Search by Gene
| geneid | 11183 |
|---|---|
| ensemblid | ENSG00000012983.12 |
| hgncid | 6867 |
| symbol | MAP4K5 |
| name | mitogen-activated protein kinase kinase kinase kinase 5 |
| refseq_nuc | NM_006575.6 |
| refseq_prot | NP_006566.2 |
| ensembl_nuc | ENST00000682126.1 |
| ensembl_prot | ENSP00000507200.1 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 50418521 |
| end | 50532569 |
| strand | - |
| ver | v1.2 |
| region | chr14:50418521-50532569 |
| region5000 | chr14:50413521-50537569 |
| regionname0 | MAP4K5_chr14_50418521_50532569 |
| regionname5000 | MAP4K5_chr14_50413521_50537569 |
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 | 1/0 | 846 | 222 | 78 | 50 | 76 | 3 | 14 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0002 | 0/0 | 846 | 8 | 0 | 5 | 1 | 1 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0003 | 0/0 | 846 | 3 | 0 | 0 | 3 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0004 | 0/1 | 846 | 3 | 1 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0005 | 0/0 | 846 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0006 | 0/0 | 846 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0007 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | 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 | 1/0 | 2541 | 197 | 64 | 41 | 74 | 3 | 14 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0002 | 0/0 | 2541 | 8 | 0 | 5 | 1 | 1 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0003 | 0/0 | 2541 | 5 | 5 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0004 | 0/0 | 2541 | 4 | 0 | 4 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0005 | 0/0 | 2541 | 4 | 0 | 4 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0006 | 0/0 | 2541 | 4 | 4 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0007 | 0/0 | 2541 | 3 | 3 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0008 | 0/1 | 2541 | 3 | 1 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0009 | 0/0 | 2541 | 3 | 0 | 0 | 3 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0010 | 0/0 | 2541 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0011 | 0/0 | 2541 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0012 | 0/0 | 2541 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0013 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0014 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0015 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0016 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| c0017 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | 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 | 1730 | 199 | 78 | 48 | 57 | 3 | 11 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| t0002 | 0/0 | 1730 | 16 | 0 | 7 | 5 | 1 | 3 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| t0003 | 0/0 | 1730 | 14 | 0 | 0 | 14 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| t0004 | 0/0 | 1728 | 2 | 0 | 0 | 0 | 0 | 2 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| t0005 | 0/0 | 1730 | 2 | 0 | 0 | 2 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| t0006 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| t0007 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| t0008 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| t0009 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| t0010 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| t0011 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| t0012 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | 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 | 3 | 3 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0039 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0229 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| 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 | 1/0 | 197 | 64 | 41 | 74 | 3 | 14 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0007 | a0001 | c0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0012 | a0001 | c0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0013 | a0001 | c0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0014 | a0001 | c0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0015 | a0001 | c0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0017 | a0001 | c0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 8 | 0 | 5 | 1 | 1 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0003c0009 | a0003 | c0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0004c0008 | a0004 | c0008 | 0/1 | 3 | 1 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0005c0010 | a0005 | c0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0006c0011 | a0006 | c0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0007c0016 | a0007 | c0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | 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 | 1/0 | 160 | 63 | 34 | 51 | 2 | 9 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 16 | 0 | 7 | 5 | 1 | 3 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0004t0001 | a0001 | c0004 | t0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0005t0001 | a0001 | c0005 | t0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0006t0001 | a0001 | c0006 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0006t0010 | a0001 | c0006 | t0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0007t0001 | a0001 | c0007 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0012t0001 | a0001 | c0012 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0013t0001 | a0001 | c0013 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0014t0001 | a0001 | c0014 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0015t0008 | a0001 | c0015 | t0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0001c0017t0001 | a0001 | c0017 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0002c0002t0001 | a0002 | c0002 | t0001 | 0/0 | 7 | 0 | 4 | 1 | 1 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0002c0002t0007 | a0002 | c0002 | t0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0003c0009t0001 | a0003 | c0009 | t0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0004c0008t0001 | a0004 | c0008 | t0001 | 0/1 | 3 | 1 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0005c0010t0001 | a0005 | c0010 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0006c0011t0001 | a0006 | c0011 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | copy fasta |
| a0007c0016t0011 | a0007 | c0016 | t0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0181 | a0001 | c0001 | t0001 | g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0185 | a0001 | c0001 | t0001 | g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0187 | a0001 | c0001 | t0001 | g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0192 | a0001 | c0001 | t0001 | g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0198 | a0001 | c0001 | t0001 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0206 | a0001 | c0001 | t0001 | g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0207 | a0001 | c0001 | t0001 | g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0211 | a0001 | c0001 | t0001 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0212 | a0001 | c0001 | t0001 | g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0213 | a0001 | c0001 | t0001 | g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0214 | a0001 | c0001 | t0001 | g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0223 | a0001 | c0001 | t0001 | g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0224 | a0001 | c0001 | t0001 | g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0225 | a0001 | c0001 | t0001 | g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0226 | a0001 | c0001 | t0001 | g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0227 | a0001 | c0001 | t0001 | g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0228 | a0001 | c0001 | t0001 | g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0229 | a0001 | c0001 | t0001 | g0229 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0001g0230 | a0001 | c0001 | t0001 | g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0007 | a0001 | c0001 | t0002 | g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0008 | a0001 | c0001 | t0002 | g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0009 | a0001 | c0001 | t0002 | g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0010 | a0001 | c0001 | t0002 | g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0011 | a0001 | c0001 | t0002 | g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0012 | a0001 | c0001 | t0002 | g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0013 | a0001 | c0001 | t0002 | g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0014 | a0001 | c0001 | t0002 | g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0015 | a0001 | c0001 | t0002 | g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0016 | a0001 | c0001 | t0002 | g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0017 | a0001 | c0001 | t0002 | g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0018 | a0001 | c0001 | t0002 | g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0019 | a0001 | c0001 | t0002 | g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0020 | a0001 | c0001 | t0002 | g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0021 | a0001 | c0001 | t0002 | g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0002g0022 | a0001 | c0001 | t0002 | g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0003g0082 | a0001 | c0001 | t0003 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0003g0098 | a0001 | c0001 | t0003 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0003g0100 | a0001 | c0001 | t0003 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0003g0102 | a0001 | c0001 | t0003 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0003g0103 | a0001 | c0001 | t0003 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0003g0104 | a0001 | c0001 | t0003 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0003g0105 | a0001 | c0001 | t0003 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0003g0107 | a0001 | c0001 | t0003 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0003g0108 | a0001 | c0001 | t0003 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0003g0110 | a0001 | c0001 | t0003 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0003g0131 | a0001 | c0001 | t0003 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0003g0159 | a0001 | c0001 | t0003 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0003g0169 | a0001 | c0001 | t0003 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0003g0172 | a0001 | c0001 | t0003 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0004g0190 | a0001 | c0001 | t0004 | g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0004g0191 | a0001 | c0001 | t0004 | g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0005g0200 | a0001 | c0001 | t0005 | g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0005g0203 | a0001 | c0001 | t0005 | g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0006g0006 | a0001 | c0001 | t0006 | g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0009g0182 | a0001 | c0001 | t0009 | g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0001t0012g0179 | a0001 | c0001 | t0012 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0003t0001g0005 | a0001 | c0003 | t0001 | g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0003t0001g0219 | a0001 | c0003 | t0001 | g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0003t0001g0220 | a0001 | c0003 | t0001 | g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0003t0001g0221 | a0001 | c0003 | t0001 | g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0004t0001g0081 | a0001 | c0004 | t0001 | g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0004t0001g0092 | a0001 | c0004 | t0001 | g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0004t0001g0093 | a0001 | c0004 | t0001 | g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0004t0001g0111 | a0001 | c0004 | t0001 | g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0005t0001g0153 | a0001 | c0005 | t0001 | g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0005t0001g0156 | a0001 | c0005 | t0001 | g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0005t0001g0157 | a0001 | c0005 | t0001 | g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0005t0001g0158 | a0001 | c0005 | t0001 | g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0006t0001g0231 | a0001 | c0006 | t0001 | g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0006t0001g0232 | a0001 | c0006 | t0001 | g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0006t0001g0233 | a0001 | c0006 | t0001 | g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0006t0010g0234 | a0001 | c0006 | t0010 | g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0007t0001g0215 | a0001 | c0007 | t0001 | g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0007t0001g0216 | a0001 | c0007 | t0001 | g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0007t0001g0217 | a0001 | c0007 | t0001 | g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0012t0001g0147 | a0001 | c0012 | t0001 | g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0013t0001g0193 | a0001 | c0013 | t0001 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0014t0001g0218 | a0001 | c0014 | t0001 | g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0015t0008g0067 | a0001 | c0015 | t0008 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0001c0017t0001g0178 | a0001 | c0017 | t0001 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0002c0002t0001g0051 | a0002 | c0002 | t0001 | g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0002c0002t0001g0066 | a0002 | c0002 | t0001 | g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0002c0002t0001g0072 | a0002 | c0002 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0002c0002t0001g0073 | a0002 | c0002 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0002c0002t0001g0074 | a0002 | c0002 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0002c0002t0001g0076 | a0002 | c0002 | t0001 | g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0002c0002t0001g0091 | a0002 | c0002 | t0001 | g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0002c0002t0007g0037 | a0002 | c0002 | t0007 | g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0003c0009t0001g0175 | a0003 | c0009 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0003c0009t0001g0176 | a0003 | c0009 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0003c0009t0001g0177 | a0003 | c0009 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0004c0008t0001g0039 | a0004 | c0008 | t0001 | g0039 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0004c0008t0001g0094 | a0004 | c0008 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0004c0008t0001g0109 | a0004 | c0008 | t0001 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0005c0010t0001g0063 | a0005 | c0010 | t0001 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0005c0010t0001g0064 | a0005 | c0010 | t0001 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0006c0011t0001g0142 | a0006 | c0011 | t0001 | g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| a0007c0016t0011g0222 | a0007 | c0016 | t0011 | g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | GBR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0012 | EUR | GBR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | CHS | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | CHS | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG00741 | hp1 | a0001 | c0005 | t0001 | g0156 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01071 | hp1 | a0002 | c0002 | t0007 | g0037 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0051 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01358 | hp1 | a0006 | c0011 | t0001 | g0142 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | PEL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01934 | hp2 | a0001 | c0004 | t0001 | g0081 | AMR | PEL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01952 | hp1 | a0001 | c0004 | t0001 | g0093 | AMR | PEL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01952 | hp2 | a0001 | c0012 | t0001 | g0147 | AMR | PEL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01975 | hp2 | a0001 | c0005 | t0001 | g0153 | AMR | PEL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01978 | hp2 | a0001 | c0004 | t0001 | g0092 | AMR | PEL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01981 | hp1 | a0001 | c0005 | t0001 | g0157 | AMR | PEL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0219 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02129 | hp2 | a0001 | c0017 | t0001 | g0178 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02257 | hp2 | a0001 | c0007 | t0001 | g0215 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02258 | hp1 | a0001 | c0006 | t0010 | g0234 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02258 | hp2 | a0004 | c0008 | t0001 | g0109 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02293 | hp1 | a0001 | c0005 | t0001 | g0158 | AMR | PEL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0182 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02572 | hp2 | a0001 | c0006 | t0001 | g0231 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02615 | hp2 | a0005 | c0010 | t0001 | g0063 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02647 | hp1 | a0001 | c0006 | t0001 | g0232 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0073 | SAS | PJL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02717 | hp1 | a0005 | c0010 | t0001 | g0064 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02922 | hp2 | a0001 | c0007 | t0001 | g0217 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02976 | hp2 | a0007 | c0016 | t0011 | g0222 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03130 | hp1 | a0001 | c0006 | t0001 | g0233 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0220 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03195 | hp2 | a0001 | c0007 | t0001 | g0216 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0221 | AFR | MSL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0190 | SAS | STU | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03831 | hp2 | a0004 | c0008 | t0001 | g0094 | SAS | BEB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | STU | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0191 | SAS | STU | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | YRI | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18945 | hp1 | a0003 | c0009 | t0001 | g0177 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18951 | hp1 | a0003 | c0009 | t0001 | g0175 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18999 | hp2 | a0001 | c0001 | t0012 | g0179 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19056 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19081 | hp1 | a0001 | c0013 | t0001 | g0193 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19083 | hp1 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19085 | hp1 | a0003 | c0009 | t0001 | g0176 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0074 | EUR | TSI | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01123 | hp1 | a0001 | c0004 | t0001 | g0111 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02486 | hp2 | a0001 | c0015 | t0008 | g0067 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG06807 | hp1 | a0001 | c0014 | t0001 | g0218 | AFR | USA | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | USA | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | USA | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | USA | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| homoSapiens_chm13v2 | hp1 | a0004 | c0008 | t0001 | g0039 | REF | REF | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0229 | REF | REF | MAP4K5_chr14_50413521_50537569 | MAP4K5 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50434403
|
T | C | 1 | a0005 | 2 | HG02615.hp2 HG02717.hp1 |
missense_variant | MODERATE | c.2155A>G | p.Ile719Val | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/33 | 2386/4270 | 2155/2541 | 719/846 | chr14 | 50434403 | ||
| chr14:50435050
|
G | A | 1 | a0002 | 8 | HG00741.hp2 HG01071.hp1 HG01258.hp1 others(5): Show |
missense_variant | MODERATE | c.1898C>T | p.Thr633Met | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 27/33 | 2129/4270 | 1898/2541 | 633/846 | chr14 | 50435050 | ||
| chr14:50445044
|
T | C | 1 | a0003 | 3 | NA18945.hp1 NA18951.hp1 NA19085.hp1 |
missense_variant | MODERATE | c.1336A>G | p.Ile446Val | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 18/33 | 1567/4270 | 1336/2541 | 446/846 | chr14 | 50445044 | ||
| chr14:50445129
|
A | T | 1 | a0006 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.1251T>A | p.His417Gln | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 18/33 | 1482/4270 | 1251/2541 | 417/846 | chr14 | 50445129 | ||
| chr14:50456531
|
C | T | 1 | a0004 | 3 | HG02258.hp2 HG03831.hp2 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.1000G>A | p.Ala334Thr | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/33 | 1231/4270 | 1000/2541 | 334/846 | chr14 | 50456531 | ||
| chr14:50504845
|
G | A | 1 | a0007 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.121C>T | p.His41Tyr | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/33 | 352/4270 | 121/2541 | 41/846 | chr14 | 50504845 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50429232
|
T | C | 2 | a0001c0003a0001c0006 | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
synonymous_variant | LOW | c.2193A>G | p.Val731Val | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 29/33 | 2424/4270 | 2193/2541 | 731/846 | chr14 | 50429232 | ||
| chr14:50434506
|
T | C | 1 | a0001c0012 | 1 | HG01952.hp2 | synonymous_variant | LOW | c.2052A>G | p.Glu684Glu | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/33 | 2283/4270 | 2052/2541 | 684/846 | chr14 | 50434506 | ||
| chr14:50437528
|
G | A | 1 | a0001c0013 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.1830C>T | p.Phe610Phe | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 26/33 | 2061/4270 | 1830/2541 | 610/846 | chr14 | 50437528 | ||
| chr14:50437534
|
T | C | 3 | a0001c0007a0001c0014a0007c0016 | 5 | HG02257.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.1824A>G | p.Arg608Arg | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 26/33 | 2055/4270 | 1824/2541 | 608/846 | chr14 | 50437534 | ||
| chr14:50440410
|
A | G | 1 | a0001c0004 | 4 | HG01123.hp1 HG01934.hp2 HG01952.hp1 others(1): Show |
synonymous_variant | LOW | c.1596T>C | p.Gly532Gly | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 22/33 | 1827/4270 | 1596/2541 | 532/846 | chr14 | 50440410 | ||
| chr14:50447452
|
T | C | 1 | a0001c0014 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.1104A>G | p.Leu368Leu | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 16/33 | 1335/4270 | 1104/2541 | 368/846 | chr14 | 50447452 | ||
| chr14:50464127
|
T | C | 1 | a0007c0016 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.744A>G | p.Ser248Ser | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/33 | 975/4270 | 744/2541 | 248/846 | chr14 | 50464127 | ||
| chr14:50476165
|
A | G | 1 | a0001c0007 | 3 | HG02257.hp2 HG02922.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.432T>C | p.Ala144Ala | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 8/33 | 663/4270 | 432/2541 | 144/846 | chr14 | 50476165 | ||
| chr14:50486133
|
G | A | 1 | a0001c0005 | 4 | HG00741.hp1 HG01975.hp2 HG01981.hp1 others(1): Show |
synonymous_variant | LOW | c.228C>T | p.Asn76Asn | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 4/33 | 459/4270 | 228/2541 | 76/846 | chr14 | 50486133 | ||
| chr14:50486151
|
T | C | 1 | a0001c0015 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.210A>G | p.Lys70Lys | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 4/33 | 441/4270 | 210/2541 | 70/846 | chr14 | 50486151 | ||
| chr14:50531960
|
G | C | 1 | a0001c0006 | 4 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
synonymous_variant | LOW | c.90C>G | p.Thr30Thr | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/33 | 321/4270 | 90/2541 | 30/846 | chr14 | 50531960 | ||
| chr14:50532013
|
T | G | 2 | a0001c0017a0003c0009 | 4 | HG02129.hp2 NA18945.hp1 NA18951.hp1 others(1): Show |
synonymous_variant | LOW | c.37A>C | p.Arg13Arg | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/33 | 268/4270 | 37/2541 | 13/846 | chr14 | 50532013 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50418817
|
T | C | 1 | a0001c0015t0008 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1202A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 33/33 | 1202 | chr14 | 50418817 | |||||
| chr14:50418882
|
A | T | 1 | a0001c0001t0003 | 14 | HG00408.hp1 HG00423.hp1 NA18939.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1137T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 33/33 | 1137 | chr14 | 50418882 | |||||
| chr14:50419123
|
T | G | 1 | a0001c0001t0009 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*896A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 33/33 | 896 | chr14 | 50419123 | |||||
| chr14:50419169
|
C | A | 1 | a0001c0006t0010 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*850G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 33/33 | 850 | chr14 | 50419169 | |||||
| chr14:50419308
|
T | C | 1 | a0007c0016t0011 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*711A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 33/33 | 711 | chr14 | 50419308 | |||||
| chr14:50419462
|
A | G | 1 | a0001c0001t0005 | 2 | NA18951.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*557T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 33/33 | 557 | chr14 | 50419462 | |||||
| chr14:50419521
|
C | A | 1 | a0007c0016t0011 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*498G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 33/33 | 498 | chr14 | 50419521 | |||||
| chr14:50419560
|
TTC | T | 1 | a0001c0001t0004 | 2 | HG03688.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*457_*458delGA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 33/33 | 457 | chr14 | 50419560 | |||||
| chr14:50532071
|
C | T | 1 | a0002c0002t0007 | 1 | HG01071.hp1 | 5_prime_UTR_variant | MODIFIER | c.-22G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/33 | 22 | chr14 | 50532071 | |||||
| chr14:50532098
|
T | G | 1 | a0001c0001t0012 | 1 | NA18999.hp2 | 5_prime_UTR_variant | MODIFIER | c.-49A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/33 | 49 | chr14 | 50532098 | |||||
| chr14:50532463
|
C | T | 1 | a0001c0001t0002 | 16 | HG00140.hp2 HG00738.hp2 HG01109.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-125G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 1/33 | 414 | chr14 | 50532463 | |||||
| chr14:50532568
|
A | C | 1 | a0001c0001t0006 | 1 | NA19056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-230T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 1/33 | 519 | chr14 | 50532568 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50420234
|
C | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(41): Show | 46 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.2454-128G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50420234 | ||||||
| chr14:50420363
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2454-257C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50420363 | ||||||
| chr14:50420411
|
G | A | 1 | a0007c0016t0011g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2454-305C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50420411 | ||||||
| chr14:50420467
|
C | CA | 25 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(22): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.2454-362dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50420467 | ||||||
| chr14:50420766
|
C | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(42): Show | 47 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.2454-660G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50420766 | ||||||
| chr14:50420898
|
G | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0023others(161): Show | 167 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.2454-792C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50420898 | ||||||
| chr14:50421298
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2454-1192C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50421298 | ||||||
| chr14:50421354
|
G | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(41): Show | 46 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.2454-1248C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50421354 | ||||||
| chr14:50421409
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.2454-1303G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50421409 | ||||||
| chr14:50421669
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 213 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.2453+1452G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50421669 | ||||||
| chr14:50421748
|
C | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 225 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.2453+1373G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50421748 | ||||||
| chr14:50421894
|
CT | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 233 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.2453+1226delA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50421894 | ||||||
