285127
|
G | A | 1 | a0001c0001t0002g0149 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1153-178C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285127 | ||||||
| chr17:45285148
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1153-199G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285148 | ||||||
| chr17:45285554
|
A | G | 9 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(6): Show | 9 | HG02145.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1153-605T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285554 | ||||||
| chr17:45285579
|
T | C | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1153-630A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285579 | ||||||
| chr17:45285632
|
A | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0001g0180 | 3 | HG01256.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1153-683T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285632 | ||||||
| chr17:45285705
|
G | A | 1 | a0001c0001t0004g0290 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1152+726C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285705 | ||||||
| chr17:45285800
|
A | T | 15 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0257others(12): Show | 15 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1152+631T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285800 | ||||||
| chr17:45285967
|
TA | T | 46 | a0001c0001t0001g0022a0001c0001t0001g0064a0001c0001t0001g0065others(43): Show | 51 | HG00099.hp2 HG01109.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.1152+463delT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285967 | ||||||
| chr17:45286005
|
C | G | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0004c0005t0002g0137others(1): Show | 4 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+426G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45286005 | ||||||
| chr17:45286006
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1152+425G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45286006 | ||||||
| chr17:45286092
|
G | A | 1 | a0001c0001t0003g0104 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1152+339C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45286092 | ||||||
| chr17:45286337
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1152+94C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45286337 | ||||||
| chr17:45287111
|
G | A | 7 | a0001c0001t0004g0018a0001c0001t0004g0233a0001c0001t0004g0290others(4): Show | 8 | HG01891.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.537+43C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 4/15 | chr17 | 45287111 | ||||||
| chr17:45287127
|
G | A | 1 | a0001c0001t0002g0188 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.537+27C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 4/15 | chr17 | 45287127 | ||||||
| chr17:45287371
|
C | A | 16 | a0001c0001t0002g0081a0001c0001t0003g0004a0001c0001t0003g0008others(13): Show | 19 | HG00621.hp2 HG01069.hp2 HG01175.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.327-7G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287371 | ||||||
| chr17:45287399
|
C | T | 2 | a0001c0001t0003g0100a0001c0001t0003g0101 | 2 | NA18974.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.327-35G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287399 | ||||||
| chr17:45287407
|
C | T | 2 | a0001c0002t0001g0023a0001c0002t0001g0024 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.327-43G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287407 | ||||||
| chr17:45287474
|
G | T | 4 | a0001c0001t0001g0258a0001c0002t0001g0027a0001c0002t0001g0028others(1): Show | 4 | HG02257.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-110C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287474 | ||||||
| chr17:45287499
|
G | A | 9 | a0001c0001t0001g0257a0001c0001t0002g0256a0001c0001t0015g0189others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-135C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287499 | ||||||
| chr17:45287516
|
G | GA | 18 | a0001c0001t0002g0081a0001c0001t0002g0275a0001c0001t0003g0004others(15): Show | 21 | HG00621.hp2 HG01069.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.327-153dupT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287516 | ||||||
| chr17:45287548
|
A | G | 60 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0043others(57): Show | 65 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.327-184T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287548 | ||||||
| chr17:45287637
|
A | G | 2 | a0001c0001t0001g0264a0001c0002t0009g0265 | 2 | HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.327-273T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287637 | ||||||
| chr17:45287649
|
G | A | 18 | a0001c0001t0002g0081a0001c0001t0003g0004a0001c0001t0003g0008others(15): Show | 21 | HG00408.hp1 HG00621.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.327-285C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287649 | ||||||
| chr17:45287723
|
C | T | 50 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0142others(47): Show | 51 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.327-359G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287723 | ||||||
| chr17:45287818
|
G | A | 7 | a0001c0001t0005g0143a0001c0001t0005g0155a0001c0001t0005g0169others(4): Show | 7 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.327-454C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287818 | ||||||
| chr17:45287889
|
T | G | 1 | a0001c0001t0002g0096 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.327-525A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287889 | ||||||
| chr17:45287895
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.327-531C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287895 | ||||||
| chr17:45287964
|
C | T | 4 | a0001c0001t0001g0190a0001c0001t0001g0191a0004c0005t0002g0137others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-600G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287964 | ||||||
| chr17:45288026
|
G | A | 41 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0142others(38): Show | 42 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.327-662C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45288026 | ||||||
| chr17:45288075
|
A | G | 41 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0142others(38): Show | 42 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.327-711T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45288075 | ||||||
| chr17:45288360
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG01106.hp1 NA18960.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.326+876C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45288360 | ||||||
| chr17:45288379
|
G | GT | 170 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0043others(167): Show | 200 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.326+856dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45288379 | ||||||
| chr17:45288379
|
G | GTT | 48 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0142others(45): Show | 49 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.326+855_326+856dup others(2): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45288379 | ||||||
| chr17:45288597
|
