Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8577 |
|---|---|
| ensemblid | ENSG00000241697.5 |
| hgncid | 11866 |
| symbol | TMEFF1 |
| name | transmembrane protein with EGF like and two follistatin like domains 1 |
| refseq_nuc | NM_003692.5 |
| refseq_prot | NP_003683.2 |
| ensembl_nuc | ENST00000374879.5 |
| ensembl_prot | ENSP00000364013.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 100473149 |
| end | 100577636 |
| strand | + |
| ver | v1.2 |
| region | chr9:100473149-100577636 |
| region5000 | chr9:100468149-100582636 |
| regionname0 | TMEFF1_chr9_100473149_100577636 |
| regionname5000 | TMEFF1_chr9_100468149_100582636 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 380 | 242 | 72 | 44 | 80 | 12 | 32 | 56 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1143 | 210 | 57 | 33 | 80 | 10 | 29 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| c0002 | 0/1 | 1143 | 25 | 8 | 11 | 0 | 2 | 3 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| c0003 | 0/0 | 1143 | 7 | 7 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1433 | 166 | 50 | 40 | 40 | 12 | 22 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| t0002 | 0/0 | 1433 | 47 | 6 | 4 | 29 | 0 | 8 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| t0003 | 0/0 | 1433 | 15 | 15 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| t0004 | 0/0 | 1433 | 7 | 0 | 0 | 7 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| t0005 | 0/0 | 1433 | 3 | 0 | 0 | 2 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| t0006 | 0/0 | 1433 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| t0007 | 0/0 | 1433 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| t0008 | 0/0 | 1433 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| t0009 | 0/0 | 1433 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1143 | 210 | 57 | 33 | 80 | 10 | 29 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| a0001c0002 | 0/1 | 1143 | 25 | 8 | 11 | 0 | 2 | 3 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| a0001c0003 | 0/0 | 1143 | 7 | 7 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2575 | 137 | 38 | 29 | 40 | 10 | 19 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| a0001c0001t0002 | 0/0 | 2575 | 47 | 6 | 4 | 29 | 0 | 8 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| a0001c0001t0003 | 0/0 | 2575 | 12 | 12 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| a0001c0001t0004 | 0/0 | 2575 | 7 | 0 | 0 | 7 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| a0001c0001t0005 | 0/0 | 2575 | 3 | 0 | 0 | 2 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| a0001c0001t0006 | 0/0 | 2575 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| a0001c0001t0007 | 0/0 | 2575 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| a0001c0001t0008 | 0/0 | 2575 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| a0001c0001t0009 | 0/0 | 2575 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| a0001c0002t0001 | 0/1 | 2575 | 22 | 5 | 11 | 0 | 2 | 3 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| a0001c0002t0003 | 0/0 | 2575 | 3 | 3 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| a0001c0003t0001 | 0/0 | 2575 | 7 | 7 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | copy fasta | chr9 | 100468149 | 100582636 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0007g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0008g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0001t0009g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0002t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | FIN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | FIN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | CHS | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | CHS | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0086 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0081 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0127 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | PEL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02056 | hp1 | a0001 | c0001 | t0008 | g0209 | EAS | KHV | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | KHV | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | KHV | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0075 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0151 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0107 | EAS | KHV | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0077 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0152 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0145 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | ESN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0153 | AFR | ESN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0193 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0132 | AFR | MSL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0149 | AFR | ESN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | MSL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03453 | hp2 | a0001 | c0002 | t0003 | g0133 | AFR | MSL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0091 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | ESN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ESN | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0210 | AFR | MSL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | MSL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03688 | hp1 | a0001 | c0001 | t0007 | g0191 | SAS | STU | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | STU | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | BEB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | STU | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | STU | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | STU | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | STU | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | STU | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18522 | hp1 | a0001 | c0002 | t0003 | g0146 | AFR | YRI | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0158 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0023 | AFR | LWK | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | LWK | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | LWK | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0073 | EUR | TSI | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0020 | EUR | TSI | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | GIH | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | GIH | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | CLM | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0074 | AFR | ACB | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0150 | AFR | MSL | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18955 | hp1 | a0001 | c0001 | t0009 | g0031 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | USA | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | USA | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | LWK | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0130 | REF | REF | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0224 | REF | REF | TMEFF1_chr9_100468149_100582636 | TMEFF1 | chr9 | 100468149 | 100582636 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100473571