| chr14:50422040
|
C | T | 2 | a0001c0006t0001g0231a0001c0006t0010g0234 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2453+1081G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50422040 | ||||||
| chr14:50422098
|
C | T | 1 | a0004c0008t0001g0039 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2453+1023G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50422098 | ||||||
| chr14:50422245
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2453+876A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50422245 | ||||||
| chr14:50422557
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2453+564C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50422557 | ||||||
| chr14:50422648
|
A | G | 2 | a0001c0006t0001g0232a0001c0006t0001g0233 | 2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2453+473T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50422648 | ||||||
| chr14:50422719
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2453+402T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50422719 | ||||||
| chr14:50422734
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2453+387A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50422734 | ||||||
| chr14:50422938
|
CA | C | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2453+182delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 32/32 | chr14 | 50422938 | ||||||
| chr14:50423598
|
T | A | 1 | a0001c0001t0001g0127 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2398-422A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50423598 | ||||||
| chr14:50423607
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 225 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.2398-431C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50423607 | ||||||
| chr14:50423636
|
G | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(41): Show | 46 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.2398-460C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50423636 | ||||||
| chr14:50423663
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2398-487C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50423663 | ||||||
| chr14:50423903
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2398-727C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50423903 | ||||||
| chr14:50424168
|
T | TA | 52 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(49): Show | 54 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.2398-993dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50424168 | ||||||
| chr14:50424168
|
TA | T | 8 | a0001c0001t0001g0129a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG02293.hp2 HG03139.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.2398-993delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50424168 | ||||||
| chr14:50424466
|
T | A | 1 | a0004c0008t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2398-1290A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50424466 | ||||||
| chr14:50424514
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2398-1338T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50424514 | ||||||
| chr14:50424709
|
CA | C | 22 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0180others(19): Show | 23 | HG01256.hp2 HG02055.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.2397+1197delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50424709 | ||||||
| chr14:50424728
|
AG | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(154): Show | 160 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.2397+1178delC | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50424728 | ||||||
| chr14:50424729
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0170 | 2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.2397+1178C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50424729 | ||||||
| chr14:50424771
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0026 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2397+1136T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50424771 | ||||||
| chr14:50424962
|
G | A | 4 | a0001c0004t0001g0081a0001c0004t0001g0092a0001c0004t0001g0093others(1): Show | 4 | HG01123.hp1 HG01934.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.2397+945C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50424962 | ||||||
| chr14:50425073
|
A | G | 2 | a0002c0002t0001g0073a0002c0002t0001g0076 | 2 | HG00741.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.2397+834T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50425073 | ||||||
| chr14:50425096
|
C | T | 43 | a0001c0001t0001g0003a0001c0001t0001g0087a0001c0001t0001g0101others(40): Show | 44 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.2397+811G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50425096 | ||||||
| chr14:50425155
|
GTC | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.2397+750_2397+751d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50425155 | ||||||
| chr14:50425232
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01261.hp2 HG01496.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2397+675C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50425232 | ||||||
| chr14:50425360
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2397+547T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50425360 | ||||||
| chr14:50425539
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2397+368T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50425539 | ||||||
| chr14:50425780
|
T | C | 6 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2397+127A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50425780 | ||||||
| chr14:50425887
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2397+20C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50425887 | ||||||
| chr14:50425893
|
C | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0187others(2): Show | 5 | HG00733.hp2 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2397+14G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 31/32 | chr14 | 50425893 | ||||||
| chr14:50426008
|
T | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(22): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.2327-31A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50426008 | ||||||
| chr14:50426508
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2327-531A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50426508 | ||||||
| chr14:50426596
|
T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 230 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2327-619A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50426596 | ||||||
| chr14:50426598
|
C | T | 4 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0199others(1): Show | 4 | NA18940.hp2 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.2327-621G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50426598 | ||||||
| chr14:50426630
|
G | C | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2327-653C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50426630 | ||||||
| chr14:50426651
|
C | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 233 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.2327-674G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50426651 | ||||||
| chr14:50426654
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2327-677C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50426654 | ||||||
| chr14:50426840
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0026 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2327-863A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50426840 | ||||||
| chr14:50427091
|
AT | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0050a0001c0001t0001g0062others(1): Show | 4 | HG01069.hp2 HG01346.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2327-1115delA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50427091 | ||||||
| chr14:50427126
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2327-1149G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50427126 | ||||||
| chr14:50427140
|
C | T | 4 | a0001c0006t0001g0231a0001c0006t0001g0232a0001c0006t0001g0233others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2327-1163G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50427140 | ||||||
| chr14:50427547
|
T | A | 1 | a0001c0001t0001g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2326+1115A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50427547 | ||||||
| chr14:50427710
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(42): Show | 47 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.2326+952A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50427710 | ||||||
| chr14:50427733
|
T | A | 3 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG01358.hp2 HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2326+929A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50427733 | ||||||
| chr14:50427738
|
A | G | 44 | a0001c0001t0001g0003a0001c0001t0001g0087a0001c0001t0001g0101others(41): Show | 45 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.2326+924T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50427738 | ||||||
| chr14:50427874
|
T | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.2326+788A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50427874 | ||||||
| chr14:50428220
|
T | C | 8 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(5): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2326+442A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50428220 | ||||||
| chr14:50428270
|
CT | C | 6 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2326+391delA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50428270 | ||||||
| chr14:50428397
|
A | C | 1 | a0001c0001t0001g0154 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2326+265T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50428397 | ||||||
| chr14:50428450
|
TTC | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 225 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.2326+210_2326+211d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50428450 | ||||||
| chr14:50428508
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2326+154C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50428508 | ||||||
| chr14:50428556
|
C | T | 1 | a0005c0010t0001g0064 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2326+106G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50428556 | ||||||
| chr14:50428624
|
A | G | 3 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217 | 3 | HG02257.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2326+38T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50428624 | ||||||
| chr14:50428630
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0002g0015 | 2 | HG01361.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.2326+32C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 30/32 | chr14 | 50428630 | ||||||
| chr14:50428769
|
ACAAGT | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG00733.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2234-20_2234-16del others(5): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 29/32 | chr14 | 50428769 | ||||||
| chr14:50428976
|
T | C | 7 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0183others(4): Show | 7 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2233+216A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 29/32 | chr14 | 50428976 | ||||||
| chr14:50429090
|
T | C | 1 | a0003c0009t0001g0177 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2233+102A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 29/32 | chr14 | 50429090 | ||||||
| chr14:50429716
|
T | C | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG00733.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2165-456A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50429716 | ||||||
| chr14:50429792
|
G | A | 5 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(2): Show | 5 | HG02976.hp2 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2165-532C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50429792 | ||||||
| chr14:50429878
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0026 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2165-618T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50429878 | ||||||
| chr14:50429944
|
T | C | 1 | a0002c0002t0001g0076 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2165-684A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50429944 | ||||||
| chr14:50430080
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2165-820A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50430080 | ||||||
| chr14:50430201
|
T | A | 1 | a0001c0001t0001g0133 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2165-941A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50430201 | ||||||
| chr14:50430458
|
G | A | 1 | a0001c0001t0003g0159 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2165-1198C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50430458 | ||||||
| chr14:50430497
|
G | A | 1 | a0006c0011t0001g0142 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2165-1237C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50430497 | ||||||
| chr14:50430570
|
C | G | 1 | a0004c0008t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2165-1310G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50430570 | ||||||
| chr14:50430599
|
C | A | 1 | a0001c0001t0004g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2165-1339G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50430599 | ||||||
| chr14:50430911
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2165-1651C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50430911 | ||||||
| chr14:50430925
|
T | C | 115 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0041others(112): Show | 115 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.2165-1665A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50430925 | ||||||
| chr14:50431060
|
C | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.2165-1800G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50431060 | ||||||
| chr14:50431124
|
A | G | 1 | a0001c0001t0003g0103 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2165-1864T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50431124 | ||||||
| chr14:50431141
|
T | C | 4 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(1): Show | 5 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2165-1881A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50431141 | ||||||
| chr14:50431348
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2165-2088G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50431348 | ||||||
| chr14:50431359
|
G | A | 11 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(8): Show | 12 | HG02055.hp2 HG02257.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.2165-2099C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50431359 | ||||||
| chr14:50431468
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2165-2208C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50431468 | ||||||
| chr14:50431561
|
G | A | 4 | a0001c0006t0001g0231a0001c0006t0001g0232a0001c0006t0001g0233others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2165-2301C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50431561 | ||||||
| chr14:50431582
|
T | C | 1 | a0001c0001t0002g0018 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2165-2322A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50431582 | ||||||
| chr14:50431603
|
C | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(4): Show | 7 | HG00733.hp1 HG00735.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2165-2343G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50431603 | ||||||
| chr14:50431651
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2165-2391C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50431651 | ||||||
| chr14:50431656
|
T | G | 1 | a0002c0002t0001g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2165-2396A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50431656 | ||||||
| chr14:50431697
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.2165-2437T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50431697 | ||||||
| chr14:50431701
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.2165-2441A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50431701 | ||||||
| chr14:50431742
|
A | G | 44 | a0001c0001t0001g0003a0001c0001t0001g0087a0001c0001t0001g0101others(41): Show | 45 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.2165-2482T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50431742 | ||||||
| chr14:50431822
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0026 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2165-2562G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50431822 | ||||||
| chr14:50432030
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2164+2364G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50432030 | ||||||
| chr14:50432085
|
G | T | 1 | a0001c0001t0001g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2164+2309C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50432085 | ||||||
| chr14:50432424
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0026 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2164+1970C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50432424 | ||||||
| chr14:50432457
|
G | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(7): Show | 11 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.2164+1937C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50432457 | ||||||
| chr14:50432556
|
C | CA | 5 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0034others(2): Show | 6 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2164+1837dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50432556 | ||||||
| chr14:50432556
|
CA | C | 12 | a0001c0001t0001g0161a0001c0001t0001g0183a0001c0001t0001g0225others(9): Show | 13 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2164+1837delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50432556 | ||||||
| chr14:50432556
|
CAA | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(163): Show | 169 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.2164+1836_2164+183 others(6): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50432556 | ||||||
| chr14:50432556
|
CAAA | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(23): Show | 27 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.2164+1835_2164+183 others(7): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50432556 | ||||||
| chr14:50432568
|
A | C | 2 | a0001c0006t0001g0231a0001c0006t0010g0234 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2164+1826T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50432568 | ||||||
| chr14:50432569
|
A | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(154): Show | 160 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.2164+1825T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50432569 | ||||||
| chr14:50432576
|
AC | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0006t0001g0232 | 3 | HG01261.hp2 HG01496.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2164+1817delG | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50432576 | ||||||
| chr14:50432577
|
C | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(8): Show | 12 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2164+1817G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50432577 | ||||||
| chr14:50432682
|
G | C | 1 | a0001c0001t0001g0208 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2164+1712C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50432682 | ||||||
| chr14:50432940
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2164+1454G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50432940 | ||||||
| chr14:50432984
|
T | C | 32 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(29): Show | 33 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.2164+1410A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50432984 | ||||||
| chr14:50433174
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2164+1220C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50433174 | ||||||
| chr14:50433292
|
G | A | 4 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217others(1): Show | 4 | HG02257.hp2 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164+1102C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50433292 | ||||||
| chr14:50433491
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2164+903A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50433491 | ||||||
| chr14:50433555
|
T | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(1): Show | 4 | HG02523.hp2 NA18944.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.2164+839A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50433555 | ||||||
| chr14:50433796
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2164+598G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50433796 | ||||||
| chr14:50433813
|
G | C | 1 | a0001c0001t0001g0181 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2164+581C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50433813 | ||||||
| chr14:50434028
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(28): Show | 32 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.2164+366C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50434028 | ||||||
| chr14:50434160
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2164+234A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50434160 | ||||||
| chr14:50434283
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2164+111A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50434283 | ||||||
| chr14:50434294
|
A | G | 14 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(11): Show | 15 | HG02055.hp2 HG02257.hp2 HG02896.hp2 others(12): Show |
intron_variant | MODIFIER | c.2164+100T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 28/32 | chr14 | 50434294 | ||||||
| chr14:50434814
|
A | T | 4 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217others(1): Show | 4 | HG02257.hp2 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1986+148T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 27/32 | chr14 | 50434814 | ||||||
| chr14:50434941
|
T | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228 | 3 | HG03139.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1986+21A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 27/32 | chr14 | 50434941 | ||||||
| chr14:50435085
|
CA | C | 4 | a0001c0006t0001g0231a0001c0006t0001g0232a0001c0006t0001g0233others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1883-21delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 26/32 | chr14 | 50435085 | ||||||
| chr14:50435257
|
A | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0056a0001c0001t0001g0077 | 5 | HG01884.hp2 HG02559.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883-192T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 26/32 | chr14 | 50435257 | ||||||
| chr14:50435361
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0026 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1883-296C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 26/32 | chr14 | 50435361 | ||||||
| chr14:50435539
|
A | AT | 6 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1883-475dupA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 26/32 | chr14 | 50435539 | ||||||
| chr14:50435726
|
A | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(22): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.1883-661T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 26/32 | chr14 | 50435726 | ||||||
| chr14:50436074
|
T | C | 2 | a0002c0002t0001g0051a0002c0002t0001g0066 | 2 | HG01258.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1883-1009A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 26/32 | chr14 | 50436074 | ||||||
| chr14:50436101
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 197 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1883-1036A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 26/32 | chr14 | 50436101 | ||||||
| chr14:50436129
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1883-1064A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 26/32 | chr14 | 50436129 | ||||||
| chr14:50436153
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(158): Show | 164 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1883-1088A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 26/32 | chr14 | 50436153 | ||||||
| chr14:50436324
|
T | G | 1 | a0001c0001t0001g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1882+1152A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 26/32 | chr14 | 50436324 | ||||||
| chr14:50436697
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(218): Show | 227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.1882+779G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 26/32 | chr14 | 50436697 | ||||||
| chr14:50436705
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1882+771C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 26/32 | chr14 | 50436705 | ||||||
| chr14:50437406
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1882+70G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 26/32 | chr14 | 50437406 | ||||||
| chr14:50437586
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1824-52T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 25/32 | chr14 | 50437586 | ||||||
| chr14:50437849
|
A | G | 3 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217 | 3 | HG02257.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1823+45T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 25/32 | chr14 | 50437849 | ||||||
| chr14:50438136
|
T | G | 1 | a0001c0001t0001g0036 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1706-42A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 23/32 | chr14 | 50438136 | ||||||
| chr14:50438386
|
T | A | 1 | a0001c0001t0001g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1706-292A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 23/32 | chr14 | 50438386 | ||||||
| chr14:50438403
|
G | T | 1 | a0001c0001t0005g0200 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1706-309C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 23/32 | chr14 | 50438403 | ||||||
| chr14:50438567
|
A | C | 21 | a0001c0001t0001g0140a0001c0001t0001g0192a0001c0001t0001g0194others(18): Show | 21 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(18): Show |
intron_variant | MODIFIER | c.1706-473T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 23/32 | chr14 | 50438567 | ||||||
| chr14:50438575
|
G | A | 1 | a0001c0001t0003g0108 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1706-481C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 23/32 | chr14 | 50438575 | ||||||
| chr14:50438967
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(158): Show | 164 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1706-873A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 23/32 | chr14 | 50438967 | ||||||
| chr14:50438999
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1706-905C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 23/32 | chr14 | 50438999 | ||||||
| chr14:50439021
|
T | TA | 4 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(1): Show | 5 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1706-928dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 23/32 | chr14 | 50439021 | ||||||
| chr14:50439073
|
G | T | 16 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0002g0007others(13): Show | 16 | HG00140.hp2 HG00738.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1705+940C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 23/32 | chr14 | 50439073 | ||||||
| chr14:50439333
|
TA | T | 5 | a0001c0001t0004g0190a0001c0001t0004g0191a0001c0001t0005g0200others(2): Show | 5 | HG01975.hp2 HG03688.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1705+679delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 23/32 | chr14 | 50439333 | ||||||
| chr14:50439372
|
C | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(158): Show | 164 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1705+641G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 23/32 | chr14 | 50439372 | ||||||
| chr14:50439398
|
A | G | 4 | a0001c0006t0001g0231a0001c0006t0001g0232a0001c0006t0001g0233others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1705+615T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 23/32 | chr14 | 50439398 | ||||||
| chr14:50439624
|
TGA | T | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228 | 3 | HG03139.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1705+387_1705+388d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 23/32 | chr14 | 50439624 | ||||||
| chr14:50439736
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1705+277C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 23/32 | chr14 | 50439736 | ||||||
| chr14:50439753
|
C | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(158): Show | 164 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1705+260G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 23/32 | chr14 | 50439753 | ||||||
| chr14:50440622
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1565-181T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50440622 | ||||||
| chr14:50440704
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0002g0015 | 2 | HG01361.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1565-263T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50440704 | ||||||