C | T | 1 | a0001c0001t0002g0188 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.326+639G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45288597 | ||||||
| chr17:45289181
|
G | T | 23 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0002g0256others(20): Show | 25 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.326+55C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45289181 | ||||||
| chr17:45289336
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.257-31C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289336 | ||||||
| chr17:45289488
|
A | G | 2 | a0001c0001t0002g0275a0001c0001t0015g0189 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.257-183T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289488 | ||||||
| chr17:45289708
|
A | C | 1 | a0001c0002t0016g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.257-403T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289708 | ||||||
| chr17:45289786
|
G | A | 74 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0009others(71): Show | 97 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.257-481C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289786 | ||||||
| chr17:45289790
|
C | T | 1 | a0001c0002t0001g0211 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.257-485G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289790 | ||||||
| chr17:45289919
|
C | T | 1 | a0001c0001t0003g0102 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.256+571G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289919 | ||||||
| chr17:45289941
|
G | A | 1 | a0001c0001t0002g0133 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.256+549C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289941 | ||||||
| chr17:45289965
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.256+525A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289965 | ||||||
| chr17:45290058
|
C | T | 15 | a0001c0002t0001g0006a0001c0002t0001g0228a0001c0002t0001g0229others(12): Show | 17 | HG00140.hp1 HG00323.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.256+432G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45290058 | ||||||
| chr17:45290117
|
G | C | 1 | a0001c0002t0001g0054 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.256+373C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45290117 | ||||||
| chr17:45290287
|
T | C | 227 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(224): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.256+203A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45290287 | ||||||
| chr17:45290896
|
T | C | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0002t0001g0007others(5): Show | 9 | HG00099.hp1 HG00280.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20-131A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45290896 | ||||||
| chr17:45290949
|
C | T | 5 | a0001c0001t0007g0236a0001c0001t0007g0237a0001c0001t0007g0238others(2): Show | 5 | HG02486.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-184G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45290949 | ||||||
| chr17:45290951
|
C | A | 3 | a0001c0002t0001g0023a0001c0002t0001g0024a0003c0004t0001g0025 | 3 | HG01069.hp1 HG01071.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-20-186G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45290951 | ||||||
| chr17:45290973
|
C | T | 7 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0002g0256others(4): Show | 7 | HG01243.hp1 HG02257.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20-208G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45290973 | ||||||
| chr17:45291024
|
G | A | 1 | a0001c0002t0009g0265 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-20-259C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291024 | ||||||
| chr17:45291234
|
C | T | 5 | a0001c0002t0001g0005a0001c0002t0001g0209a0001c0002t0001g0221others(2): Show | 7 | HG00733.hp1 HG00735.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20-469G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291234 | ||||||
| chr17:45291296
|
C | CTG | 24 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0287others(21): Show | 26 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-20-533_-20-532dup others(2): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291296 | ||||||
| chr17:45291296
|
CTG | C | 204 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(201): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.-20-533_-20-532del others(2): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291296 | ||||||
| chr17:45291500
|
T | C | 2 | a0001c0001t0002g0275a0001c0001t0015g0189 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-20-735A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291500 | ||||||
| chr17:45291515
|
C | T | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG03209.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-20-750G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291515 | ||||||
| chr17:45291541
|
G | T | 5 | a0001c0001t0007g0236a0001c0001t0007g0237a0001c0001t0007g0238others(2): Show | 5 | HG02486.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-776C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291541 | ||||||
| chr17:45291561
|
C | T | 2 | a0004c0005t0002g0137a0004c0005t0002g0138 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-20-796G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291561 | ||||||
| chr17:45291820
|
G | A | 1 | a0001c0002t0001g0057 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-20-1055C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291820 | ||||||
| chr17:45292241
|
GGTGGCCT others(6): Show |
G | 46 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0064others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-20-1489_-20-1477d others(15): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292241 | ||||||
| chr17:45292286
|
C | T | 11 | a0001c0001t0001g0193a0001c0001t0001g0234a0001c0001t0001g0266others(8): Show | 12 | HG01243.hp2 HG01884.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-1521G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292286 | ||||||
| chr17:45292287
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-20-1522C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292287 | ||||||
| chr17:45292411
|
C | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-20-1646G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292411 | ||||||
| chr17:45292427
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0147a0001c0001t0001g0179 | 4 | NA18963.hp2 NA18964.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-1662C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292427 | ||||||
| chr17:45292538
|
G | C | 46 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0064others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-20-1773C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292538 | ||||||
| chr17:45292614
|
C | G | 5 | a0001c0002t0001g0005a0001c0002t0001g0209a0001c0002t0001g0221others(2): Show | 7 | HG00733.hp1 HG00735.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20-1849G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292614 | ||||||
| chr17:45292903
|
C | T | 2 | a0001c0001t0002g0086a0001c0001t0002g0117 | 2 | HG02027.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-20-2138G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292903 | ||||||