|
G | T | 1 | a0001c0002 | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
synonymous_variant | LOW | c.27G>T | p.Pro9Pro | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/10 | 423/2575 | 27/1143 | 9/380 | chr9 | 100473571 | ||
| chr9:100561446
|
C | T | 1 | a0001c0003 | 7 | HG01891.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
synonymous_variant | LOW | c.825C>T | p.Cys275Cys | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/10 | 1221/2575 | 825/1143 | 275/380 | chr9 | 100561446 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100473226
|
G | C | 1 | a0001c0001t0006 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-319G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/10 | 319 | chr9 | 100473226 | |||||
| chr9:100473508
|
G | A | 3 | a0001c0001t0002a0001c0001t0005a0001c0001t0007 | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
5_prime_UTR_variant | MODIFIER | c.-37G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/10 | 37 | chr9 | 100473508 | |||||
| chr9:100576724
|
C | T | 1 | a0001c0001t0009 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*124C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 10/10 | 124 | chr9 | 100576724 | |||||
| chr9:100576971
|
G | A | 1 | a0001c0001t0008 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*371G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 10/10 | 371 | chr9 | 100576971 | |||||
| chr9:100577252
|
A | G | 2 | a0001c0001t0003a0001c0002t0003 | 15 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*652A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 10/10 | 652 | chr9 | 100577252 | |||||
| chr9:100577283
|
A | T | 1 | a0001c0001t0007 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*683A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 10/10 | 683 | chr9 | 100577283 | |||||
| chr9:100577558
|
A | G | 3 | a0001c0001t0002a0001c0001t0004a0001c0001t0007 | 55 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*958A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 10/10 | 958 | chr9 | 100577558 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100473832
|
C | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+92C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100473832 | ||||||
| chr9:100473998
|
TGGGGCC | T | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.196+273_196+278del others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100473998 | |||||
| chr9:100474037
|
C | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 210 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.196+297C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100474037 | ||||||
| chr9:100474214
|
T | C | 1 | a0001c0002t0001g0020 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.196+474T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100474214 | ||||||
| chr9:100474229
|
C | T | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196+489C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100474229 | ||||||
| chr9:100474332
|
C | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0242a0001c0001t0008g0209 | 3 | HG02056.hp1 HG02818.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.196+592C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100474332 | ||||||
| chr9:100474338
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.196+598C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100474338 | ||||||
| chr9:100474383
|
T | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG01255.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.196+643T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100474383 | ||||||
| chr9:100474548
|
C | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+808C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100474548 | ||||||
| chr9:100474571
|
G | A | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196+831G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100474571 | ||||||
| chr9:100475114
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.196+1374G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100475114 | ||||||
| chr9:100475300
|
T | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(3): Show | 6 | HG00738.hp2 HG01123.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+1560T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100475300 | ||||||
| chr9:100475339
|
T | G | 45 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(42): Show | 45 | HG00408.hp1 HG00423.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.196+1599T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100475339 | ||||||
| chr9:100475715
|
C | CTG | 17 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0032others(14): Show | 17 | HG00323.hp1 HG01255.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.196+2015_196+2016d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100475715 | |||||
| chr9:100475715
|
C | CTGTG | 6 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0004g0211others(3): Show | 6 | HG01192.hp1 HG01243.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+2013_196+2016d others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100475715 | |||||
| chr9:100475715
|
C | CTGTGTG | 16 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(13): Show | 16 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.196+2011_196+2016d others(8): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100475715 | |||||
| chr9:100475715
|
CTG | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0024others(7): Show | 10 | HG00639.hp2 HG01081.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+2015_196+2016d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100475715 | |||||
| chr9:100475715
|
CTGTG | C | 40 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(37): Show | 40 | HG00735.hp1 HG00738.hp2 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.196+2013_196+2016d others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100475715 | |||||
| chr9:100475715
|
CTGTGTG | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0154a0001c0001t0006g0023 | 3 | HG03209.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.196+2011_196+2016d others(8): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100475715 | |||||
| chr9:100475715
|
CTGTGTGT others(5): Show |
C | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+2005_196+2016d others(14): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100475715 | |||||
| chr9:100475806
|
G | A | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.196+2066G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100475806 | ||||||
| chr9:100475932
|
G | A | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+2192G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100475932 | ||||||