| chr14:50440775
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.1565-334C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50440775 | ||||||
| chr14:50441067
|
C | G | 7 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(4): Show | 8 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1565-626G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441067 | ||||||
| chr14:50441120
|
C | T | 4 | a0001c0006t0001g0231a0001c0006t0001g0232a0001c0006t0001g0233others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1565-679G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441120 | ||||||
| chr14:50441359
|
C | T | 1 | a0001c0005t0001g0153 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1565-918G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441359 | ||||||
| chr14:50441474
|
A | C | 3 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217 | 3 | HG02257.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1565-1033T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441474 | ||||||
| chr14:50441555
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1565-1114T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441555 | ||||||
| chr14:50441668
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1564+1064A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441668 | ||||||
| chr14:50441733
|
A | T | 1 | a0001c0001t0001g0040 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1564+999T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441733 | ||||||
| chr14:50441743
|
TAC | T | 10 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0028others(7): Show | 10 | HG01496.hp2 HG01978.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.1564+987_1564+988d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441743 | ||||||
| chr14:50441743
|
TACAC | T | 14 | a0001c0001t0001g0035a0001c0001t0001g0084a0001c0001t0001g0106others(11): Show | 14 | HG00423.hp1 HG00733.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1564+985_1564+988d others(6): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441743 | ||||||
| chr14:50441743
|
TACACAC | T | 10 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0095others(7): Show | 11 | HG01952.hp1 HG02055.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1564+983_1564+988d others(8): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441743 | ||||||
| chr14:50441743
|
TACACACA others(1): Show |
T | 11 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0060others(8): Show | 11 | HG01074.hp2 HG01243.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.1564+981_1564+988d others(10): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441743 | ||||||
| chr14:50441743
|
TACACACA others(3): Show |
T | 20 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0083others(17): Show | 20 | HG00140.hp2 HG01071.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.1564+979_1564+988d others(12): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441743 | ||||||
| chr14:50441743
|
TACACACA others(5): Show |
T | 41 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0057others(38): Show | 42 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.1564+977_1564+988d others(14): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441743 | ||||||
| chr14:50441743
|
TACACACA others(7): Show |
T | 24 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0038others(21): Show | 24 | HG00733.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1564+975_1564+988d others(16): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441743 | ||||||
| chr14:50441743
|
TACACACA others(9): Show |
T | 40 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0042others(37): Show | 42 | HG00735.hp1 HG01109.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1564+973_1564+988d others(18): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441743 | ||||||
| chr14:50441743
|
TACACACA others(11): Show |
T | 5 | a0001c0001t0001g0046a0001c0001t0001g0065a0001c0001t0002g0010others(2): Show | 5 | HG01261.hp1 HG01884.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1564+971_1564+988d others(20): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441743 | ||||||
| chr14:50441743
|
TACACACA others(13): Show |
T | 8 | a0001c0001t0001g0004a0001c0001t0001g0056a0001c0001t0001g0077others(5): Show | 9 | HG00140.hp1 HG00423.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1564+969_1564+988d others(22): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441743 | ||||||
| chr14:50441743
|
TACACACA others(15): Show |
T | 22 | a0001c0001t0001g0053a0001c0001t0001g0192a0001c0001t0001g0194others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1564+967_1564+988d others(24): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441743 | ||||||
| chr14:50441743
|
TACACACA others(19): Show |
T | 1 | a0001c0001t0001g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1564+963_1564+988d others(28): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441743 | ||||||
| chr14:50441771
|
CACACACA others(21): Show |
C | 3 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217 | 3 | HG02257.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1564+933_1564+960d others(30): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441771 | ||||||
| chr14:50441773
|
CACACACA others(19): Show |
C | 4 | a0001c0006t0001g0231a0001c0006t0001g0232a0001c0006t0001g0233others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1564+933_1564+958d others(28): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441773 | ||||||
| chr14:50441779
|
CACACACA others(13): Show |
C | 2 | a0001c0001t0001g0180a0001c0001t0009g0182 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1564+933_1564+952d others(22): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441779 | ||||||
| chr14:50441783
|
CACACACA others(9): Show |
C | 2 | a0001c0001t0001g0183a0001c0001t0001g0186 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1564+933_1564+948d others(18): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441783 | ||||||
| chr14:50441785
|
CACACACA others(7): Show |
C | 1 | a0001c0001t0001g0184 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1564+933_1564+946d others(16): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441785 | ||||||
| chr14:50441787
|
CACACACA others(5): Show |
C | 2 | a0001c0001t0001g0163a0001c0001t0001g0185 | 2 | HG01361.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1564+933_1564+944d others(14): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441787 | ||||||
| chr14:50441789
|
CACACACA others(3): Show |
C | 1 | a0001c0001t0004g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1564+933_1564+942d others(12): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441789 | ||||||
| chr14:50441979
|
C | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(28): Show | 32 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.1564+753G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50441979 | ||||||
| chr14:50442145
|
TAA | T | 3 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220 | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1564+585_1564+586d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50442145 | ||||||
| chr14:50442450
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1564+282G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50442450 | ||||||
| chr14:50442692
|
AT | A | 4 | a0001c0006t0001g0231a0001c0006t0001g0232a0001c0006t0001g0233others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1564+39delA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | 50442692 | ||||||
| chr14:50442847
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0026 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1480-31A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 20/32 | chr14 | 50442847 | ||||||
| chr14:50442937
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1480-121A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 20/32 | chr14 | 50442937 | ||||||
| chr14:50443350
|
G | GA | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(218): Show | 226 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1479+378dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 20/32 | chr14 | 50443350 | ||||||
| chr14:50443522
|
C | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.1479+207G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 20/32 | chr14 | 50443522 | ||||||
| chr14:50443584
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1479+145G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 20/32 | chr14 | 50443584 | ||||||
| chr14:50444083
|
T | C | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1340-47A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 18/32 | chr14 | 50444083 | ||||||
| chr14:50444283
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1340-247G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 18/32 | chr14 | 50444283 | ||||||
| chr14:50444462
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.1340-426T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 18/32 | chr14 | 50444462 | ||||||
| chr14:50444465
|
A | G | 4 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(1): Show | 5 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1340-429T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 18/32 | chr14 | 50444465 | ||||||
| chr14:50444477
|
G | A | 7 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(4): Show | 8 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1340-441C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 18/32 | chr14 | 50444477 | ||||||
| chr14:50444972
|
T | A | 1 | a0001c0001t0001g0168 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1339+69A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 18/32 | chr14 | 50444972 | ||||||
| chr14:50445288
|
T | C | 4 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(1): Show | 5 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1186-94A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 17/32 | chr14 | 50445288 | ||||||
| chr14:50445404
|
C | T | 6 | a0001c0001t0001g0180a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1186-210G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 17/32 | chr14 | 50445404 | ||||||
| chr14:50445485
|
A | C | 1 | a0001c0001t0002g0007 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1186-291T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 17/32 | chr14 | 50445485 | ||||||
| chr14:50445493
|
G | A | 1 | a0001c0014t0001g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1186-299C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 17/32 | chr14 | 50445493 | ||||||
| chr14:50445572
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1186-378A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 17/32 | chr14 | 50445572 | ||||||
| chr14:50445718
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1185+361G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 17/32 | chr14 | 50445718 | ||||||
| chr14:50445839
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 9 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1185+240A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 17/32 | chr14 | 50445839 | ||||||
| chr14:50445870
|
C | T | 1 | a0001c0006t0001g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1185+209G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 17/32 | chr14 | 50445870 | ||||||
| chr14:50445899
|
T | C | 1 | a0007c0016t0011g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1185+180A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 17/32 | chr14 | 50445899 | ||||||
| chr14:50446182
|
T | C | 3 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217 | 3 | HG02257.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1143-61A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 16/32 | chr14 | 50446182 | ||||||
| chr14:50446236
|
T | C | 3 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | NA18940.hp2 NA18960.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1143-115A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 16/32 | chr14 | 50446236 | ||||||
| chr14:50446239
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1143-118G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 16/32 | chr14 | 50446239 | ||||||
| chr14:50446566
|
G | C | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228 | 3 | HG03139.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1143-445C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 16/32 | chr14 | 50446566 | ||||||
| chr14:50446806
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1142+608G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 16/32 | chr14 | 50446806 | ||||||
| chr14:50446950
|
T | C | 1 | a0001c0001t0002g0007 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1142+464A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 16/32 | chr14 | 50446950 | ||||||
| chr14:50446989
|
A | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(10): Show | 14 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1142+425T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 16/32 | chr14 | 50446989 | ||||||
| chr14:50447228
|
A | G | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG00733.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1142+186T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 16/32 | chr14 | 50447228 | ||||||
| chr14:50447310
|
T | C | 23 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(20): Show | 24 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.1142+104A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 16/32 | chr14 | 50447310 | ||||||
| chr14:50447881
|
T | G | 1 | a0001c0015t0008g0067 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1075-400A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 15/32 | chr14 | 50447881 | ||||||
| chr14:50447902
|
CAT | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 213 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1075-423_1075-422d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 15/32 | chr14 | 50447902 | ||||||
| chr14:50448030
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.1075-549A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 15/32 | chr14 | 50448030 | ||||||
| chr14:50448037
|
TCA | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.1075-558_1075-557d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 15/32 | chr14 | 50448037 | ||||||
| chr14:50448203
|
C | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 16 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1074+571G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 15/32 | chr14 | 50448203 | ||||||
| chr14:50448296
|
T | C | 3 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217 | 3 | HG02257.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1074+478A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 15/32 | chr14 | 50448296 | ||||||
| chr14:50448519
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1074+255G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 15/32 | chr14 | 50448519 | ||||||
| chr14:50448576
|
T | C | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1074+198A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 15/32 | chr14 | 50448576 | ||||||
| chr14:50448596
|
G | A | 15 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 16 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1074+178C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 15/32 | chr14 | 50448596 | ||||||
| chr14:50448714
|
CA | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 9 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1074+59delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 15/32 | chr14 | 50448714 | ||||||
| chr14:50449052
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0056 | 4 | HG01884.hp2 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016-220A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50449052 | ||||||
| chr14:50449207
|
T | A | 1 | a0001c0001t0001g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1016-375A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50449207 | ||||||
| chr14:50449338
|
A | C | 1 | a0001c0001t0002g0022 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1016-506T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50449338 | ||||||
| chr14:50449376
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 9 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1016-544T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50449376 | ||||||
| chr14:50449420
|
C | T | 2 | a0001c0006t0001g0232a0001c0006t0001g0233 | 2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1016-588G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50449420 | ||||||
| chr14:50449491
|
T | C | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1016-659A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50449491 | ||||||
| chr14:50449638
|
C | T | 1 | a0001c0003t0001g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1016-806G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50449638 | ||||||
| chr14:50449725
|
AT | A | 19 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(16): Show | 19 | HG00733.hp1 HG01069.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1016-894delA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50449725 | ||||||
| chr14:50449759
|
A | G | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1016-927T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50449759 | ||||||
| chr14:50449937
|
TTTGTTG | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG00733.hp1 HG01109.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016-1111_1016-110 others(10): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50449937 | ||||||
| chr14:50449939
|
TG | T | 30 | a0001c0001t0001g0060a0001c0001t0001g0083a0001c0001t0001g0084others(27): Show | 30 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.1016-1108delC | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50449939 | ||||||
| chr14:50449940
|
G | T | 9 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(6): Show | 9 | HG01358.hp2 HG01433.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1016-1108C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50449940 | ||||||
| chr14:50450037
|
G | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(2): Show | 5 | HG00140.hp2 HG00738.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1016-1205C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50450037 | ||||||
| chr14:50450224
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(28): Show | 32 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.1016-1392C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50450224 | ||||||
| chr14:50450385
|
T | G | 15 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 16 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1016-1553A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50450385 | ||||||
| chr14:50450420
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01261.hp2 HG01496.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1016-1588T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50450420 | ||||||
| chr14:50450542
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1016-1710C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50450542 | ||||||
| chr14:50450617
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1016-1785A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50450617 | ||||||
| chr14:50450672
|
G | C | 1 | a0002c0002t0001g0074 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1016-1840C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50450672 | ||||||
| chr14:50450732
|
G | A | 1 | a0001c0003t0001g0005 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1016-1900C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50450732 | ||||||
| chr14:50450787
|
C | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(20): Show | 24 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.1016-1955G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50450787 | ||||||
| chr14:50451147
|
C | A | 1 | a0001c0001t0003g0104 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1016-2315G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50451147 | ||||||
| chr14:50451211
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01069.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1016-2379T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50451211 | ||||||
| chr14:50451227
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1016-2395C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50451227 | ||||||
| chr14:50451229
|
C | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(158): Show | 164 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1016-2397G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50451229 | ||||||
| chr14:50451258
|
G | GA | 25 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(22): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.1016-2427dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50451258 | ||||||
| chr14:50451320
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(22): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.1016-2488G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50451320 | ||||||
| chr14:50451349
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1016-2517G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50451349 | ||||||
| chr14:50451589
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1016-2757A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50451589 | ||||||
| chr14:50451737
|
A | C | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1016-2905T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50451737 | ||||||
| chr14:50451774
|
T | C | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1016-2942A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50451774 | ||||||
| chr14:50451784
|
A | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 180 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.1016-2952T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50451784 | ||||||
| chr14:50451834
|
T | A | 1 | a0001c0001t0001g0095 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1016-3002A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50451834 | ||||||
| chr14:50451871
|
T | C | 1 | a0001c0001t0002g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1016-3039A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50451871 | ||||||
| chr14:50451940
|
G | C | 1 | a0001c0001t0001g0099 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1016-3108C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50451940 | ||||||
| chr14:50452078
|
A | G | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1016-3246T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50452078 | ||||||
| chr14:50452108
|
G | T | 1 | a0001c0001t0001g0096 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1016-3276C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50452108 | ||||||
| chr14:50452175
|
T | C | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1016-3343A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50452175 | ||||||
| chr14:50452412
|
G | A | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1016-3580C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50452412 | ||||||
| chr14:50452437
|
T | C | 2 | a0001c0006t0001g0232a0001c0006t0001g0233 | 2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1016-3605A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50452437 | ||||||
| chr14:50452567
|
A | G | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1016-3735T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50452567 | ||||||
| chr14:50452590
|
C | G | 1 | a0001c0001t0001g0138 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1016-3758G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50452590 | ||||||
| chr14:50452653
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1016-3821A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50452653 | ||||||
| chr14:50452738
|
C | A | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0078others(2): Show | 5 | HG01433.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1015+3778G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50452738 | ||||||
| chr14:50452896
|
T | C | 1 | a0002c0002t0001g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1015+3620A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50452896 | ||||||
| chr14:50453016
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1015+3500A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50453016 | ||||||
| chr14:50453079
|
A | T | 4 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217others(1): Show | 4 | HG02257.hp2 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015+3437T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50453079 | ||||||
| chr14:50453093
|
A | ATG | 25 | a0001c0001t0001g0095a0001c0001t0001g0117a0001c0001t0001g0118others(22): Show | 25 | HG01123.hp1 HG01123.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1015+3421_1015+342 others(6): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50453093 | ||||||
| chr14:50453155
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1015+3361G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50453155 | ||||||
| chr14:50453377
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1015+3139C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50453377 | ||||||
| chr14:50453678
|
A | T | 1 | a0001c0001t0001g0088 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1015+2838T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50453678 | ||||||
| chr14:50453711
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 225 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.1015+2805C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50453711 | ||||||
| chr14:50453875
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 222 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.1015+2641C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50453875 | ||||||
| chr14:50453978
|
A | C | 1 | a0001c0001t0001g0162 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1015+2538T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50453978 | ||||||
| chr14:50454153
|
C | A | 3 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217 | 3 | HG02257.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1015+2363G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50454153 | ||||||
| chr14:50454160
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1015+2356G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50454160 | ||||||
| chr14:50454491
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1015+2025A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50454491 | ||||||
| chr14:50454608
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1015+1908G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50454608 | ||||||
| chr14:50454635
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1015+1881C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50454635 | ||||||
| chr14:50454827
|
CTTAAGTT others(10): Show |
C | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG00733.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1015+1672_1015+168 others(21): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50454827 | ||||||
| chr14:50454846
|
G | T | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG00733.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1015+1670C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50454846 | ||||||
| chr14:50455224
|
T | C | 1 | a0001c0015t0008g0067 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1015+1292A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50455224 | ||||||
| chr14:50455500
|
C | T | 1 | a0002c0002t0001g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1015+1016G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50455500 | ||||||
| chr14:50455851
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1015+665C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50455851 | ||||||
| chr14:50455890
|
G | A | 4 | a0001c0006t0001g0231a0001c0006t0001g0232a0001c0006t0001g0233others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1015+626C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50455890 | ||||||
| chr14:50456057
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1015+459T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50456057 | ||||||
| chr14:50456269
|
C | A | 1 | a0006c0011t0001g0142 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1015+247G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 14/32 | chr14 | 50456269 | ||||||
| chr14:50456619
|
T | C | 1 | a0001c0005t0001g0158 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.937-25A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50456619 | ||||||
| chr14:50456706
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.937-112C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50456706 | ||||||
| chr14:50456746
|
C | T | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG00733.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.937-152G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50456746 | ||||||
| chr14:50456747
|
G | A | 3 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080 | 3 | HG01433.hp2 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.937-153C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50456747 | ||||||
| chr14:50456953