| chr17:45292938
|
G | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-20-2173C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292938 | ||||||
| chr17:45292993
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-20-2228C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292993 | ||||||
| chr17:45293115
|
C | T | 68 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(65): Show | 90 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.-20-2350G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293115 | ||||||
| chr17:45293172
|
C | T | 11 | a0001c0001t0001g0193a0001c0001t0001g0234a0001c0001t0001g0266others(8): Show | 12 | HG01243.hp2 HG01884.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-2407G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293172 | ||||||
| chr17:45293184
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-20-2419T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293184 | ||||||
| chr17:45293447
|
A | G | 2 | a0001c0001t0002g0275a0001c0001t0015g0189 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-20-2682T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293447 | ||||||
| chr17:45293846
|
G | T | 1 | a0001c0001t0015g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20-3081C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293846 | ||||||
| chr17:45293847
|
A | G | 1 | a0001c0001t0015g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20-3082T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293847 | ||||||
| chr17:45293908
|
G | A | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-3143C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293908 | ||||||
| chr17:45293929
|
G | T | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0200others(15): Show | 18 | HG01099.hp1 HG02145.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-20-3164C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293929 | ||||||
| chr17:45294251
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-20-3486C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45294251 | ||||||
| chr17:45294263
|
G | A | 1 | a0001c0001t0003g0072 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-20-3498C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45294263 | ||||||
| chr17:45294479
|
C | T | 1 | a0001c0001t0008g0199 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-20-3714G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45294479 | ||||||
| chr17:45294521
|
T | C | 5 | a0001c0001t0007g0236a0001c0001t0007g0237a0001c0001t0007g0238others(2): Show | 5 | HG02486.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-3756A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45294521 | ||||||
| chr17:45295156
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-20-4391A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45295156 | ||||||
| chr17:45295202
|
C | T | 10 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0002g0256others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20-4437G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45295202 | ||||||
| chr17:45295223
|
A | AT | 160 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(157): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-20-4459dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45295223 | ||||||
| chr17:45295496
|
T | C | 1 | a0001c0002t0001g0058 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-20-4731A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45295496 | ||||||
| chr17:45295766
|
A | T | 1 | a0001c0002t0001g0045 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-20-5001T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45295766 | ||||||
| chr17:45296034
|
C | T | 10 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0002g0256others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20-5269G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296034 | ||||||
| chr17:45296089
|
G | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0003g0073 | 3 | HG01099.hp1 HG01175.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-20-5324C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296089 | ||||||
| chr17:45296179
|
C | T | 1 | a0001c0001t0007g0236 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-20-5414G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296179 | ||||||
| chr17:45296262
|
C | T | 1 | a0001c0001t0015g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20-5497G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296262 | ||||||
| chr17:45296396
|
A | G | 11 | a0001c0001t0001g0193a0001c0001t0001g0234a0001c0001t0001g0266others(8): Show | 12 | HG01243.hp2 HG01884.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-5631T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296396 | ||||||
| chr17:45296410
|
A | G | 2 | a0001c0001t0003g0100a0001c0001t0003g0101 | 2 | NA18974.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-20-5645T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296410 | ||||||
| chr17:45296689
|
T | C | 37 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0001t0002g0051others(34): Show | 41 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.-20-5924A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296689 | ||||||
| chr17:45296737
|
A | T | 11 | a0001c0001t0001g0193a0001c0001t0001g0234a0001c0001t0001g0266others(8): Show | 12 | HG01243.hp2 HG01884.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-5972T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296737 | ||||||
| chr17:45296812
|
C | T | 2 | a0001c0001t0003g0100a0001c0001t0003g0101 | 2 | NA18974.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-20-6047G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296812 | ||||||
| chr17:45297286
|
A | G | 1 | a0001c0001t0002g0248 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-20-6521T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297286 | ||||||
| chr17:45297357
|
G | A | 11 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0233others(8): Show | 13 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20-6592C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297357 | ||||||
| chr17:45297436
|
C | T | 1 | a0001c0001t0015g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20-6671G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297436 | ||||||
| chr17:45297494
|
G | A | 2 | a0001c0001t0002g0095a0001c0001t0002g0096 | 2 | HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.-20-6729C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297494 | ||||||
| chr17:45297572
|
A | T | 1 | a0001c0001t0002g0085 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-20-6807T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297572 | ||||||
| chr17:45297716
|
C | CT | 12 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0002g0256others(9): Show | 12 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-6952dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297716 | ||||||
| chr17:45297716
|
CT | C | 163 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0064others(160): Show | 191 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.-20-6952delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297716 | ||||||
| chr17:45297716
|