| chr9:100475944
|
A | G | 1 | a0001c0001t0003g0018 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.196+2204A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100475944 | ||||||
| chr9:100476145
|
GAT | G | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+2409_196+2410d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100476145 | |||||
| chr9:100476287
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 148 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.196+2547G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100476287 | ||||||
| chr9:100476420
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.196+2680A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100476420 | ||||||
| chr9:100476486
|
C | G | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.196+2746C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100476486 | ||||||
| chr9:100476546
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.196+2806C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100476546 | ||||||
| chr9:100476656
|
G | C | 5 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | NA18941.hp2 NA18942.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+2916G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100476656 | ||||||
| chr9:100476699
|
G | GT | 25 | a0001c0001t0001g0029a0001c0001t0001g0068a0001c0001t0001g0069others(22): Show | 25 | HG00423.hp2 HG00733.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.196+2974dupT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100476699 | |||||
| chr9:100476699
|
G | GTT | 21 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.196+2973_196+2974d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100476699 | |||||
| chr9:100476721
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.196+2981G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100476721 | ||||||
| chr9:100476782
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.196+3042C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100476782 | ||||||
| chr9:100476795
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+3055C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100476795 | ||||||
| chr9:100476917
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | NA18941.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.196+3177C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100476917 | ||||||
| chr9:100476985
|
C | T | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.196+3245C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100476985 | ||||||
| chr9:100476987
|
C | T | 1 | a0001c0001t0004g0211 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.196+3247C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100476987 | ||||||
| chr9:100477031
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.196+3291C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477031 | ||||||
| chr9:100477038
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.196+3298G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477038 | ||||||
| chr9:100477076
|
C | T | 8 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(5): Show | 8 | HG00735.hp1 HG03017.hp2 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.196+3336C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477076 | ||||||
| chr9:100477147
|
A | G | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196+3407A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477147 | ||||||
| chr9:100477150
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 107 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.196+3410A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477150 | ||||||
| chr9:100477211
|
T | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG00408.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.196+3471T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477211 | ||||||
| chr9:100477326
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.196+3586C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477326 | ||||||
| chr9:100477344
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.196+3604C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477344 | ||||||
| chr9:100477393
|
T | C | 3 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157 | 3 | HG00408.hp2 NA19003.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.196+3653T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477393 | ||||||
| chr9:100477617
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.196+3877C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477617 | ||||||
| chr9:100477620
|
C | CT | 12 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0066others(9): Show | 12 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.196+3903dupT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100477620 | |||||
| chr9:100477620
|
CT | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(78): Show | 81 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.196+3903delT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100477620 | |||||
| chr9:100477638
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.196+3898T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477638 | ||||||
| chr9:100477652
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.196+3912G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477652 | ||||||
| chr9:100477771
|
C | T | 34 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0002t0001g0020others(31): Show | 34 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.196+4031C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477771 | ||||||
| chr9:100477798
|
T | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+4058T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477798 | ||||||
| chr9:100477828
|
T | A | 1 | a0001c0003t0001g0145 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.196+4088T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477828 | ||||||
| chr9:100477918
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+4178C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477918 | ||||||
| chr9:100477922
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0143 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.196+4182C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477922 | ||||||
| chr9:100477963
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.196+4223A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477963 | ||||||
| chr9:100477977
|
G | A | 34 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0002t0001g0020others(31): Show | 34 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.196+4237G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100477977 | ||||||
| chr9:100478120
|
T | C | 2 | a0001c0002t0003g0132a0001c0002t0003g0146 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.196+4380T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100478120 | ||||||
| chr9:100478153
|
G | A | 21 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.196+4413G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100478153 | ||||||