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.937-359C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50456953 | ||||||
| chr14:50457346
|
G | T | 4 | a0001c0006t0001g0231a0001c0006t0001g0232a0001c0006t0001g0233others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.937-752C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50457346 | ||||||
| chr14:50457625
|
ACT | A | 7 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | HG02976.hp2 HG03139.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.937-1033_937-1032d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50457625 | ||||||
| chr14:50457722
|
C | T | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG00733.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.937-1128G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50457722 | ||||||
| chr14:50457732
|
G | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(10): Show | 14 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.937-1138C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50457732 | ||||||
| chr14:50457857
|
T | C | 12 | a0001c0001t0001g0057a0001c0003t0001g0005a0001c0003t0001g0219others(9): Show | 13 | HG02055.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.937-1263A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50457857 | ||||||
| chr14:50457999
|
G | A | 4 | a0001c0001t0001g0057a0001c0007t0001g0215a0001c0007t0001g0216others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-1405C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50457999 | ||||||
| chr14:50458033
|
C | T | 1 | a0001c0001t0003g0098 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.937-1439G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50458033 | ||||||
| chr14:50458093
|
C | T | 21 | a0001c0001t0001g0140a0001c0001t0001g0192a0001c0001t0001g0194others(18): Show | 21 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(18): Show |
intron_variant | MODIFIER | c.937-1499G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50458093 | ||||||
| chr14:50458109
|
C | T | 1 | a0001c0014t0001g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.937-1515G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50458109 | ||||||
| chr14:50458191
|
T | C | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228 | 3 | HG03139.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.937-1597A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50458191 | ||||||
| chr14:50458208
|
A | G | 8 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(5): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.937-1614T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50458208 | ||||||
| chr14:50458548
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.937-1954G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50458548 | ||||||
| chr14:50458679
|
G | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 229 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.937-2085C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50458679 | ||||||
| chr14:50458835
|
G | A | 1 | a0004c0008t0001g0039 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.937-2241C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50458835 | ||||||
| chr14:50458837
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.937-2243G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50458837 | ||||||
| chr14:50459161
|
A | C | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.937-2567T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50459161 | ||||||
| chr14:50459213
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.937-2619G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50459213 | ||||||
| chr14:50459566
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.937-2972G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50459566 | ||||||
| chr14:50459699
|
C | CTT | 46 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0042others(43): Show | 47 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.936+2964_936+2965d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50459699 | ||||||
| chr14:50459701
|
T | C | 1 | a0007c0016t0011g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.936+2964A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50459701 | ||||||
| chr14:50459843
|
G | A | 2 | a0001c0014t0001g0218a0007c0016t0011g0222 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.936+2822C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50459843 | ||||||
| chr14:50459919
|
T | C | 8 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(5): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.936+2746A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50459919 | ||||||
| chr14:50460030
|
C | T | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228 | 3 | HG03139.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.936+2635G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50460030 | ||||||
| chr14:50460277
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.936+2388G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50460277 | ||||||
| chr14:50460278
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.936+2387C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50460278 | ||||||
| chr14:50460319
|
GC | G | 11 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0003t0001g0005others(8): Show | 12 | HG02055.hp2 HG02257.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.936+2345delG | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50460319 | ||||||
| chr14:50460474
|
C | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(29): Show | 33 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.936+2191G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50460474 | ||||||
| chr14:50460603
|
G | A | 2 | a0001c0014t0001g0218a0007c0016t0011g0222 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.936+2062C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50460603 | ||||||
| chr14:50460874
|
T | TG | 43 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(40): Show | 45 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.936+1790dupC | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50460874 | ||||||
| chr14:50460992
|
T | C | 4 | a0001c0001t0002g0020a0001c0007t0001g0215a0001c0007t0001g0216others(1): Show | 4 | HG02074.hp1 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+1673A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50460992 | ||||||
| chr14:50461023
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.936+1642A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50461023 | ||||||
| chr14:50461171
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0097 | 2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.936+1494C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50461171 | ||||||
| chr14:50461447
|
T | C | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.936+1218A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50461447 | ||||||
| chr14:50461501
|
G | A | 1 | a0001c0015t0008g0067 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.936+1164C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50461501 | ||||||
| chr14:50461538
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.936+1127A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50461538 | ||||||
| chr14:50461699
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0040others(114): Show | 119 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.936+966A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50461699 | ||||||
| chr14:50461779
|
C | T | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.936+886G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50461779 | ||||||
| chr14:50461827
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.936+838C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50461827 | ||||||
| chr14:50461896
|
C | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0115a0001c0001t0001g0135others(41): Show | 45 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.936+769G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50461896 | ||||||
| chr14:50462011
|
A | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.936+654T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50462011 | ||||||
| chr14:50462135
|
C | T | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.936+530G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50462135 | ||||||
| chr14:50462136
|
G | A | 1 | a0001c0006t0010g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.936+529C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50462136 | ||||||
| chr14:50462139
|
G | A | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG00733.hp2 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.936+526C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50462139 | ||||||
| chr14:50462164
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.936+501A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50462164 | ||||||
| chr14:50462526
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.936+139C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50462526 | ||||||
| chr14:50462555
|
C | T | 1 | a0002c0002t0001g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.936+110G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 13/32 | chr14 | 50462555 | ||||||
| chr14:50462790
|
C | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.820-9G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50462790 | ||||||
| chr14:50462912
|
T | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(10): Show | 14 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.820-131A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50462912 | ||||||
| chr14:50463135
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01261.hp2 HG01496.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.820-354T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463135 | ||||||
| chr14:50463258
|
CACTG | C | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG00733.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.820-481_820-478del others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463258 | ||||||
| chr14:50463301
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.820-520A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463301 | ||||||
| chr14:50463492
|
T | A | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.819+560A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463492 | ||||||
| chr14:50463494
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.819+558T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463494 | ||||||
| chr14:50463599
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.819+453C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463599 | ||||||
| chr14:50463660
|
G | T | 1 | a0007c0016t0011g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.819+392C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463660 | ||||||
| chr14:50463848
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.819+204C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463848 | ||||||
| chr14:50463867
|
G | C | 1 | a0001c0001t0001g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.819+185C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463867 | ||||||
| chr14:50463891
|
C | CA | 6 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(3): Show | 6 | HG00733.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.819+160dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463891 | ||||||
| chr14:50463891
|
C | CAAAAAAA others(5): Show |
1 | a0001c0006t0001g0233 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.819+149_819+160dup others(12): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463891 | ||||||
| chr14:50463891
|
C | CAAAAAAA others(8): Show |
1 | a0001c0006t0001g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.819+146_819+160dup others(15): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463891 | ||||||
| chr14:50463891
|
CA | C | 10 | a0001c0001t0001g0192a0001c0001t0001g0199a0001c0001t0001g0201others(7): Show | 10 | HG00423.hp2 HG02055.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.819+160delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463891 | ||||||
| chr14:50463891
|
CAA | C | 15 | a0001c0001t0001g0140a0001c0001t0001g0194a0001c0001t0001g0195others(12): Show | 15 | HG00140.hp1 HG00408.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.819+159_819+160del others(2): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463891 | ||||||
| chr14:50463891
|
CAAAAAAA others(1): Show |
C | 12 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(9): Show | 12 | HG01243.hp1 HG01261.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.819+153_819+160del others(8): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463891 | ||||||
| chr14:50463891
|
CAAAAAAA others(2): Show |
C | 45 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0031others(42): Show | 46 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.819+152_819+160del others(9): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463891 | ||||||
| chr14:50463891
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0001g0003a0001c0001t0001g0163a0001c0001t0001g0164others(2): Show | 6 | HG01255.hp1 HG01496.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+151_819+160del others(10): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463891 | ||||||
| chr14:50463891
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.819+150_819+160del others(11): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463891 | ||||||
| chr14:50463891
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.819+149_819+160del others(12): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463891 | ||||||
| chr14:50463891
|
CAAAAAAA others(7): Show |
C | 7 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0113others(4): Show | 7 | HG01433.hp1 HG02055.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+147_819+160del others(14): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463891 | ||||||
| chr14:50463891
|
CAAAAAAA others(8): Show |
C | 110 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0040others(107): Show | 112 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.819+146_819+160del others(15): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463891 | ||||||
| chr14:50463891
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0061 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.819+145_819+160del others(16): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463891 | ||||||
| chr14:50463891
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0003t0001g0005 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.819+144_819+160del others(17): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463891 | ||||||
| chr14:50463891
|
CAAAAAAA others(14): Show |
C | 6 | a0001c0001t0001g0180a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+140_819+160del others(21): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463891 | ||||||
| chr14:50463902
|
A | T | 1 | a0001c0001t0004g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.819+150T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463902 | ||||||
| chr14:50463908
|
A | T | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.819+144T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463908 | ||||||
| chr14:50463920
|
A | T | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.819+132T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 12/32 | chr14 | 50463920 | ||||||
| chr14:50464152
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.738-19C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50464152 | ||||||
| chr14:50464178
|
G | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(22): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.738-45C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50464178 | ||||||
| chr14:50464212
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.738-79G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50464212 | ||||||
| chr14:50464273
|
G | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.738-140C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50464273 | ||||||
| chr14:50464457
|
T | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.738-324A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50464457 | ||||||
| chr14:50464489
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0026 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.738-356A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50464489 | ||||||
| chr14:50464612
|
T | C | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.738-479A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50464612 | ||||||
| chr14:50464782
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.738-649G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50464782 | ||||||
| chr14:50464985
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0056 | 4 | HG01884.hp2 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-852G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50464985 | ||||||
| chr14:50465029
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.738-896C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50465029 | ||||||
| chr14:50465034
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.738-901T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50465034 | ||||||
| chr14:50465102
|
G | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 239 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.738-969C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50465102 | ||||||
| chr14:50465347
|
A | G | 3 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG01358.hp2 HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.738-1214T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50465347 | ||||||
| chr14:50465465
|
T | C | 14 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(11): Show | 15 | HG02055.hp2 HG02257.hp2 HG02896.hp2 others(12): Show |
intron_variant | MODIFIER | c.737+1118A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50465465 | ||||||
| chr14:50465539
|
C | T | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228 | 3 | HG03139.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.737+1044G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50465539 | ||||||
| chr14:50465718
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.737+865G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50465718 | ||||||
| chr14:50466013
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.737+570C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50466013 | ||||||
| chr14:50466075
|
C | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.737+508G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50466075 | ||||||
| chr14:50466129
|
T | G | 7 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0183others(4): Show | 7 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.737+454A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50466129 | ||||||
| chr14:50466194
|
T | C | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.737+389A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50466194 | ||||||
| chr14:50466381
|
C | CA | 75 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0035others(72): Show | 77 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.737+201dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50466381 | ||||||
| chr14:50466381
|
C | CAA | 27 | a0001c0001t0001g0101a0001c0001t0001g0112a0001c0001t0001g0140others(24): Show | 27 | HG00140.hp1 HG00408.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.737+200_737+201dup others(2): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50466381 | ||||||
| chr14:50466381
|
C | CAAA | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 6 | HG00423.hp2 HG01261.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.737+199_737+201dup others(3): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50466381 | ||||||
| chr14:50466381
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.737+192_737+201del others(10): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 11/32 | chr14 | 50466381 | ||||||
| chr14:50467054
|
G | T | 1 | a0001c0001t0003g0108 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.675-409C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 10/32 | chr14 | 50467054 | ||||||
| chr14:50467073
|
T | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0056 | 4 | HG01884.hp2 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.675-428A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 10/32 | chr14 | 50467073 | ||||||
| chr14:50467196
|
T | C | 1 | a0001c0006t0001g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.675-551A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 10/32 | chr14 | 50467196 | ||||||
| chr14:50467487
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.675-842T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 10/32 | chr14 | 50467487 | ||||||
| chr14:50467755
|
T | G | 1 | a0001c0001t0001g0138 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.674+896A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 10/32 | chr14 | 50467755 | ||||||
| chr14:50468119
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.674+532A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 10/32 | chr14 | 50468119 | ||||||
| chr14:50468121
|
A | T | 1 | a0001c0001t0003g0159 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.674+530T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 10/32 | chr14 | 50468121 | ||||||
| chr14:50468160
|
C | T | 8 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(5): Show | 8 | HG02257.hp2 HG02922.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.674+491G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 10/32 | chr14 | 50468160 | ||||||
| chr14:50468204
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.674+447G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 10/32 | chr14 | 50468204 | ||||||
| chr14:50468227
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.674+424A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 10/32 | chr14 | 50468227 | ||||||
| chr14:50468335
|
G | C | 3 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG01358.hp2 HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.674+316C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 10/32 | chr14 | 50468335 | ||||||
| chr14:50468379
|
A | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(10): Show | 14 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.674+272T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 10/32 | chr14 | 50468379 | ||||||
| chr14:50468432
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 199 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.674+219T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 10/32 | chr14 | 50468432 | ||||||
| chr14:50468872
|
G | T | 1 | a0001c0001t0001g0194 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.543-90C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50468872 | ||||||
| chr14:50468898
|
G | T | 1 | a0001c0001t0001g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.543-116C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50468898 | ||||||
| chr14:50468974
|
A | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0056 | 4 | HG01884.hp2 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-192T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50468974 | ||||||
| chr14:50469002
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.543-220A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50469002 | ||||||
| chr14:50469219
|
C | T | 2 | a0001c0014t0001g0218a0007c0016t0011g0222 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.543-437G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50469219 | ||||||
| chr14:50469354
|
C | T | 8 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(5): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.543-572G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50469354 | ||||||
| chr14:50469526
|
A | T | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.543-744T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50469526 | ||||||
| chr14:50469625
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.543-843T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50469625 | ||||||
| chr14:50469692
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0056 | 4 | HG01884.hp2 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-910C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50469692 | ||||||
| chr14:50469706
|
A | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(22): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.543-924T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50469706 | ||||||
| chr14:50469835
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0210 | 3 | HG01069.hp1 HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.543-1053A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50469835 | ||||||
| chr14:50469867
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.543-1085A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50469867 | ||||||
| chr14:50469893
|
T | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(22): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.543-1111A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50469893 | ||||||
| chr14:50470014
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.543-1232T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50470014 | ||||||
| chr14:50470243
|
A | C | 7 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG01169.hp2 HG01928.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.543-1461T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50470243 | ||||||
| chr14:50470463
|
T | C | 7 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0183others(4): Show | 7 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.543-1681A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50470463 | ||||||
| chr14:50470653
|
T | TAC | 3 | a0001c0001t0001g0194a0001c0001t0001g0209a0001c0001t0001g0224 | 3 | HG02280.hp2 HG06807.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.543-1873_543-1872d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50470653 | ||||||
| chr14:50470653
|
TAC | T | 8 | a0001c0001t0001g0201a0001c0001t0001g0214a0001c0007t0001g0215others(5): Show | 8 | HG00423.hp2 HG02257.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.543-1873_543-1872d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50470653 | ||||||
| chr14:50470653
|
TACAC | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(18): Show | 22 | HG01261.hp2 HG01361.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.543-1875_543-1872d others(6): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50470653 | ||||||
| chr14:50470653
|
TACACAC | T | 44 | a0001c0001t0001g0038a0001c0001t0001g0057a0001c0001t0001g0113others(41): Show | 45 | HG00738.hp1 HG01192.hp1 HG01952.hp2 others(42): Show |
intron_variant | MODIFIER | c.543-1877_543-1872d others(8): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50470653 | ||||||
| chr14:50470653
|
TACACACA others(1): Show |
T | 128 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0041others(125): Show | 130 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.543-1879_543-1872d others(10): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50470653 | ||||||
| chr14:50470653
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0003a0001c0001t0001g0167 | 3 | HG01255.hp1 HG01496.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.543-1881_543-1872d others(12): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50470653 | ||||||
| chr14:50470792
|
A | C | 2 | a0001c0006t0001g0232a0001c0006t0001g0233 | 2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.543-2010T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50470792 | ||||||
| chr14:50470972
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0056 | 4 | HG01884.hp2 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.543-2190T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50470972 | ||||||
| chr14:50471019
|
T | A | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.543-2237A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50471019 | ||||||
| chr14:50471067
|
C | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0170 | 3 | HG00735.hp2 HG01256.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.543-2285G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50471067 | ||||||
| chr14:50471175
|
C | T | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.543-2393G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50471175 | ||||||
| chr14:50471311
|
A | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.543-2529T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50471311 | ||||||
| chr14:50471851
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.543-3069C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50471851 | ||||||
| chr14:50472159
|
TA | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(48): Show | 53 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.542+2917delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50472159 | ||||||
| chr14:50472159
|
TAA | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0225a0001c0001t0001g0226others(3): Show | 6 | HG02976.hp2 HG03139.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.542+2916_542+2917d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50472159 | ||||||
| chr14:50472160
|