CTT | C | 37 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0001t0002g0051others(34): Show | 41 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.-20-6953_-20-6952d others(4): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297716 | ||||||
| chr17:45297746
|
G | A | 14 | a0001c0001t0001g0013a0001c0001t0001g0145a0001c0001t0001g0147others(11): Show | 15 | HG00735.hp1 HG00741.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20-6981C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297746 | ||||||
| chr17:45297814
|
G | A | 5 | a0001c0001t0007g0236a0001c0001t0007g0237a0001c0001t0007g0238others(2): Show | 5 | HG02486.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-7049C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297814 | ||||||
| chr17:45297873
|
C | T | 36 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0001t0002g0051others(33): Show | 40 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-20-7108G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297873 | ||||||
| chr17:45297987
|
G | A | 2 | a0001c0001t0002g0275a0001c0001t0004g0276 | 2 | HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20-7222C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297987 | ||||||
| chr17:45298128
|
C | A | 1 | a0001c0001t0002g0098 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-20-7363G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298128 | ||||||
| chr17:45298202
|
C | T | 1 | a0001c0002t0016g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-20-7437G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298202 | ||||||
| chr17:45298744
|
C | T | 80 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(77): Show | 86 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.-20-7979G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298744 | ||||||
| chr17:45298777
|
G | C | 12 | a0001c0001t0001g0287a0001c0001t0004g0018a0001c0001t0004g0019others(9): Show | 14 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-20-8012C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298777 | ||||||
| chr17:45298817
|
C | G | 11 | a0001c0001t0001g0193a0001c0001t0001g0234a0001c0001t0001g0266others(8): Show | 12 | HG01243.hp2 HG01884.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-8052G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298817 | ||||||
| chr17:45298829
|
C | T | 2 | a0001c0001t0002g0111a0001c0001t0002g0136 | 2 | HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-20-8064G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298829 | ||||||
| chr17:45298833
|
A | G | 1 | a0001c0001t0004g0019 | 2 | HG01358.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-20-8068T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298833 | ||||||
| chr17:45298848
|
A | T | 1 | a0001c0002t0001g0116 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-20-8083T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298848 | ||||||
| chr17:45299032
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-20-8267T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299032 | ||||||
| chr17:45299062
|
C | T | 1 | a0001c0001t0002g0208 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-20-8297G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299062 | ||||||
| chr17:45299075
|
G | GTA | 5 | a0001c0001t0007g0236a0001c0001t0007g0237a0001c0001t0007g0238others(2): Show | 5 | HG02486.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-8312_-20-8311d others(4): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299075 | ||||||
| chr17:45299081
|
C | T | 117 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(114): Show | 143 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.-20-8316G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299081 | ||||||
| chr17:45299140
|
G | A | 1 | a0001c0002t0001g0229 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-20-8375C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299140 | ||||||
| chr17:45299180
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-20-8415C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299180 | ||||||
| chr17:45299244
|
A | G | 1 | a0001c0001t0004g0288 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-20-8479T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299244 | ||||||
| chr17:45299395
|
T | G | 118 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(115): Show | 144 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.-20-8630A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299395 | ||||||
| chr17:45299595
|
C | T | 1 | a0001c0001t0002g0115 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-20-8830G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299595 | ||||||
| chr17:45299954
|
G | A | 40 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0142others(37): Show | 41 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-20-9189C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299954 | ||||||
| chr17:45300138
|
G | T | 4 | a0001c0001t0001g0258a0001c0002t0001g0027a0001c0002t0001g0028others(1): Show | 4 | HG02257.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-9373C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300138 | ||||||
| chr17:45300153
|
T | A | 1 | a0001c0002t0001g0230 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-20-9388A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300153 | ||||||
| chr17:45300185
|
CA | C | 40 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0142others(37): Show | 41 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-20-9421delT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300185 | ||||||
| chr17:45300224
|
C | T | 1 | a0001c0002t0001g0240 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-20-9459G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300224 | ||||||
| chr17:45300267
|
T | C | 1 | a0001c0002t0001g0295 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-20-9502A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300267 | ||||||
| chr17:45300357
|
TC | T | 11 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0002g0256others(8): Show | 11 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20-9593delG | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300357 | ||||||
| chr17:45300801
|
T | C | 1 | a0001c0002t0001g0295 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-20-10036A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300801 | ||||||
| chr17:45300846
|
T | TA | 116 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(113): Show | 142 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-10082_-20-1008 others(5): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300846 | ||||||
| chr17:45300847
|
T | A | 182 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0064others(179): Show | 211 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.-20-10082A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300847 | ||||||
| chr17:45301032
|
G | C | 40 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0142others(37): Show | 41 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-20-10267C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45301032 | ||||||
| chr17:45301124
|
C | T | 3 | a0001c0001t0001g0278a0001c0001t0001g0281a0001c0008t0002g0277 | 3 | HG02572.hp1 HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-20-10359G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45301124 | ||||||