| chr9:100478448
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 107 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.196+4708A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100478448 | ||||||
| chr9:100478707
|
TACATG | T | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+4972_196+4976d others(7): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100478707 | |||||
| chr9:100478713
|
A | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA19002.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.196+4973A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100478713 | ||||||
| chr9:100478777
|
T | C | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.196+5037T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100478777 | ||||||
| chr9:100478786
|
T | A | 1 | a0001c0001t0004g0211 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.196+5046T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100478786 | ||||||
| chr9:100478978
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.196+5238G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100478978 | ||||||
| chr9:100479023
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.196+5283C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100479023 | ||||||
| chr9:100479133
|
T | C | 21 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.196+5393T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100479133 | ||||||
| chr9:100479150
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.196+5410G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100479150 | ||||||
| chr9:100479385
|
C | T | 67 | a0001c0001t0001g0019a0001c0001t0001g0206a0001c0001t0001g0207others(64): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.196+5645C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100479385 | ||||||
| chr9:100479386
|
G | A | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196+5646G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100479386 | ||||||
| chr9:100479452
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 107 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.196+5712G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100479452 | ||||||
| chr9:100479536
|
C | T | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196+5796C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100479536 | ||||||
| chr9:100479648
|
C | T | 9 | a0001c0001t0001g0095a0001c0001t0001g0119a0001c0001t0001g0120others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.196+5908C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100479648 | ||||||
| chr9:100479769
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.196+6029A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100479769 | ||||||
| chr9:100480040
|
T | C | 1 | a0001c0001t0002g0199 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.196+6300T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100480040 | ||||||
| chr9:100480092
|
G | A | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.196+6352G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100480092 | ||||||
| chr9:100480171
|
T | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+6431T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100480171 | ||||||
| chr9:100480184
|
A | G | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 12 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.196+6444A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100480184 | ||||||
| chr9:100480300
|
C | T | 2 | a0001c0001t0002g0197a0001c0001t0002g0198 | 2 | NA18959.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.196+6560C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100480300 | ||||||
| chr9:100480367
|
A | G | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.196+6627A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100480367 | ||||||
| chr9:100480450
|
C | T | 1 | a0001c0001t0002g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.196+6710C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100480450 | ||||||
| chr9:100480766
|
T | G | 5 | a0001c0001t0002g0159a0001c0001t0002g0160a0001c0001t0002g0197others(2): Show | 5 | HG00423.hp1 HG00544.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+7026T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100480766 | ||||||
| chr9:100481007
|
A | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.196+7267A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100481007 | ||||||
| chr9:100481024
|
T | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+7284T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100481024 | ||||||
| chr9:100481213
|
G | GACATAC | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+7474_196+7479d others(8): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100481213 | |||||
| chr9:100481361
|
A | G | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+7621A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100481361 | ||||||
| chr9:100481523
|
G | A | 7 | a0001c0003t0001g0127a0001c0003t0001g0145a0001c0003t0001g0149others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+7783G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100481523 | ||||||
| chr9:100481700
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 107 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.196+7960A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100481700 | ||||||
| chr9:100481791
|
G | A | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+8051G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100481791 | ||||||
| chr9:100481825
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 107 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.196+8085G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100481825 | ||||||
| chr9:100482204
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 107 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.196+8464C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100482204 | ||||||
| chr9:100482256
|
G | A | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.196+8516G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100482256 | ||||||
| chr9:100482307
|
C | T | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0003t0001g0127others(6): Show | 9 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.196+8567C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100482307 | ||||||
| chr9:100482678
|
G | A | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+8938G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100482678 | ||||||
| chr9:100483262
|
C | T | 1 | a0001c0001t0002g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196+9522C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100483262 | ||||||
| chr9:100483372
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+9632C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100483372 | ||||||
| chr9:100483380
|