A | T | 3 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217 | 3 | HG02257.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.542+2917T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50472160 | ||||||
| chr14:50472294
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.542+2783C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50472294 | ||||||
| chr14:50472312
|
T | C | 1 | a0001c0004t0001g0093 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.542+2765A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50472312 | ||||||
| chr14:50472314
|
C | A | 2 | a0001c0006t0001g0232a0001c0006t0001g0233 | 2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.542+2763G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50472314 | ||||||
| chr14:50472338
|
A | C | 1 | a0001c0001t0001g0141 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.542+2739T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50472338 | ||||||
| chr14:50472442
|
G | T | 1 | a0002c0002t0001g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.542+2635C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50472442 | ||||||
| chr14:50472456
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.542+2621G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50472456 | ||||||
| chr14:50472490
|
A | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(158): Show | 164 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.542+2587T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50472490 | ||||||
| chr14:50472738
|
A | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.542+2339T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50472738 | ||||||
| chr14:50472923
|
T | C | 6 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0077others(3): Show | 6 | HG01433.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.542+2154A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50472923 | ||||||
| chr14:50472931
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.542+2146T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50472931 | ||||||
| chr14:50473045
|
T | C | 1 | a0001c0001t0002g0007 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.542+2032A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50473045 | ||||||
| chr14:50473048
|
T | C | 7 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(4): Show | 7 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.542+2029A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50473048 | ||||||
| chr14:50473068
|
T | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.542+2009A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50473068 | ||||||
| chr14:50473181
|
T | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0115others(41): Show | 45 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.542+1896A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50473181 | ||||||
| chr14:50473268
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.542+1809C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50473268 | ||||||
| chr14:50473716
|
C | CT | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(109): Show | 116 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.542+1360dupA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50473716 | ||||||
| chr14:50473716
|
C | CTT | 20 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0053others(17): Show | 20 | HG00423.hp1 HG00733.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.542+1359_542+1360d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50473716 | ||||||
| chr14:50473716
|
C | CTTT | 8 | a0001c0001t0001g0214a0001c0003t0001g0005a0001c0003t0001g0219others(5): Show | 9 | HG02055.hp2 HG02647.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.542+1358_542+1360d others(5): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50473716 | ||||||
| chr14:50473716
|
CTTTTTTT others(1): Show |
C | 44 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0115others(41): Show | 45 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.542+1353_542+1360d others(10): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50473716 | ||||||
| chr14:50473877
|
C | T | 1 | a0002c0002t0001g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.542+1200G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50473877 | ||||||
| chr14:50473884
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 118 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.542+1193G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50473884 | ||||||
| chr14:50474055
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.542+1022C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50474055 | ||||||
| chr14:50474119
|
T | C | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.542+958A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50474119 | ||||||
| chr14:50474180
|
T | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(158): Show | 164 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.542+897A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50474180 | ||||||
| chr14:50474380
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.542+697G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50474380 | ||||||
| chr14:50474568
|
TG | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0115others(41): Show | 45 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.542+508delC | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50474568 | ||||||
| chr14:50474926
|
G | C | 7 | a0001c0001t0001g0075a0001c0004t0001g0081a0002c0002t0001g0051others(4): Show | 7 | HG00741.hp2 HG01071.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.542+151C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50474926 | ||||||
| chr14:50474968
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0210 | 3 | HG01069.hp1 HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.542+109G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 9/32 | chr14 | 50474968 | ||||||
| chr14:50475266
|
G | A | 2 | a0001c0014t0001g0218a0007c0016t0011g0222 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.470-117C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 8/32 | chr14 | 50475266 | ||||||
| chr14:50475329
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 197 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.470-180G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 8/32 | chr14 | 50475329 | ||||||
| chr14:50475435
|
GCACAAAA others(7): Show |
G | 1 | a0001c0001t0001g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.470-300_470-287del others(14): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 8/32 | chr14 | 50475435 | ||||||
| chr14:50475460
|
A | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02523.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.470-311T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 8/32 | chr14 | 50475460 | ||||||
| chr14:50475592
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.470-443A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 8/32 | chr14 | 50475592 | ||||||
| chr14:50475595
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.470-446A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 8/32 | chr14 | 50475595 | ||||||
| chr14:50475689
|
A | G | 1 | a0001c0003t0001g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.469+439T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 8/32 | chr14 | 50475689 | ||||||
| chr14:50475914
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.469+214C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 8/32 | chr14 | 50475914 | ||||||
| chr14:50476249
|
A | T | 1 | a0001c0006t0010g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.426+10T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 7/32 | chr14 | 50476249 | ||||||
| chr14:50476316
|
T | TA | 44 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0026others(41): Show | 45 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.379-11dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50476316 | ||||||
| chr14:50476355
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.379-49A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50476355 | ||||||
| chr14:50476363
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.379-57G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50476363 | ||||||
| chr14:50476364
|
T | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(22): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.379-58A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50476364 | ||||||
| chr14:50476423
|
A | G | 1 | a0001c0001t0006g0006 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.379-117T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50476423 | ||||||
| chr14:50476650
|
C | T | 1 | a0001c0014t0001g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.379-344G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50476650 | ||||||
| chr14:50476708
|
C | T | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG00733.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.379-402G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50476708 | ||||||
| chr14:50477119
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.379-813A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50477119 | ||||||
| chr14:50477347
|
T | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080 | 3 | HG01433.hp2 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.379-1041A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50477347 | ||||||
| chr14:50477678
|
T | A | 1 | a0001c0001t0001g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.379-1372A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50477678 | ||||||
| chr14:50477695
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.379-1389C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50477695 | ||||||
| chr14:50477696
|
G | C | 1 | a0002c0002t0001g0076 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.379-1390C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50477696 | ||||||
| chr14:50477791
|
T | C | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.379-1485A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50477791 | ||||||
| chr14:50477984
|
T | G | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.379-1678A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50477984 | ||||||
| chr14:50478085
|
G | A | 1 | a0007c0016t0011g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.379-1779C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50478085 | ||||||
| chr14:50478110
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0041others(117): Show | 122 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.379-1804A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50478110 | ||||||
| chr14:50478217
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.379-1911A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50478217 | ||||||
| chr14:50478281
|
TTC | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(161): Show | 167 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.379-1977_379-1976d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50478281 | ||||||
| chr14:50478334
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(161): Show | 167 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.379-2028A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50478334 | ||||||
| chr14:50478660
|
A | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0097 | 2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.379-2354T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50478660 | ||||||
| chr14:50478728
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.379-2422C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50478728 | ||||||
| chr14:50478996
|
G | GT | 14 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(11): Show | 14 | HG01358.hp2 HG01361.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.379-2691dupA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50478996 | ||||||
| chr14:50479003
|
TCG | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 189 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.379-2699_379-2698d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479003 | ||||||
| chr14:50479005
|
G | GT | 4 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(1): Show | 5 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-2700dupA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479005 | ||||||
| chr14:50479005
|
G | T | 1 | a0001c0001t0001g0085 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.379-2699C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479005 | ||||||
| chr14:50479005
|
GTT | G | 10 | a0001c0001t0001g0052a0001c0001t0001g0132a0001c0001t0001g0171others(7): Show | 10 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.379-2701_379-2700d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479005 | ||||||
| chr14:50479007
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 190 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.379-2701A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479007 | ||||||
| chr14:50479008
|
T | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 190 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.379-2702A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479008 | ||||||
| chr14:50479017
|
T | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 204 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.379-2711A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479017 | ||||||
| chr14:50479032
|
T | G | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.379-2726A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479032 | ||||||
| chr14:50479117
|
TC | T | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG00733.hp2 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-2812delG | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479117 | ||||||
| chr14:50479156
|
C | T | 1 | a0002c0002t0001g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.379-2850G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479156 | ||||||
| chr14:50479186
|
C | CT | 163 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(160): Show | 166 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.379-2881dupA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479186 | ||||||
| chr14:50479186
|
CT | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(27): Show | 31 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.379-2881delA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479186 | ||||||
| chr14:50479375
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.378+2986C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479375 | ||||||
| chr14:50479412
|
TTTG | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(22): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.378+2946_378+2948d others(5): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479412 | ||||||
| chr14:50479416
|
T | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(161): Show | 167 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.378+2945A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479416 | ||||||
| chr14:50479444
|
CATCCTTT others(5): Show |
C | 3 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217 | 3 | HG02257.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.378+2905_378+2916d others(14): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479444 | ||||||
| chr14:50479919
|
T | G | 32 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(29): Show | 33 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.378+2442A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50479919 | ||||||
| chr14:50480015
|
CT | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 18 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.378+2345delA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480015 | ||||||
| chr14:50480018
|
C | G | 17 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 18 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.378+2343G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480018 | ||||||
| chr14:50480030
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.378+2331C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480030 | ||||||
| chr14:50480132
|
G | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(28): Show | 32 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.378+2229C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480132 | ||||||
| chr14:50480158
|
G | T | 6 | a0001c0001t0001g0180a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+2203C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480158 | ||||||
| chr14:50480403
|
C | CT | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(169): Show | 175 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.378+1957dupA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480403 | ||||||
| chr14:50480412
|
T | A | 6 | a0001c0001t0001g0180a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+1949A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480412 | ||||||
| chr14:50480447
|
C | T | 3 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217 | 3 | HG02257.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.378+1914G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480447 | ||||||
| chr14:50480575
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02145.hp2 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.378+1786C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480575 | ||||||
| chr14:50480660
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0041others(116): Show | 121 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.378+1701G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480660 | ||||||
| chr14:50480754
|
A | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(161): Show | 167 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.378+1607T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480754 | ||||||
| chr14:50480824
|
A | C | 1 | a0001c0001t0003g0108 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.378+1537T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480824 | ||||||
| chr14:50480830
|
G | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 200 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.378+1531C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480830 | ||||||
| chr14:50480895
|
T | C | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.378+1466A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480895 | ||||||
| chr14:50480929
|
C | A | 1 | a0001c0001t0003g0105 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.378+1432G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480929 | ||||||
| chr14:50480980
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.378+1381G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50480980 | ||||||
| chr14:50481147
|
G | GA | 5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(2): Show | 5 | HG01261.hp2 HG01496.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+1213dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50481147 | ||||||
| chr14:50481266
|
C | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(158): Show | 164 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.378+1095G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50481266 | ||||||
| chr14:50481292
|
C | A | 8 | a0001c0001t0001g0075a0001c0004t0001g0081a0002c0002t0001g0051others(5): Show | 8 | HG00741.hp2 HG01071.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.378+1069G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50481292 | ||||||
| chr14:50481294
|
A | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 9 | HG00738.hp1 HG01255.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+1067T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50481294 | ||||||
| chr14:50481296
|
A | C | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.378+1065T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50481296 | ||||||
| chr14:50481305
|
T | A | 15 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 16 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.378+1056A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50481305 | ||||||
| chr14:50481368
|
T | C | 6 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+993A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50481368 | ||||||
| chr14:50481543
|
A | G | 1 | a0001c0001t0003g0159 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.378+818T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50481543 | ||||||
| chr14:50481596
|
C | T | 1 | a0007c0016t0011g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.378+765G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50481596 | ||||||
| chr14:50481601
|
A | T | 6 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG03139.hp1 HG03579.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+760T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50481601 | ||||||
| chr14:50481697
|
A | C | 1 | a0001c0001t0001g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.378+664T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50481697 | ||||||
| chr14:50481835
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.378+526T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50481835 | ||||||
| chr14:50482000
|
A | G | 8 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(5): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.378+361T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50482000 | ||||||
| chr14:50482067
|
G | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 234 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.378+294C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50482067 | ||||||
| chr14:50482152
|
A | G | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.378+209T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50482152 | ||||||
| chr14:50482222
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.378+139T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50482222 | ||||||
| chr14:50482289
|
T | C | 3 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217 | 3 | HG02257.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.378+72A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 6/32 | chr14 | 50482289 | ||||||
| chr14:50482478
|
TA | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.323-63delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50482478 | ||||||
| chr14:50482503
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(28): Show | 32 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.323-87C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50482503 | ||||||
| chr14:50482553
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0026 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.323-137G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50482553 | ||||||
| chr14:50482668
|
T | G | 60 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(57): Show | 61 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.323-252A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50482668 | ||||||
| chr14:50482690
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 9 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.323-274A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50482690 | ||||||
| chr14:50482762
|
C | T | 11 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(8): Show | 12 | HG00733.hp2 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.323-346G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50482762 | ||||||
| chr14:50482835
|
T | C | 11 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(8): Show | 12 | HG00733.hp2 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.323-419A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50482835 | ||||||
| chr14:50483021
|
T | C | 2 | a0005c0010t0001g0063a0005c0010t0001g0064 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.323-605A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50483021 | ||||||
| chr14:50483218
|
A | C | 1 | a0001c0001t0001g0166 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.323-802T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50483218 | ||||||
| chr14:50483224
|
T | C | 1 | a0001c0014t0001g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.323-808A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50483224 | ||||||
| chr14:50483254
|
T | C | 2 | a0001c0006t0001g0232a0001c0006t0001g0233 | 2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.323-838A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50483254 | ||||||
| chr14:50483349
|
G | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(29): Show | 33 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.323-933C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50483349 | ||||||
| chr14:50483725
|
C | CA | 8 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0038others(5): Show | 8 | HG00423.hp1 HG00738.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.323-1310dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50483725 | ||||||
| chr14:50483725
|
CA | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(19): Show | 23 | HG00733.hp2 HG01123.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.323-1310delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50483725 | ||||||
| chr14:50483837
|
C | CATTT | 7 | a0001c0001t0001g0123a0001c0001t0001g0180a0001c0001t0001g0184others(4): Show | 7 | HG01361.hp1 HG02896.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.323-1425_323-1422d others(6): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50483837 | ||||||
| chr14:50483837
|
CATTT | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0025others(118): Show | 123 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(120): Show |
intron_variant | MODIFIER | c.323-1425_323-1422d others(6): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50483837 | ||||||
| chr14:50483837
|
CATTTATT others(1): Show |
C | 23 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0026others(20): Show | 24 | HG00733.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.323-1429_323-1422d others(10): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50483837 | ||||||
| chr14:50484442
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.322+1136G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50484442 | ||||||
| chr14:50484488
|
T | A | 5 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217others(2): Show | 5 | HG02257.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.322+1090A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50484488 | ||||||
| chr14:50484489
|
A | G | 4 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0116others(1): Show | 4 | HG02027.hp1 NA19056.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.322+1089T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50484489 | ||||||
| chr14:50484638
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0002g0016 | 2 | HG01433.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.322+940C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50484638 | ||||||
| chr14:50484659
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.322+919G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50484659 | ||||||
| chr14:50484691
|
T | A | 2 | a0001c0001t0001g0075a0002c0002t0001g0051 | 2 | HG01258.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.322+887A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50484691 | ||||||
| chr14:50484708
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 18 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.322+870C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50484708 | ||||||
| chr14:50484722
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.322+856G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50484722 | ||||||
| chr14:50484770
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.322+808A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50484770 | ||||||
| chr14:50484937
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.322+641G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50484937 | ||||||
| chr14:50485062
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.322+516T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50485062 | ||||||
| chr14:50485085
|
A | T | 6 | a0001c0001t0001g0180a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.322+493T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50485085 | ||||||
| chr14:50485088
|
C | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.322+490G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50485088 | ||||||
| chr14:50485130
|
T | A | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.322+448A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50485130 | ||||||
| chr14:50485211
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01261.hp2 HG01496.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.322+367A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50485211 | ||||||
| chr14:50485284
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.322+294A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50485284 | ||||||
| chr14:50485332
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.322+246G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50485332 | ||||||
| chr14:50485458
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.322+120C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 5/32 | chr14 | 50485458 | ||||||
| chr14:50485649
|
C | T | 6 | a0001c0001t0001g0180a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.258-7G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 4/32 | chr14 | 50485649 | ||||||