| chr17:45301167
|
C | CA | 18 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0002g0011others(15): Show | 19 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-20-10403dupT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45301167 | ||||||
| chr17:45301271
|
C | T | 2 | a0001c0002t0001g0196a0005c0007t0002g0197 | 2 | NA19065.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-20-10506G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45301271 | ||||||
| chr17:45301335
|
T | C | 2 | a0001c0001t0002g0248a0001c0001t0002g0251 | 2 | HG00642.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.-20-10570A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45301335 | ||||||
| chr17:45301687
|
A | G | 1 | a0001c0001t0002g0113 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-20-10922T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45301687 | ||||||
| chr17:45301833
|
CT | C | 68 | a0001c0001t0001g0161a0001c0001t0001g0193a0001c0001t0001g0234others(65): Show | 74 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.-20-11069delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45301833 | ||||||
| chr17:45302101
|
C | G | 295 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(292): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-20-11336G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302101 | ||||||
| chr17:45302122
|
C | T | 40 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0142others(37): Show | 41 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-20-11357G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302122 | ||||||
| chr17:45302167
|
GT | G | 115 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(112): Show | 141 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.-20-11403delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302167 | ||||||
| chr17:45302221
|
C | T | 8 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(5): Show | 8 | HG02145.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20-11456G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302221 | ||||||
| chr17:45302383
|
C | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0002t0001g0044 | 3 | NA19058.hp1 NA19074.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-20-11618G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302383 | ||||||
| chr17:45302399
|
T | C | 40 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0142others(37): Show | 41 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-20-11634A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302399 | ||||||
| chr17:45302697
|
T | C | 1 | a0001c0002t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-20-11932A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302697 | ||||||
| chr17:45302749
|
C | T | 40 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0142others(37): Show | 41 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-20-11984G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302749 | ||||||
| chr17:45302851
|
C | CT | 295 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(292): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-20-12087_-20-1208 others(5): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302851 | ||||||
| chr17:45302854
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-20-12089T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302854 | ||||||
| chr17:45302975
|
G | A | 40 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0142others(37): Show | 41 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-20-12210C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302975 | ||||||
| chr17:45303300
|
A | C | 216 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0043others(213): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-20-12535T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303300 | ||||||
| chr17:45303326
|
C | T | 11 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0002g0256others(8): Show | 11 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20-12561G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303326 | ||||||
| chr17:45303443
|
C | T | 13 | a0001c0001t0001g0193a0001c0001t0001g0234a0001c0001t0001g0266others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-20-12678G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303443 | ||||||
| chr17:45303465
|
G | A | 1 | a0001c0001t0004g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-20-12700C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303465 | ||||||
| chr17:45303741
|
C | CT | 15 | a0001c0001t0001g0142a0001c0001t0001g0259a0001c0001t0001g0260others(12): Show | 15 | HG02145.hp1 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20-12977dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303741 | ||||||
| chr17:45303817
|
C | T | 2 | a0001c0001t0007g0237a0001c0001t0007g0238 | 2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-20-13052G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303817 | ||||||
| chr17:45303867
|
C | T | 7 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0002g0256others(4): Show | 7 | HG01243.hp1 HG02257.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21+13093G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303867 | ||||||
| chr17:45303884
|
G | A | 3 | a0001c0001t0002g0275a0001c0001t0004g0276a0001c0001t0015g0189 | 3 | HG02615.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-21+13076C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303884 | ||||||
| chr17:45303935
|
C | T | 1 | a0001c0001t0008g0199 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-21+13025G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303935 | ||||||
| chr17:45304010
|
C | CT | 38 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0001t0001g0151others(35): Show | 42 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.-21+12949dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45304010 | ||||||
| chr17:45304010
|
CT | C | 21 | a0001c0001t0001g0180a0001c0001t0002g0099a0001c0001t0002g0135others(18): Show | 23 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.-21+12949delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45304010 | ||||||
| chr17:45304015
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-21+12945A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45304015 | ||||||
| chr17:45304105
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-21+12855G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45304105 | ||||||
| chr17:45304106
|
G | A | 19 | a0001c0001t0002g0081a0001c0001t0002g0110a0001c0001t0003g0004others(16): Show | 22 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.-21+12854C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45304106 | ||||||
| chr17:45304193
|
G | A | 2 | a0001c0001t0002g0111a0001c0001t0002g0136 | 2 | HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-21+12767C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45304193 | ||||||
| chr17:45304642
|
G | A | 12 | a0001c0001t0001g0287a0001c0001t0004g0018a0001c0001t0004g0019others(9): Show | 14 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21+12318C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45304642 | ||||||
| chr17:45305010
|
C | A | 1 | a0001c0002t0001g0058 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-21+11950G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305010 | ||||||