C | A | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196+9640C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100483380 | ||||||
| chr9:100483500
|
A | AAAAC | 78 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0001g0044others(75): Show | 78 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.196+9787_196+9790d others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100483500 | |||||
| chr9:100483500
|
A | AAAACAAA others(1): Show |
77 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0024others(74): Show | 77 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.196+9783_196+9790d others(10): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100483500 | |||||
| chr9:100483500
|
AAAAC | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(6): Show | 9 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.196+9787_196+9790d others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100483500 | |||||
| chr9:100483500
|
AAAACAAA others(1): Show |
A | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0003t0001g0127others(6): Show | 9 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.196+9783_196+9790d others(10): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100483500 | |||||
| chr9:100483533
|
T | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.196+9793T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100483533 | ||||||
| chr9:100483587
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG00639.hp1 HG01109.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.196+9847G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100483587 | ||||||
| chr9:100483682
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.196+9942A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100483682 | ||||||
| chr9:100483788
|
G | GT | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(55): Show | 58 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.196+10058dupT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100483788 | |||||
| chr9:100483788
|
G | GTT | 50 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.196+10057_196+1005 others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100483788 | |||||
| chr9:100483866
|
A | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.196+10126A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100483866 | ||||||
| chr9:100484146
|
A | T | 2 | a0001c0002t0001g0077a0001c0002t0001g0078 | 2 | HG02602.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.196+10406A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100484146 | ||||||
| chr9:100484150
|
T | TTA | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.196+10413_196+1041 others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100484150 | |||||
| chr9:100484181
|
A | G | 3 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014 | 3 | HG01891.hp2 HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.196+10441A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100484181 | ||||||
| chr9:100484464
|
G | A | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196+10724G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100484464 | ||||||
| chr9:100484506
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.196+10766G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100484506 | ||||||
| chr9:100484507
|
C | T | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.196+10767C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100484507 | ||||||
| chr9:100484608
|
C | A | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+10868C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100484608 | ||||||
| chr9:100484810
|
A | G | 5 | a0001c0001t0001g0093a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG00280.hp2 HG01069.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+11070A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100484810 | ||||||
| chr9:100484832
|
T | C | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.196+11092T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100484832 | ||||||
| chr9:100484959
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+11219G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100484959 | ||||||
| chr9:100485047
|
A | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.196+11307A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100485047 | ||||||
| chr9:100485259
|
G | A | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.196+11519G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100485259 | ||||||
| chr9:100485299
|
A | C | 34 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0002t0001g0020others(31): Show | 34 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.196+11559A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100485299 | ||||||
| chr9:100485365
|
T | A | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.196+11625T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100485365 | ||||||
| chr9:100485656
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.196+11916C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100485656 | ||||||
| chr9:100485697
|
TCTTAA | T | 26 | a0001c0001t0001g0099a0001c0002t0001g0020a0001c0002t0001g0073others(23): Show | 26 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.196+11965_196+1196 others(9): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100485697 | |||||
| chr9:100485886
|
T | G | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.196+12146T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100485886 | ||||||
| chr9:100485911
|
C | T | 1 | a0001c0003t0001g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.196+12171C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100485911 | ||||||
| chr9:100485919
|
C | T | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.196+12179C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100485919 | ||||||
| chr9:100485940
|
A | G | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+12200A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100485940 | ||||||
| chr9:100486039
|
C | CT | 18 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(15): Show | 18 | HG00733.hp2 HG01081.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.196+12312dupT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100486039 | |||||
| chr9:100486357
|
T | C | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.197-12408T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100486357 | ||||||
| chr9:100486381
|
T | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0038 | 2 | NA19004.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.197-12384T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100486381 | ||||||
| chr9:100486391
|
T | C | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.197-12374T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100486391 | ||||||
| chr9:100486504
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.197-12261C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100486504 | ||||||
| chr9:100486776