| chr14:50485676
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 9 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.258-34T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 4/32 | chr14 | 50485676 | ||||||
| chr14:50485960
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0167 | 3 | HG01255.hp1 HG01496.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.257+144A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 4/32 | chr14 | 50485960 | ||||||
| chr14:50486208
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0210 | 3 | HG01069.hp1 HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.167-14A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50486208 | ||||||
| chr14:50486554
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01261.hp2 HG01496.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.167-360A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50486554 | ||||||
| chr14:50486913
|
T | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(22): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.167-719A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50486913 | ||||||
| chr14:50487293
|
C | T | 7 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0183others(4): Show | 7 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.167-1099G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50487293 | ||||||
| chr14:50487294
|
G | A | 12 | a0001c0001t0001g0095a0001c0001t0001g0101a0001c0001t0001g0106others(9): Show | 12 | HG00408.hp1 NA18939.hp1 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.167-1100C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50487294 | ||||||
| chr14:50487372
|
TATA | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(111): Show | 117 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(114): Show |
intron_variant | MODIFIER | c.167-1181_167-1179d others(5): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50487372 | ||||||
| chr14:50487408
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.167-1214C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50487408 | ||||||
| chr14:50487412
|
A | C | 11 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(8): Show | 11 | HG01123.hp2 HG01169.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.167-1218T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50487412 | ||||||
| chr14:50487563
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0034others(2): Show | 5 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.167-1369C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50487563 | ||||||
| chr14:50487585
|
T | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(10): Show | 14 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.167-1391A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50487585 | ||||||
| chr14:50487595
|
A | G | 1 | a0001c0001t0002g0018 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.167-1401T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50487595 | ||||||
| chr14:50487621
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(22): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.167-1427G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50487621 | ||||||
| chr14:50487845
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.167-1651T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50487845 | ||||||
| chr14:50487953
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.167-1759T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50487953 | ||||||
| chr14:50488168
|
C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0023others(63): Show | 69 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.167-1974G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50488168 | ||||||
| chr14:50488371
|
C | A | 4 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217others(1): Show | 4 | HG02257.hp2 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.167-2177G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50488371 | ||||||
| chr14:50488479
|
A | G | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG01123.hp2 HG02015.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.167-2285T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50488479 | ||||||
| chr14:50488736
|
T | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG00733.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.167-2542A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50488736 | ||||||
| chr14:50489031
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.167-2837G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50489031 | ||||||
| chr14:50489252
|
G | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(32): Show | 37 | HG00733.hp2 HG01256.hp2 HG01258.hp2 others(34): Show |
intron_variant | MODIFIER | c.167-3058C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50489252 | ||||||
| chr14:50489542
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.167-3348A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50489542 | ||||||
| chr14:50489841
|
C | G | 15 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(12): Show | 15 | HG00408.hp2 HG00423.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.167-3647G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50489841 | ||||||
| chr14:50489894
|
C | T | 1 | a0004c0008t0001g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.167-3700G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50489894 | ||||||
| chr14:50490090
|
A | T | 1 | a0007c0016t0011g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.167-3896T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490090 | ||||||
| chr14:50490130
|
A | AGT | 61 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(58): Show | 61 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.167-3938_167-3937d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490130 | ||||||
| chr14:50490130
|
A | AGTGT | 13 | a0001c0001t0001g0052a0001c0001t0001g0115a0001c0001t0001g0225others(10): Show | 14 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.167-3940_167-3937d others(6): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490130 | ||||||
| chr14:50490130
|
A | AGTGTGTG others(10): Show |
1 | a0001c0001t0003g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.167-3937_167-3936i others(19): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490130 | ||||||
| chr14:50490130
|
A | T | 1 | a0001c0001t0001g0095 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.167-3936T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490130 | ||||||
| chr14:50490130
|
AGT | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0056a0001c0001t0001g0075others(41): Show | 46 | HG00140.hp2 HG00738.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.167-3938_167-3937d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490130 | ||||||
| chr14:50490132
|
T | A | 1 | a0001c0001t0001g0119 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.167-3938A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490132 | ||||||
| chr14:50490159
|
G | A | 1 | a0001c0001t0003g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.167-3965C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490159 | ||||||
| chr14:50490159
|
G | GTA | 10 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(7): Show | 11 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.167-3967_167-3966d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490159 | ||||||
| chr14:50490159
|
G | GTGTA | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01261.hp2 HG01496.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.167-3966_167-3965i others(6): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490159 | ||||||
| chr14:50490159
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0001g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.167-3966_167-3965i others(12): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490159 | ||||||
| chr14:50490159
|
G | GTGTGTGT others(7): Show |
7 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(4): Show | 7 | HG01358.hp2 HG01433.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.167-3966_167-3965i others(16): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490159 | ||||||
| chr14:50490159
|
G | GTGTGTGT others(11): Show |
1 | a0001c0001t0001g0084 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.167-3966_167-3965i others(20): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490159 | ||||||
| chr14:50490159
|
G | GTGTGTGT others(9): Show |
25 | a0001c0001t0001g0023a0001c0001t0001g0058a0001c0001t0001g0060others(22): Show | 25 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.167-3966_167-3965i others(18): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490159 | ||||||
| chr14:50490159
|
G | GTGTGTGT others(11): Show |
7 | a0001c0001t0001g0059a0001c0001t0001g0096a0001c0001t0001g0097others(4): Show | 7 | HG01243.hp2 HG01934.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.167-3966_167-3965i others(20): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490159 | ||||||
| chr14:50490159
|
G | GTGTGTGT others(13): Show |
6 | a0001c0001t0001g0026a0001c0001t0001g0089a0001c0001t0001g0116others(3): Show | 6 | HG02027.hp1 HG02258.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.167-3966_167-3965i others(22): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490159 | ||||||
| chr14:50490159
|
G | GTGTGTGT others(15): Show |
1 | a0001c0001t0001g0085 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.167-3966_167-3965i others(24): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490159 | ||||||
| chr14:50490186
|
GA | G | 10 | a0001c0001t0001g0075a0001c0001t0006g0006a0001c0003t0001g0221others(7): Show | 10 | HG00741.hp2 HG01071.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.167-3993delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490186 | ||||||
| chr14:50490256
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.167-4062C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490256 | ||||||
| chr14:50490266
|
C | G | 5 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217others(2): Show | 5 | HG02257.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.167-4072G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490266 | ||||||
| chr14:50490276
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.167-4082A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490276 | ||||||
| chr14:50490423
|
T | C | 1 | a0005c0010t0001g0064 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.167-4229A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490423 | ||||||
| chr14:50490537
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.167-4343C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490537 | ||||||
| chr14:50490641
|
A | G | 1 | a0001c0003t0001g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.167-4447T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490641 | ||||||
| chr14:50490648
|
T | A | 1 | a0001c0001t0001g0001 | 3 | HG02559.hp1 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.167-4454A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490648 | ||||||
| chr14:50490662
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.167-4468C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490662 | ||||||
| chr14:50490975
|
TA | T | 3 | a0001c0001t0001g0134a0001c0001t0003g0131a0001c0001t0012g0179 | 3 | NA18955.hp1 NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.167-4782delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50490975 | ||||||
| chr14:50491166
|
C | A | 7 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0007t0001g0215others(4): Show | 7 | HG02257.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.167-4972G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50491166 | ||||||
| chr14:50491324
|
C | CT | 8 | a0001c0001t0001g0070a0001c0001t0001g0115a0001c0001t0001g0132others(5): Show | 8 | HG00733.hp2 HG01169.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.167-5131dupA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50491324 | ||||||
| chr14:50491324
|
CT | C | 7 | a0001c0001t0001g0028a0001c0001t0001g0075a0001c0001t0001g0206others(4): Show | 7 | HG01258.hp1 HG01346.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.167-5131delA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50491324 | ||||||
| chr14:50491377
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.167-5183G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50491377 | ||||||
| chr14:50491398
|
C | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.167-5204G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50491398 | ||||||
| chr14:50491527
|
C | T | 36 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(33): Show | 36 | HG00140.hp2 HG00738.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.167-5333G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50491527 | ||||||
| chr14:50491538
|
C | A | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(4): Show | 7 | HG00733.hp1 HG00735.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.167-5344G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50491538 | ||||||
| chr14:50491687
|
CT | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(13): Show | 17 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.167-5494delA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50491687 | ||||||
| chr14:50491702
|
T | C | 1 | a0001c0001t0001g0202 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.167-5508A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50491702 | ||||||
| chr14:50491703
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.167-5509G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50491703 | ||||||
| chr14:50491704
|
G | A | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228 | 3 | HG03139.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.167-5510C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50491704 | ||||||
| chr14:50491720
|
G | C | 70 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0023others(67): Show | 73 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.167-5526C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50491720 | ||||||
| chr14:50491800
|
C | A | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.167-5606G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50491800 | ||||||
| chr14:50491879
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.167-5685C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50491879 | ||||||
| chr14:50492137
|
G | A | 69 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0023others(66): Show | 72 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.167-5943C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50492137 | ||||||
| chr14:50492428
|
C | CA | 10 | a0001c0001t0001g0088a0001c0001t0001g0154a0001c0001t0001g0225others(7): Show | 11 | HG01192.hp1 HG02055.hp2 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.167-6235dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50492428 | ||||||
| chr14:50492591
|
CA | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 191 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.167-6398delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50492591 | ||||||
| chr14:50492591
|
CAA | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0040a0001c0001t0001g0140others(39): Show | 44 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.167-6399_167-6398d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50492591 | ||||||
| chr14:50492716
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.167-6522G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50492716 | ||||||
| chr14:50493126
|
A | G | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0078others(2): Show | 5 | HG01433.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.167-6932T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50493126 | ||||||
| chr14:50493226
|
G | A | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG00733.hp2 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.167-7032C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50493226 | ||||||
| chr14:50493237
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.167-7043G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50493237 | ||||||
| chr14:50493353
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0056a0001c0001t0001g0077others(1): Show | 6 | HG01884.hp2 HG02559.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.167-7159A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50493353 | ||||||
| chr14:50493452
|
C | A | 1 | a0002c0002t0001g0074 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.167-7258G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50493452 | ||||||
| chr14:50493726
|
G | A | 31 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(28): Show | 31 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.167-7532C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50493726 | ||||||
| chr14:50493742
|
G | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(54): Show | 58 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.167-7548C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50493742 | ||||||
| chr14:50493987
|
C | CA | 6 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0114others(3): Show | 6 | HG01261.hp1 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.167-7794dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50493987 | ||||||
| chr14:50494178
|
A | T | 1 | a0007c0016t0011g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.167-7984T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50494178 | ||||||
| chr14:50494200
|
G | A | 2 | a0004c0008t0001g0039a0004c0008t0001g0109 | 2 | HG02258.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.167-8006C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50494200 | ||||||
| chr14:50494261
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.167-8067C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50494261 | ||||||
| chr14:50494294
|
G | A | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.167-8100C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50494294 | ||||||
| chr14:50494538
|
C | A | 1 | a0001c0014t0001g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.167-8344G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50494538 | ||||||
| chr14:50494754
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.167-8560C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50494754 | ||||||
| chr14:50494868
|
C | T | 2 | a0005c0010t0001g0063a0005c0010t0001g0064 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.167-8674G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50494868 | ||||||
| chr14:50494901
|
C | T | 1 | a0001c0013t0001g0193 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.167-8707G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50494901 | ||||||
| chr14:50494963
|
A | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(28): Show | 32 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.167-8769T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50494963 | ||||||
| chr14:50494964
|
T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 230 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.167-8770A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50494964 | ||||||
| chr14:50495178
|
G | C | 2 | a0001c0004t0001g0081a0002c0002t0007g0037 | 2 | HG01071.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.167-8984C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50495178 | ||||||
| chr14:50495359
|
C | T | 1 | a0001c0001t0003g0159 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.167-9165G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50495359 | ||||||
| chr14:50495431
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.167-9237C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50495431 | ||||||
| chr14:50495596
|
G | A | 1 | a0001c0014t0001g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.166+9204C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50495596 | ||||||
| chr14:50495638
|
T | C | 4 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(1): Show | 5 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.166+9162A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50495638 | ||||||
| chr14:50495826
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.166+8974A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50495826 | ||||||
| chr14:50495993
|
C | T | 1 | a0001c0014t0001g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.166+8807G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50495993 | ||||||
| chr14:50496250
|
C | T | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0078others(2): Show | 5 | HG01433.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.166+8550G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50496250 | ||||||
| chr14:50496255
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.166+8545C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50496255 | ||||||
| chr14:50496289
|
G | A | 1 | a0001c0004t0001g0111 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.166+8511C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50496289 | ||||||
| chr14:50496402
|
T | C | 32 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(29): Show | 33 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.166+8398A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50496402 | ||||||
| chr14:50496562
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.166+8238C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50496562 | ||||||
| chr14:50496577
|
T | G | 7 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0183others(4): Show | 7 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.166+8223A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50496577 | ||||||
| chr14:50496611
|
T | G | 1 | a0001c0001t0001g0080 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.166+8189A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50496611 | ||||||
| chr14:50496815
|
A | AAAAAAT | 8 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(5): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.166+7979_166+7984d others(8): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50496815 | ||||||
| chr14:50496896
|
T | C | 1 | a0001c0001t0003g0110 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.166+7904A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50496896 | ||||||
| chr14:50496903
|
T | A | 16 | a0001c0001t0001g0140a0001c0001t0001g0194a0001c0001t0001g0195others(13): Show | 16 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(13): Show |
intron_variant | MODIFIER | c.166+7897A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50496903 | ||||||
| chr14:50497013
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.166+7787A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50497013 | ||||||
| chr14:50497179
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.166+7621C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50497179 | ||||||
| chr14:50497200
|
CATA | C | 12 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0053others(9): Show | 12 | HG01069.hp2 HG01074.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.166+7597_166+7599d others(5): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50497200 | ||||||
| chr14:50497335
|
G | A | 1 | a0001c0004t0001g0081 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.166+7465C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50497335 | ||||||
| chr14:50497520
|
T | TTGGCCAT others(11): Show |
1 | a0001c0001t0001g0139 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.166+7279_166+7280i others(20): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50497520 | ||||||
| chr14:50497540
|
G | T | 1 | a0001c0001t0001g0139 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.166+7260C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50497540 | ||||||
| chr14:50497582
|
G | T | 1 | a0001c0001t0001g0139 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.166+7218C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50497582 | ||||||
| chr14:50497646
|
C | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 9 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.166+7154G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50497646 | ||||||
| chr14:50497681
|
T | A | 1 | a0001c0001t0001g0139 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.166+7119A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50497681 | ||||||
| chr14:50497701
|
G | T | 1 | a0001c0001t0001g0139 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.166+7099C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50497701 | ||||||
| chr14:50497718
|
A | G | 4 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217others(1): Show | 4 | HG02257.hp2 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.166+7082T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50497718 | ||||||
| chr14:50497844
|
G | T | 1 | a0001c0001t0001g0139 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.166+6956C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50497844 | ||||||
| chr14:50497903
|
C | A | 1 | a0001c0001t0001g0139 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.166+6897G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50497903 | ||||||
| chr14:50498446
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.166+6354C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50498446 | ||||||
| chr14:50498478
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.166+6322T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50498478 | ||||||
| chr14:50498715
|
G | A | 3 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217 | 3 | HG02257.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.166+6085C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50498715 | ||||||
| chr14:50498727
|
G | A | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00140.hp2 HG00738.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.166+6073C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50498727 | ||||||
| chr14:50498776
|
A | G | 8 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(5): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.166+6024T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50498776 | ||||||
| chr14:50498816
|
T | A | 1 | a0001c0001t0001g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.166+5984A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50498816 | ||||||
| chr14:50498864
|
A | G | 1 | a0002c0002t0001g0051 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.166+5936T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50498864 | ||||||
| chr14:50499324
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(61): Show | 65 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.166+5476A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50499324 | ||||||
| chr14:50499332
|
T | C | 1 | a0007c0016t0011g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.166+5468A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50499332 | ||||||
| chr14:50499453
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0113 | 2 | NA18988.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.166+5347A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50499453 | ||||||
| chr14:50499484
|
T | A | 8 | a0001c0001t0001g0075a0001c0004t0001g0081a0002c0002t0001g0051others(5): Show | 8 | HG00741.hp2 HG01071.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.166+5316A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50499484 | ||||||
| chr14:50499593
|
G | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(7): Show | 11 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.166+5207C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50499593 | ||||||
| chr14:50499608
|
A | C | 1 | a0001c0001t0002g0019 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.166+5192T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50499608 | ||||||
| chr14:50499656
|
T | TA | 6 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0012g0179others(3): Show | 6 | HG00741.hp1 HG01981.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.166+5143dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50499656 | ||||||
| chr14:50499981
|
G | A | 1 | a0001c0014t0001g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.166+4819C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50499981 | ||||||
| chr14:50500027
|
G | A | 34 | a0001c0001t0001g0060a0001c0001t0001g0084a0001c0001t0001g0085others(31): Show | 34 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.166+4773C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50500027 | ||||||
| chr14:50500102
|
C | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(222): Show | 231 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.166+4698G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50500102 | ||||||
| chr14:50500186
|
A | G | 62 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(59): Show | 63 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(60): Show |
intron_variant | MODIFIER | c.166+4614T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50500186 | ||||||
| chr14:50500189
|
G | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(10): Show | 14 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.166+4611C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50500189 | ||||||
| chr14:50500251
|