| chr17:45305125
|
T | A | 1 | a0001c0001t0004g0294 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-21+11835A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305125 | ||||||
| chr17:45305136
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-21+11824G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305136 | ||||||
| chr17:45305396
|
G | GT | 123 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0064others(120): Show | 139 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-21+11563dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305396 | ||||||
| chr17:45305396
|
G | GTT | 19 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 19 | HG01175.hp2 HG01243.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-21+11562_-21+1156 others(6): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305396 | ||||||
| chr17:45305498
|
C | T | 1 | a0001c0001t0002g0079 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-21+11462G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305498 | ||||||
| chr17:45305569
|
T | A | 13 | a0001c0001t0001g0193a0001c0001t0001g0234a0001c0001t0001g0266others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21+11391A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305569 | ||||||
| chr17:45305734
|
A | G | 182 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0064others(179): Show | 211 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.-21+11226T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305734 | ||||||
| chr17:45306073
|
A | C | 1 | a0001c0002t0001g0295 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-21+10887T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306073 | ||||||
| chr17:45306118
|
G | A | 217 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0043others(214): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.-21+10842C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306118 | ||||||
| chr17:45306158
|
G | A | 11 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0002g0256others(8): Show | 11 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21+10802C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306158 | ||||||
| chr17:45306229
|
C | T | 40 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0142others(37): Show | 41 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-21+10731G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306229 | ||||||
| chr17:45306230
|
A | G | 182 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0064others(179): Show | 211 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.-21+10730T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306230 | ||||||
| chr17:45306333
|
T | TAAAAATT others(251): Show |
2 | a0001c0002t0001g0027a0001c0002t0001g0028 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-21+10626_-21+1062 others(262): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306333 | ||||||
| chr17:45306333
|
T | TAAAAATT others(252): Show |
1 | a0001c0002t0001g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-21+10626_-21+1062 others(263): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306333 | ||||||
| chr17:45306333
|
T | TAAAAATT others(265): Show |
1 | a0001c0002t0001g0023 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-21+10626_-21+1062 others(276): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306333 | ||||||
| chr17:45306333
|
T | TAAAAATT others(266): Show |
2 | a0001c0002t0001g0024a0003c0004t0001g0025 | 2 | HG01071.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-21+10626_-21+1062 others(277): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306333 | ||||||
| chr17:45306333
|
T | TAAAAATT others(273): Show |
2 | a0001c0001t0002g0256a0001c0010t0009g0255 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-21+10626_-21+1062 others(284): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306333 | ||||||
| chr17:45306333
|
T | TAAAAATT others(274): Show |
1 | a0001c0001t0001g0257 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-21+10626_-21+1062 others(285): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306333 | ||||||
| chr17:45306333
|
T | TAAAAATT others(275): Show |
1 | a0001c0001t0001g0258 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-21+10626_-21+1062 others(286): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306333 | ||||||
| chr17:45306696
|
T | C | 1 | a0001c0001t0002g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-21+10264A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306696 | ||||||
| chr17:45306874
|
C | G | 13 | a0001c0001t0001g0287a0001c0001t0004g0018a0001c0001t0004g0019others(10): Show | 15 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-21+10086G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306874 | ||||||
| chr17:45306906
|
A | C | 1 | a0001c0001t0002g0140 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-21+10054T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306906 | ||||||
| chr17:45306907
|
C | A | 1 | a0001c0001t0002g0140 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-21+10053G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306907 | ||||||
| chr17:45306979
|
C | T | 36 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0001t0002g0051others(33): Show | 40 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-21+9981G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306979 | ||||||
| chr17:45307073
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-21+9887G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45307073 | ||||||
| chr17:45307199
|
A | C | 1 | a0001c0001t0002g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-21+9761T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45307199 | ||||||
| chr17:45307266
|
A | T | 111 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(108): Show | 137 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.-21+9694T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45307266 | ||||||
| chr17:45307564
|
T | C | 1 | a0003c0004t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-21+9396A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45307564 | ||||||
| chr17:45307720
|
C | T | 13 | a0001c0001t0001g0287a0001c0001t0004g0018a0001c0001t0004g0019others(10): Show | 15 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-21+9240G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45307720 | ||||||
| chr17:45307897
|
C | A | 40 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0142others(37): Show | 41 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-21+9063G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45307897 | ||||||
| chr17:45307983
|
G | A | 165 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0064others(162): Show | 192 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.-21+8977C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45307983 | ||||||
| chr17:45308109
|
T | C | 2 | a0001c0001t0002g0016a0001c0001t0002g0235 | 3 | HG01243.hp2 HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-21+8851A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308109 | ||||||
| chr17:45308148
|
G | A | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG03209.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-21+8812C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308148 | ||||||