T | C | 4 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217others(1): Show | 4 | HG02257.hp2 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.166+4549A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50500251 | ||||||
| chr14:50500424
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0036 | 2 | HG02257.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.166+4376C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50500424 | ||||||
| chr14:50500441
|
T | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(59): Show | 63 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(60): Show |
intron_variant | MODIFIER | c.166+4359A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50500441 | ||||||
| chr14:50500511
|
T | C | 15 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(12): Show | 15 | HG00408.hp2 HG00423.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.166+4289A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50500511 | ||||||
| chr14:50500636
|
C | T | 4 | a0001c0006t0001g0231a0001c0006t0001g0232a0001c0006t0001g0233others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.166+4164G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50500636 | ||||||
| chr14:50500901
|
T | C | 1 | a0002c0002t0001g0076 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.166+3899A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50500901 | ||||||
| chr14:50500914
|
T | C | 1 | a0007c0016t0011g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.166+3886A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50500914 | ||||||
| chr14:50500942
|
T | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(60): Show | 64 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(61): Show |
intron_variant | MODIFIER | c.166+3858A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50500942 | ||||||
| chr14:50500969
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.166+3831A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50500969 | ||||||
| chr14:50501043
|
T | G | 1 | a0001c0001t0001g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.166+3757A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50501043 | ||||||
| chr14:50501214
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.166+3586C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50501214 | ||||||
| chr14:50501230
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.166+3570A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50501230 | ||||||
| chr14:50501638
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.166+3162A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50501638 | ||||||
| chr14:50501642
|
G | A | 1 | a0001c0001t0003g0159 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.166+3158C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50501642 | ||||||
| chr14:50501656
|
T | C | 49 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0047others(46): Show | 49 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.166+3144A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50501656 | ||||||
| chr14:50501917
|
T | C | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG00733.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.166+2883A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50501917 | ||||||
| chr14:50502094
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.166+2706A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50502094 | ||||||
| chr14:50502239
|
G | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(20): Show | 24 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.166+2561C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50502239 | ||||||
| chr14:50502327
|
C | T | 4 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217others(1): Show | 4 | HG02257.hp2 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.166+2473G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50502327 | ||||||
| chr14:50502492
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.166+2308A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50502492 | ||||||
| chr14:50502615
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.166+2185C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50502615 | ||||||
| chr14:50502682
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(28): Show | 32 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.166+2118C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50502682 | ||||||
| chr14:50502691
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.166+2109C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50502691 | ||||||
| chr14:50502730
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.166+2070A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50502730 | ||||||
| chr14:50502877
|
T | C | 2 | a0005c0010t0001g0063a0005c0010t0001g0064 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.166+1923A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50502877 | ||||||
| chr14:50503089
|
GA | G | 21 | a0001c0001t0001g0140a0001c0001t0001g0192a0001c0001t0001g0194others(18): Show | 21 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(18): Show |
intron_variant | MODIFIER | c.166+1710delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50503089 | ||||||
| chr14:50503325
|
T | G | 1 | a0001c0001t0001g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.166+1475A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50503325 | ||||||
| chr14:50503337
|
G | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(219): Show | 228 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.166+1463C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50503337 | ||||||
| chr14:50503348
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.166+1452A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50503348 | ||||||
| chr14:50503464
|
C | T | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG00733.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.166+1336G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50503464 | ||||||
| chr14:50503629
|
T | C | 1 | a0001c0004t0001g0111 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.166+1171A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50503629 | ||||||
| chr14:50503739
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.166+1061G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50503739 | ||||||
| chr14:50503874
|
C | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(22): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.166+926G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50503874 | ||||||
| chr14:50503895
|
C | A | 2 | a0001c0001t0003g0131a0001c0001t0012g0179 | 2 | NA18955.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.166+905G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50503895 | ||||||
| chr14:50504002
|
C | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 211 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.166+798G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50504002 | ||||||
| chr14:50504340
|
A | C | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.166+460T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50504340 | ||||||
| chr14:50504368
|
C | A | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.166+432G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50504368 | ||||||
| chr14:50504467
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.166+333T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50504467 | ||||||
| chr14:50504728
|
C | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 234 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.166+72G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 3/32 | chr14 | 50504728 | ||||||
| chr14:50505027
|
T | C | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.109-170A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50505027 | ||||||
| chr14:50505268
|
T | C | 4 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217others(1): Show | 4 | HG02257.hp2 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-411A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50505268 | ||||||
| chr14:50505602
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.109-745A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50505602 | ||||||
| chr14:50505762
|
G | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(1): Show | 4 | HG02523.hp2 NA18944.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-905C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50505762 | ||||||
| chr14:50505834
|
C | T | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.109-977G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50505834 | ||||||
| chr14:50505923
|
TG | T | 45 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0115others(42): Show | 46 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.109-1067delC | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50505923 | ||||||
| chr14:50506039
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.109-1182T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50506039 | ||||||
| chr14:50506187
|
G | C | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.109-1330C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50506187 | ||||||
| chr14:50506299
|
G | T | 1 | a0001c0001t0001g0140 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.109-1442C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50506299 | ||||||
| chr14:50506308
|
T | A | 1 | a0001c0001t0001g0113 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.109-1451A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50506308 | ||||||
| chr14:50506349
|
TTTTG | T | 6 | a0001c0001t0001g0180a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-1496_109-1493d others(6): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50506349 | ||||||
| chr14:50506547
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0026 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.109-1690G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50506547 | ||||||
| chr14:50506548
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(28): Show | 32 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.109-1691C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50506548 | ||||||
| chr14:50506611
|
G | C | 7 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(4): Show | 8 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-1754C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50506611 | ||||||
| chr14:50506648
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0056 | 4 | HG01884.hp2 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-1791G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50506648 | ||||||
| chr14:50506817
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.109-1960G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50506817 | ||||||
| chr14:50506872
|
C | G | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.109-2015G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50506872 | ||||||
| chr14:50506914
|
C | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(4): Show | 7 | HG00733.hp1 HG00735.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.109-2057G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50506914 | ||||||
| chr14:50506919
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0003g0172 | 3 | NA18950.hp2 NA18988.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.109-2062C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50506919 | ||||||
| chr14:50507054
|
T | C | 4 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(1): Show | 5 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-2197A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50507054 | ||||||
| chr14:50507297
|
A | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(28): Show | 32 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.109-2440T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50507297 | ||||||
| chr14:50507306
|
C | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0056 | 4 | HG01884.hp2 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-2449G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50507306 | ||||||
| chr14:50507405
|
G | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 223 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.109-2548C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50507405 | ||||||
| chr14:50507696
|
C | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(28): Show | 32 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.109-2839G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50507696 | ||||||
| chr14:50507769
|
T | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(2): Show | 5 | HG01261.hp2 HG01496.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.109-2912A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50507769 | ||||||
| chr14:50507852
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.109-2995A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50507852 | ||||||
| chr14:50507982
|
G | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.109-3125C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50507982 | ||||||
| chr14:50508380
|
T | G | 8 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(5): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.109-3523A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50508380 | ||||||
| chr14:50508433
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(28): Show | 32 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.109-3576C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50508433 | ||||||
| chr14:50508572
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.109-3715C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50508572 | ||||||
| chr14:50508712
|
TA | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(22): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.109-3856delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50508712 | ||||||
| chr14:50508726
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.109-3869G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50508726 | ||||||
| chr14:50508758
|
T | C | 1 | a0001c0001t0003g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.109-3901A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50508758 | ||||||
| chr14:50508856
|
T | C | 1 | a0001c0001t0002g0018 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.109-3999A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50508856 | ||||||
| chr14:50508957
|
A | G | 2 | a0001c0004t0001g0081a0002c0002t0007g0037 | 2 | HG01071.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.109-4100T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50508957 | ||||||
| chr14:50509293
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.109-4436T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509293 | ||||||
| chr14:50509420
|
C | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 222 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.109-4563G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509420 | ||||||
| chr14:50509427
|
A | G | 4 | a0001c0006t0001g0231a0001c0006t0001g0232a0001c0006t0001g0233others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-4570T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509427 | ||||||
| chr14:50509511
|
A | G | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.109-4654T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509511 | ||||||
| chr14:50509515
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | NA18944.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.109-4658C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509515 | ||||||
| chr14:50509576
|
A | G | 5 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217others(2): Show | 5 | HG02257.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-4719T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509576 | ||||||
| chr14:50509603
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 239 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.109-4746A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509603 | ||||||
| chr14:50509617
|
C | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 222 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.109-4760G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509617 | ||||||
| chr14:50509665
|
A | T | 4 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(1): Show | 5 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-4808T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509665 | ||||||
| chr14:50509673
|
T | TA | 10 | a0001c0001t0001g0117a0001c0001t0001g0126a0001c0001t0001g0127others(7): Show | 10 | HG01928.hp2 HG02071.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.109-4817dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509673 | ||||||
| chr14:50509673
|
TA | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(30): Show | 34 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.109-4817delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509673 | ||||||
| chr14:50509689
|
G | C | 2 | a0001c0001t0001g0075a0002c0002t0001g0051 | 2 | HG01258.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.109-4832C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509689 | ||||||
| chr14:50509706
|
T | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 16 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.109-4849A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509706 | ||||||
| chr14:50509799
|
T | G | 1 | a0001c0001t0001g0035 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.109-4942A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509799 | ||||||
| chr14:50509826
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.109-4969A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509826 | ||||||
| chr14:50509956
|
T | A | 38 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0001g0083others(35): Show | 38 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.109-5099A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509956 | ||||||
| chr14:50509969
|
C | T | 1 | a0007c0016t0011g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.109-5112G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50509969 | ||||||
| chr14:50510005
|
G | C | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.109-5148C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50510005 | ||||||
| chr14:50510180
|
C | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(158): Show | 164 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.109-5323G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50510180 | ||||||
| chr14:50510316
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01261.hp2 HG01496.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.109-5459G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50510316 | ||||||
| chr14:50510368
|
G | C | 1 | a0007c0016t0011g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.109-5511C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50510368 | ||||||
| chr14:50510486
|
T | C | 1 | a0001c0001t0012g0179 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.109-5629A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50510486 | ||||||
| chr14:50510702
|
C | T | 4 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0116others(1): Show | 4 | HG02027.hp1 NA19056.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-5845G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50510702 | ||||||
| chr14:50510708
|
T | A | 5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(2): Show | 5 | HG01261.hp2 HG01496.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.109-5851A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50510708 | ||||||
| chr14:50510762
|
C | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.109-5905G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50510762 | ||||||
| chr14:50510765
|
T | A | 1 | a0001c0001t0001g0112 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.109-5908A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50510765 | ||||||
| chr14:50510765
|
T | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(157): Show | 163 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.109-5908A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50510765 | ||||||
| chr14:50510894
|
T | A | 16 | a0001c0001t0001g0140a0001c0001t0001g0194a0001c0001t0001g0195others(13): Show | 16 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(13): Show |
intron_variant | MODIFIER | c.109-6037A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50510894 | ||||||
| chr14:50511117
|
T | C | 1 | a0001c0017t0001g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.109-6260A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50511117 | ||||||
| chr14:50511434
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01069.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.109-6577T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50511434 | ||||||
| chr14:50511527
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.109-6670A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50511527 | ||||||
| chr14:50511746
|
C | T | 1 | a0001c0014t0001g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.109-6889G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50511746 | ||||||
| chr14:50511763
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.109-6906G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50511763 | ||||||
| chr14:50511833
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.109-6976G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50511833 | ||||||
| chr14:50512027
|
T | A | 1 | a0001c0001t0001g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.109-7170A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50512027 | ||||||
| chr14:50512157
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.109-7300A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50512157 | ||||||
| chr14:50512405
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.109-7548T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50512405 | ||||||
| chr14:50512489
|
A | C | 1 | a0001c0001t0002g0020 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.109-7632T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50512489 | ||||||
| chr14:50512651
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 222 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.109-7794C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50512651 | ||||||
| chr14:50512777
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.109-7920G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50512777 | ||||||
| chr14:50512939
|
C | T | 1 | a0007c0016t0011g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.109-8082G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50512939 | ||||||
| chr14:50512958
|
A | C | 1 | a0001c0001t0002g0019 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.109-8101T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50512958 | ||||||
| chr14:50512985
|
A | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0056a0001c0001t0001g0077 | 5 | HG01884.hp2 HG02559.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.109-8128T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50512985 | ||||||
| chr14:50513084
|
C | G | 5 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217others(2): Show | 5 | HG02257.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-8227G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50513084 | ||||||
| chr14:50513086
|
T | C | 7 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0183others(4): Show | 7 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.109-8229A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50513086 | ||||||
| chr14:50513587
|
TAA | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.109-8732_109-8731d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50513587 | ||||||
| chr14:50513716
|
C | G | 1 | a0001c0001t0001g0120 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.109-8859G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50513716 | ||||||
| chr14:50513718
|
G | C | 1 | a0001c0003t0001g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.109-8861C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50513718 | ||||||
| chr14:50513823
|
A | C | 1 | a0001c0001t0001g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.109-8966T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50513823 | ||||||
| chr14:50513885
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.109-9028T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50513885 | ||||||
| chr14:50514129
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(21): Show | 25 | HG00733.hp2 HG01256.hp2 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.109-9272C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50514129 | ||||||
| chr14:50514166
|
C | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(158): Show | 164 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.109-9309G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50514166 | ||||||
| chr14:50514243
|
A | AT | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(158): Show | 164 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.109-9387dupA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50514243 | ||||||
| chr14:50514451
|
G | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.109-9594C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50514451 | ||||||
| chr14:50514499
|
G | A | 8 | a0001c0001t0001g0075a0001c0004t0001g0081a0002c0002t0001g0051others(5): Show | 8 | HG00741.hp2 HG01071.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.109-9642C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50514499 | ||||||
| chr14:50514535
|
G | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.109-9678C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50514535 | ||||||
| chr14:50514778
|
G | C | 1 | a0001c0001t0001g0165 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.109-9921C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50514778 | ||||||
| chr14:50514848
|
AT | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(156): Show | 162 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.109-9992delA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50514848 | ||||||
| chr14:50514904
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.109-10047T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50514904 | ||||||
| chr14:50514907
|
CT | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.109-10051delA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50514907 | ||||||
| chr14:50514928
|
G | T | 1 | a0001c0007t0001g0215 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.109-10071C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50514928 | ||||||
| chr14:50514942
|
C | T | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.109-10085G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50514942 | ||||||
| chr14:50514943
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0006t0001g0232others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-10086C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50514943 | ||||||
| chr14:50515028
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01069.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.109-10171G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50515028 | ||||||
| chr14:50515029
|
G | A | 7 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0183others(4): Show | 7 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.109-10172C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50515029 | ||||||
| chr14:50515061
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.109-10204C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50515061 | ||||||
| chr14:50515109
|
G | A | 7 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.109-10252C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50515109 | ||||||
| chr14:50515419
|
C | A | 2 | a0001c0006t0001g0232a0001c0006t0001g0233 | 2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.109-10562G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50515419 | ||||||
| chr14:50515451
|
C | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(29): Show | 33 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.109-10594G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50515451 | ||||||
| chr14:50515602
|
T | C | 1 | a0003c0009t0001g0176 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.109-10745A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50515602 | ||||||
| chr14:50515832
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.109-10975T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50515832 | ||||||
| chr14:50516265
|
C | T | 16 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(13): Show | 16 | HG00140.hp2 HG00738.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.109-11408G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50516265 | ||||||
| chr14:50516471
|
G | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0115others(41): Show | 45 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.109-11614C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50516471 | ||||||
| chr14:50516532
|
A | G | 6 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-11675T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50516532 | ||||||
| chr14:50516545
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01261.hp2 HG01496.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.109-11688G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50516545 | ||||||
| chr14:50516931
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0116 | 2 | HG02027.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.109-12074G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50516931 | ||||||
| chr14:50517340
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.109-12483G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50517340 | ||||||
| chr14:50517659
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.109-12802G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50517659 | ||||||
| chr14:50517798
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 228 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.109-12941G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50517798 | ||||||
| chr14:50518318
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.109-13461T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50518318 | ||||||
| chr14:50518489
|
C | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0180others(29): Show | 33 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.108+13453G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50518489 | ||||||
| chr14:50518719
|
T | A | 1 | a0001c0001t0001g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.108+13223A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50518719 | ||||||
| chr14:50518892
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.108+13050A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50518892 | ||||||
| chr14:50518963
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.108+12979T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50518963 | ||||||
| chr14:50519004
|
G | C | 1 | a0001c0001t0001g0204 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.108+12938C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50519004 | ||||||
| chr14:50519169
|
AGTT | A | 15 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 16 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.108+12770_108+1277 others(7): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50519169 | ||||||
| chr14:50519314
|
T | C | 1 | a0001c0001t0001g0003 | 2 | HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.108+12628A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50519314 | ||||||
| chr14:50519413
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(111): Show | 117 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(114): Show |
intron_variant | MODIFIER | c.108+12529C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50519413 | ||||||
| chr14:50519515
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.108+12427C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50519515 | ||||||
| chr14:50519540
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.108+12402C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50519540 | ||||||
| chr14:50519632
|
C | T | 2 | a0001c0006t0001g0231a0001c0006t0010g0234 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.108+12310G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50519632 | ||||||
| chr14:50519633
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.108+12309C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50519633 | ||||||
| chr14:50519950
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0210 | 3 | HG01069.hp1 HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.108+11992T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50519950 | ||||||
| chr14:50520146
|
C | T | 2 | a0005c0010t0001g0063a0005c0010t0001g0064 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.108+11796G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50520146 | ||||||
| chr14:50520236
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0192others(22): Show | 26 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.108+11706G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50520236 | ||||||
| chr14:50520426
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.108+11516C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50520426 | ||||||
| chr14:50520465
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.108+11477G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50520465 | ||||||
| chr14:50520479
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.108+11463G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50520479 | ||||||
| chr14:50520495
|
T | C | 1 | a0001c0001t0001g0003 | 2 | HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.108+11447A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50520495 | ||||||
| chr14:50520551
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 9 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.108+11391A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50520551 | ||||||
| chr14:50520629
|
A | G | 2 | a0001c0007t0001g0215a0001c0007t0001g0217 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.108+11313T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50520629 | ||||||
| chr14:50520763
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(111): Show | 117 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(114): Show |
intron_variant | MODIFIER | c.108+11179G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50520763 | ||||||
| chr14:50520820
|
CT | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(115): Show | 121 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(118): Show |
intron_variant | MODIFIER | c.108+11121delA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50520820 | ||||||
| chr14:50520880
|
T | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 9 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.108+11062A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50520880 | ||||||
| chr14:50520895
|
C | T | 2 | a0001c0006t0001g0231a0001c0006t0010g0234 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.108+11047G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50520895 | ||||||
| chr14:50521003
|
C | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.108+10939G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50521003 | ||||||
| chr14:50521117
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.108+10825C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50521117 | ||||||
| chr14:50521255
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.108+10687C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50521255 | ||||||
| chr14:50521271
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.108+10671A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50521271 | ||||||
| chr14:50521336
|
T | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(2): Show | 5 | HG01261.hp2 HG01496.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.108+10606A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50521336 | ||||||
| chr14:50521347
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.108+10595T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50521347 | ||||||
| chr14:50521393
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.108+10549G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50521393 | ||||||
| chr14:50521670
|
G | T | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.108+10272C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50521670 | ||||||
| chr14:50521821
|
G | C | 1 | a0001c0001t0001g0036 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.108+10121C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50521821 | ||||||
| chr14:50522024
|
T | C | 1 | a0001c0003t0001g0220 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.108+9918A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50522024 | ||||||
| chr14:50522072
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.108+9870A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50522072 | ||||||
| chr14:50522200
|
A | G | 49 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0047others(46): Show | 49 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.108+9742T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50522200 | ||||||
| chr14:50522260
|
C | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.108+9682G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50522260 | ||||||
| chr14:50522561
|
G | C | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG01361.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.108+9381C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50522561 | ||||||
| chr14:50522757
|
T | C | 1 | a0002c0002t0001g0076 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.108+9185A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50522757 | ||||||
| chr14:50522834
|
A | G | 1 | a0007c0016t0011g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.108+9108T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50522834 | ||||||
| chr14:50522847
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 214 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.108+9095A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50522847 | ||||||
| chr14:50523119
|
C | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0056a0001c0001t0001g0077 | 5 | HG01884.hp2 HG02559.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.108+8823G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523119 | ||||||
| chr14:50523135
|
C | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 221 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.108+8807G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523135 | ||||||
| chr14:50523225
|
C | G | 36 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(33): Show | 36 | HG00140.hp2 HG00738.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.108+8717G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523225 | ||||||
| chr14:50523225
|
C | T | 3 | a0003c0009t0001g0175a0003c0009t0001g0176a0003c0009t0001g0177 | 3 | NA18945.hp1 NA18951.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.108+8717G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523225 | ||||||
| chr14:50523226
|
G | A | 3 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217 | 3 | HG02257.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.108+8716C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523226 | ||||||
| chr14:50523274
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.108+8668C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523274 | ||||||
| chr14:50523371
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.108+8571A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523371 | ||||||
| chr14:50523406
|
A | G | 1 | a0002c0002t0001g0051 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.108+8536T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523406 | ||||||
| chr14:50523463
|
TAAGA | T | 2 | a0003c0009t0001g0175a0003c0009t0001g0176 | 2 | NA18951.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.108+8475_108+8478d others(6): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523463 | ||||||
| chr14:50523472
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.108+8470C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523472 | ||||||
| chr14:50523571
|
G | A | 7 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0183others(4): Show | 7 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+8371C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523571 | ||||||
| chr14:50523574
|
C | G | 1 | a0001c0001t0001g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.108+8368G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523574 | ||||||
| chr14:50523682
|
C | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0180a0001c0001t0001g0181others(28): Show | 32 | HG00408.hp2 HG00423.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.108+8260G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523682 | ||||||
| chr14:50523778
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 9 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.108+8164T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523778 | ||||||
| chr14:50523780
|
A | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.108+8162T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523780 | ||||||
| chr14:50523936
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.108+8006G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50523936 | ||||||
| chr14:50524082
|
T | C | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.108+7860A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50524082 | ||||||
| chr14:50524132
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0166 | 2 | NA18981.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.108+7810C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50524132 | ||||||
| chr14:50524153
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.108+7789G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50524153 | ||||||
| chr14:50524239
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.108+7703A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50524239 | ||||||
| chr14:50524414
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.108+7528G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50524414 | ||||||
| chr14:50524581
|
G | A | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 224 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.108+7361C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50524581 | ||||||
| chr14:50524609
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0026 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.108+7333G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50524609 | ||||||
| chr14:50524631
|
G | C | 1 | a0001c0001t0001g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.108+7311C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50524631 | ||||||
| chr14:50524632
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.108+7310A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50524632 | ||||||
| chr14:50524663
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.108+7279C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50524663 | ||||||
| chr14:50524694
|
C | G | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.108+7248G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50524694 | ||||||
| chr14:50524797
|
CT | C | 5 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217others(2): Show | 5 | HG02257.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.108+7144delA | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50524797 | ||||||
| chr14:50524867
|
G | A | 3 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080 | 3 | HG01433.hp2 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.108+7075C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50524867 | ||||||
| chr14:50524986
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.108+6956C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50524986 | ||||||
| chr14:50525216
|
C | T | 15 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(12): Show | 15 | HG00408.hp2 HG00423.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.108+6726G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50525216 | ||||||
| chr14:50525237
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.108+6705G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50525237 | ||||||
| chr14:50525314
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.108+6628A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50525314 | ||||||
| chr14:50525347
|
C | A | 3 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220 | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+6595G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50525347 | ||||||
| chr14:50525408
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0026 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.108+6534A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50525408 | ||||||
| chr14:50525549
|
C | G | 1 | a0001c0001t0001g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.108+6393G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50525549 | ||||||
| chr14:50525775
|
C | T | 1 | a0001c0014t0001g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.108+6167G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50525775 | ||||||
| chr14:50525776
|
G | A | 20 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(17): Show | 20 | HG01123.hp2 HG01169.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.108+6166C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50525776 | ||||||
| chr14:50525922
|
C | T | 1 | a0007c0016t0011g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.108+6020G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50525922 | ||||||
| chr14:50525926
|
A | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.108+6016T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50525926 | ||||||
| chr14:50526218
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.108+5724A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50526218 | ||||||
| chr14:50526258
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.108+5684C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50526258 | ||||||
| chr14:50526276
|
A | G | 1 | a0001c0014t0001g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.108+5666T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50526276 | ||||||
| chr14:50526339
|
G | T | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.108+5603C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50526339 | ||||||
| chr14:50526361
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0030others(50): Show | 55 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.108+5581C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50526361 | ||||||
| chr14:50526598
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.108+5344C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50526598 | ||||||
| chr14:50526738
|
A | C | 1 | a0001c0001t0001g0003 | 2 | HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.108+5204T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50526738 | ||||||
| chr14:50526960
|
CA | C | 20 | a0001c0001t0001g0192a0001c0001t0001g0194a0001c0001t0001g0195others(17): Show | 20 | HG00408.hp2 HG00423.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.108+4981delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50526960 | ||||||
| chr14:50526986
|
A | G | 1 | a0001c0001t0002g0008 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.108+4956T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50526986 | ||||||
| chr14:50527024
|
G | C | 1 | a0001c0001t0006g0006 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.108+4918C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50527024 | ||||||
| chr14:50527206
|
G | GCA | 13 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(10): Show | 14 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.108+4734_108+4735d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50527206 | ||||||
| chr14:50527228
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.108+4714T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50527228 | ||||||
| chr14:50527296
|
C | T | 18 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(15): Show | 18 | HG01123.hp2 HG01169.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.108+4646G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50527296 | ||||||
| chr14:50527333
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.108+4609G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50527333 | ||||||
| chr14:50527411
|
CA | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0023others(65): Show | 71 | HG00408.hp2 HG00423.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.108+4530delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50527411 | ||||||
| chr14:50527427
|
T | C | 6 | a0001c0003t0001g0005a0001c0003t0001g0221a0001c0006t0001g0231others(3): Show | 7 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+4515A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50527427 | ||||||
| chr14:50527642
|
A | T | 1 | a0001c0001t0001g0002 | 2 | HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.108+4300T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50527642 | ||||||
| chr14:50527658
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.108+4284G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50527658 | ||||||
| chr14:50527761
|
C | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 238 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.108+4181G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50527761 | ||||||
| chr14:50527816
|
AAAT | A | 4 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217others(1): Show | 4 | HG02257.hp2 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+4123_108+4125d others(5): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50527816 | ||||||
| chr14:50527831
|
TAATAATA | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0135others(41): Show | 45 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.108+4104_108+4110d others(9): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50527831 | ||||||
| chr14:50527845
|
TAAATAA | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(176): Show | 184 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.108+4091_108+4096d others(8): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50527845 | ||||||
| chr14:50527849
|
TAA | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0132others(50): Show | 54 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.108+4091_108+4092d others(4): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50527849 | ||||||
| chr14:50527917
|
C | A | 1 | a0001c0001t0001g0134 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.108+4025G>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50527917 | ||||||
| chr14:50528091
|
C | T | 3 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG01358.hp2 HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.108+3851G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50528091 | ||||||
| chr14:50528402
|
T | TA | 5 | a0001c0001t0001g0116a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG02027.hp1 HG02071.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.108+3539dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50528402 | ||||||
| chr14:50528402
|
TA | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 158 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(155): Show |
intron_variant | MODIFIER | c.108+3539delT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50528402 | ||||||
| chr14:50528402
|
TAAA | T | 7 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(4): Show | 7 | HG02027.hp2 NA18950.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.108+3537_108+3539d others(5): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50528402 | ||||||
| chr14:50528660
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.108+3282G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50528660 | ||||||
| chr14:50528827
|
G | A | 4 | a0001c0006t0001g0231a0001c0006t0001g0232a0001c0006t0001g0233others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.108+3115C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50528827 | ||||||
| chr14:50528840
|
C | G | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG00733.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.108+3102G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50528840 | ||||||
| chr14:50529011
|
A | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0180a0001c0001t0001g0181others(28): Show | 32 | HG00408.hp2 HG00423.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.108+2931T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50529011 | ||||||
| chr14:50529149
|
G | A | 7 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0183others(4): Show | 7 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+2793C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50529149 | ||||||
| chr14:50529220
|
T | TA | 32 | a0001c0001t0001g0004a0001c0001t0001g0180a0001c0001t0001g0181others(29): Show | 33 | HG00408.hp2 HG00423.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.108+2721dupT | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50529220 | ||||||
| chr14:50529651
|
AAAC | A | 36 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(33): Show | 36 | HG00140.hp2 HG00738.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.108+2288_108+2290d others(5): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50529651 | ||||||
| chr14:50529974
|
G | T | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(5): Show | 8 | HG00733.hp1 HG00735.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+1968C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50529974 | ||||||
| chr14:50530013
|
G | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.108+1929C>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50530013 | ||||||
| chr14:50530403
|
T | C | 8 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(5): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.108+1539A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50530403 | ||||||
| chr14:50530468
|
C | T | 8 | a0001c0003t0001g0005a0001c0003t0001g0219a0001c0003t0001g0220others(5): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.108+1474G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50530468 | ||||||
| chr14:50530490
|
T | G | 1 | a0001c0014t0001g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.108+1452A>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50530490 | ||||||
| chr14:50530667
|
A | G | 4 | a0001c0007t0001g0215a0001c0007t0001g0216a0001c0007t0001g0217others(1): Show | 4 | HG02257.hp2 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+1275T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50530667 | ||||||
| chr14:50530697
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.108+1245C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50530697 | ||||||
| chr14:50530715
|
A | G | 19 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(16): Show | 20 | HG02055.hp2 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.108+1227T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50530715 | ||||||
| chr14:50530771
|
C | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 238 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.108+1171G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50530771 | ||||||
| chr14:50530827
|
TGTTTG | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 238 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.108+1110_108+1114d others(7): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50530827 | ||||||
| chr14:50530837
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 197 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.108+1105A>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50530837 | ||||||
| chr14:50530867
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 238 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.108+1075T>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50530867 | ||||||
| chr14:50530982
|
T | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0003g0172 | 3 | NA18950.hp2 NA18988.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.108+960A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50530982 | ||||||
| chr14:50531065
|
G | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0041others(114): Show | 119 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.108+877C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50531065 | ||||||
| chr14:50531481
|
A | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.108+461T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50531481 | ||||||
| chr14:50531487
|
C | G | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.108+455G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50531487 | ||||||
| chr14:50531547
|
A | T | 7 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0183others(4): Show | 7 | HG01361.hp1 HG01433.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+395T>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50531547 | ||||||
| chr14:50531625
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.108+317C>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50531625 | ||||||
| chr14:50531851
|
T | A | 1 | a0001c0001t0002g0022 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.108+91A>T | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50531851 | ||||||
| chr14:50531855
|
C | T | 1 | a0001c0001t0002g0007 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.108+87G>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 2/32 | chr14 | 50531855 | ||||||
| chr14:50532255
|
A | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(159): Show | 165 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.-109-97T>G | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 1/32 | chr14 | 50532255 | ||||||
| chr14:50532292
|
C | CA | 15 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 16 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-109-135_-109-134i others(3): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 1/32 | chr14 | 50532292 | ||||||
| chr14:50532293
|
G | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 16 | HG01261.hp2 HG01496.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-109-135C>A | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 1/32 | chr14 | 50532293 | ||||||
| chr14:50532395
|
C | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 218 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-110+53G>C | MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 1/32 | chr14 | 50532395 |