| chr17:45308254
|
G | T | 40 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0142others(37): Show | 41 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-21+8706C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308254 | ||||||
| chr17:45308487
|
T | G | 1 | a0001c0001t0002g0141 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-21+8473A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308487 | ||||||
| chr17:45308563
|
G | A | 3 | a0001c0002t0001g0023a0001c0002t0001g0024a0003c0004t0001g0025 | 3 | HG01069.hp1 HG01071.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-21+8397C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308563 | ||||||
| chr17:45308569
|
C | T | 1 | a0001c0001t0002g0077 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-21+8391G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308569 | ||||||
| chr17:45308671
|
CT | C | 12 | a0001c0001t0001g0193a0001c0001t0001g0234a0001c0001t0001g0266others(9): Show | 13 | HG01169.hp1 HG01243.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-21+8288delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308671 | ||||||
| chr17:45308744
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-21+8216A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308744 | ||||||
| chr17:45308792
|
C | T | 1 | a0001c0001t0002g0076 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-21+8168G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308792 | ||||||
| chr17:45308793
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-21+8167C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308793 | ||||||
| chr17:45308958
|
C | T | 2 | a0001c0002t0001g0031a0001c0002t0001g0032 | 2 | HG02040.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.-21+8002G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308958 | ||||||
| chr17:45308988
|
AT | A | 180 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0064others(177): Show | 209 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.-21+7971delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308988 | ||||||
| chr17:45309021
|
T | G | 3 | a0001c0001t0002g0275a0001c0001t0004g0276a0001c0001t0015g0189 | 3 | HG02615.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-21+7939A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309021 | ||||||
| chr17:45309175
|
C | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0002t0016g0150 | 3 | HG03041.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-21+7785G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309175 | ||||||
| chr17:45309232
|
G | A | 1 | a0001c0002t0016g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-21+7728C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309232 | ||||||
| chr17:45309257
|
T | C | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0002t0016g0150 | 3 | HG03041.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-21+7703A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309257 | ||||||
| chr17:45309343
|
C | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0002g0186others(2): Show | 5 | HG01099.hp1 HG01175.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+7617G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309343 | ||||||
| chr17:45309361
|
C | A | 1 | a0001c0002t0001g0274 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-21+7599G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309361 | ||||||
| chr17:45309738
|
T | G | 181 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(178): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.-21+7222A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309738 | ||||||
| chr17:45309807
|
C | T | 1 | a0001c0001t0008g0199 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-21+7153G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309807 | ||||||
| chr17:45309878
|
A | C | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0015g0189 | 3 | HG02886.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-21+7082T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309878 | ||||||
| chr17:45310027
|
C | CT | 11 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0282others(8): Show | 11 | HG01243.hp1 HG01261.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21+6932dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310027 | ||||||
| chr17:45310027
|
C | CTT | 7 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0269others(4): Show | 7 | HG02622.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-21+6931_-21+6932d others(4): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310027 | ||||||
| chr17:45310027
|
CT | C | 61 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0061others(58): Show | 64 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.-21+6932delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310027 | ||||||
| chr17:45310065
|
G | A | 1 | a0001c0001t0003g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-21+6895C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310065 | ||||||
| chr17:45310071
|
G | C | 1 | a0001c0002t0001g0242 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-21+6889C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310071 | ||||||
| chr17:45310074
|
G | A | 7 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0269others(4): Show | 7 | HG02622.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-21+6886C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310074 | ||||||
| chr17:45310091
|
A | T | 10 | a0001c0001t0001g0287a0001c0001t0004g0018a0001c0001t0004g0288others(7): Show | 11 | HG01891.hp1 HG02280.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21+6869T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310091 | ||||||
| chr17:45310369
|
T | C | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG03209.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-21+6591A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310369 | ||||||
| chr17:45310515
|
T | A | 1 | a0001c0001t0003g0182 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-21+6445A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310515 | ||||||
| chr17:45310521
|
C | T | 8 | a0001c0002t0001g0014a0001c0002t0001g0194a0001c0002t0001g0195others(5): Show | 9 | HG00673.hp1 HG02083.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21+6439G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310521 | ||||||
| chr17:45310623
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0002g0192 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-21+6337G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310623 | ||||||
| chr17:45311023
|
T | C | 4 | a0001c0002t0001g0243a0001c0002t0001g0244a0001c0002t0001g0245others(1): Show | 4 | HG02523.hp2 NA18948.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+5937A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45311023 | ||||||
| chr17:45311047
|
G | A | 9 | a0001c0001t0002g0017a0001c0001t0002g0247a0001c0001t0002g0248others(6): Show | 10 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.-21+5913C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45311047 | ||||||
| chr17:45311078
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-21+5882A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45311078 | ||||||
| chr17:45311258
|
T | C | 2 | a0001c0001t0005g0183a0001c0001t0005g0184 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-21+5702A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45311258 | ||||||
| chr17:45311494
|
G | A | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21+5466C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45311494 | ||||||
| chr17:45312126
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-21+4834C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45312126 | ||||||
| chr17:45312171
|
A | T | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-21+4789T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45312171 | ||||||
| chr17:45312360
|
T | A | 83 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(80): Show | 91 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-21+4600A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45312360 | ||||||
| chr17:45312514
|
A | G | 1 | a0001c0001t0003g0073 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-21+4446T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45312514 | ||||||
| chr17:45312636
|
G | T | 1 | a0001c0001t0003g0072 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-21+4324C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45312636 | ||||||
| chr17:45312755
|
G | A | 36 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0001t0002g0051others(33): Show | 40 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-21+4205C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45312755 | ||||||
| chr17:45312977
|
G | A | 48 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0001t0001g0287others(45): Show | 54 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-21+3983C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45312977 | ||||||
| chr17:45313013
|
G | A | 10 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0002g0256others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21+3947C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313013 | ||||||
| chr17:45313022
|
G | T | 1 | a0001c0001t0002g0071 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-21+3938C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313022 | ||||||
| chr17:45313118
|
C | T | 1 | a0001c0002t0001g0070 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-21+3842G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313118 | ||||||
| chr17:45313245
|
G | A | 2 | a0001c0001t0002g0275a0001c0001t0004g0276 | 2 | HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-21+3715C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313245 | ||||||
| chr17:45313252
|
T | C | 12 | a0001c0001t0001g0287a0001c0001t0004g0018a0001c0001t0004g0019others(9): Show | 14 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21+3708A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313252 | ||||||
| chr17:45313323
|
A | C | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21+3637T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313323 | ||||||
| chr17:45313397
|
A | G | 48 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0001t0001g0287others(45): Show | 54 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-21+3563T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313397 | ||||||
| chr17:45313431
|
A | G | 1 | a0001c0001t0002g0188 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-21+3529T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313431 | ||||||
| chr17:45313962
|
G | T | 48 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0001t0001g0287others(45): Show | 54 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-21+2998C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313962 | ||||||
| chr17:45314116
|
A | G | 7 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0002g0256others(4): Show | 7 | HG01243.hp1 HG02257.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21+2844T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45314116 | ||||||
| chr17:45314173
|
A | G | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-21+2787T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45314173 | ||||||
| chr17:45314229
|
C | T | 12 | a0001c0001t0001g0287a0001c0001t0004g0018a0001c0001t0004g0019others(9): Show | 14 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21+2731G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45314229 | ||||||
| chr17:45314379
|
T | G | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0002t0001g0273 | 3 | HG02622.hp1 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-21+2581A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45314379 | ||||||
| chr17:45314456
|
A | G | 10 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0002g0256others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21+2504T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45314456 | ||||||
| chr17:45314842
|
G | A | 87 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 95 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-21+2118C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45314842 | ||||||
| chr17:45314905
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-21+2055G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45314905 | ||||||
| chr17:45315015
|
C | CA | 40 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(37): Show | 42 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.-21+1944dupT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45315015 | ||||||
| chr17:45315278
|
A | G | 3 | a0001c0002t0001g0023a0001c0002t0001g0024a0003c0004t0001g0025 | 3 | HG01069.hp1 HG01071.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-21+1682T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45315278 | ||||||
| chr17:45316050
|
G | A | 5 | a0001c0001t0001g0278a0001c0001t0001g0281a0001c0001t0010g0279others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21+910C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316050 | ||||||
| chr17:45316172
|
G | A | 1 | a0001c0001t0004g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-21+788C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316172 | ||||||
| chr17:45316177
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-21+783G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316177 | ||||||
| chr17:45316201
|
G | A | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG02145.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-21+759C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316201 | ||||||
| chr17:45316344
|
T | C | 1 | a0001c0001t0002g0285 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-21+616A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316344 | ||||||
| chr17:45316651
|
G | A | 1 | a0001c0001t0002g0286 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-21+309C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316651 | ||||||
| chr17:45316697
|
C | A | 12 | a0001c0001t0001g0287a0001c0001t0004g0018a0001c0001t0004g0019others(9): Show | 14 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21+263G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316697 | ||||||
| chr17:45316702
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-21+258G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316702 | ||||||
| chr17:45316746
|
G | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-21+214C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316746 |