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 107 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.197-11989A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100486776 | ||||||
| chr9:100486800
|
T | G | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.197-11965T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100486800 | ||||||
| chr9:100486885
|
G | A | 21 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.197-11880G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100486885 | ||||||
| chr9:100487131
|
CTTTAT | C | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.197-11625_197-1162 others(9): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100487131 | |||||
| chr9:100487259
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.197-11506G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100487259 | ||||||
| chr9:100487354
|
G | A | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0003t0001g0127others(6): Show | 9 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.197-11411G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100487354 | ||||||
| chr9:100487460
|
G | A | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.197-11305G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100487460 | ||||||
| chr9:100487575
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.197-11190T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100487575 | ||||||
| chr9:100487612
|
A | G | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.197-11153A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100487612 | ||||||
| chr9:100487769
|
CT | C | 50 | a0001c0001t0002g0155a0001c0001t0002g0157a0001c0001t0002g0159others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.197-10983delT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100487769 | |||||
| chr9:100487769
|
CTT | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(53): Show | 56 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.197-10984_197-1098 others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100487769 | |||||
| chr9:100487867
|
C | G | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0094others(6): Show | 9 | HG01255.hp1 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.197-10898C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100487867 | ||||||
| chr9:100488174
|
C | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 107 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.197-10591C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100488174 | ||||||
| chr9:100488174
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0072 | 2 | HG01928.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.197-10591C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100488174 | ||||||
| chr9:100488239
|
C | T | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.197-10526C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100488239 | ||||||
| chr9:100488465
|
T | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(19): Show | 22 | HG01081.hp1 HG01243.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-10300T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100488465 | ||||||
| chr9:100488949
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.197-9816G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100488949 | ||||||
| chr9:100488969
|
C | T | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.197-9796C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100488969 | ||||||
| chr9:100488978
|
A | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.197-9787A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100488978 | ||||||
| chr9:100489370
|
T | G | 24 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(21): Show | 24 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.197-9395T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100489370 | ||||||
| chr9:100489377
|
A | T | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.197-9388A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100489377 | ||||||
| chr9:100489435
|
C | T | 1 | a0001c0002t0001g0086 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.197-9330C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100489435 | ||||||
| chr9:100489470
|
C | T | 6 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0051others(3): Show | 6 | HG00733.hp1 HG01167.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-9295C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100489470 | ||||||
| chr9:100489546
|
T | C | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.197-9219T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100489546 | ||||||
| chr9:100490113
|
A | C | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.197-8652A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100490113 | ||||||
| chr9:100490530
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(70): Show | 73 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.197-8235T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100490530 | ||||||
| chr9:100490699
|
G | A | 7 | a0001c0003t0001g0127a0001c0003t0001g0145a0001c0003t0001g0149others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-8066G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100490699 | ||||||
| chr9:100490700
|
GT | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(171): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.197-8052delT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100490700 | |||||
| chr9:100490836
|
G | GGT | 106 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0026others(103): Show | 106 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.197-7894_197-7893d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100490836 | |||||
| chr9:100490836
|
G | GGTGT | 35 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(32): Show | 35 | HG00323.hp1 HG00438.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.197-7896_197-7893d others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100490836 | |||||
| chr9:100490836
|
GGTGT | G | 25 | a0001c0001t0001g0028a0001c0002t0001g0020a0001c0002t0001g0073others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.197-7896_197-7893d others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100490836 | |||||
| chr9:100490865
|
G | A | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.197-7900G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100490865 | ||||||
| chr9:100490865
|
G | GTGTGTGT others(1): Show |
39 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163others(36): Show | 39 | HG00438.hp1 HG01070.hp2 HG01952.hp1 others(36): Show |
intron_variant | MODIFIER | c.197-7876_197-7869d others(10): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100490865 | |||||
| chr9:100490865
|
G | GTGTGTGT others(3): Show |
6 | a0001c0001t0002g0159a0001c0001t0002g0197a0001c0001t0002g0198others(3): Show | 6 | HG00423.hp1 HG03017.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-7893_197-7892i others(12): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100490865 | |||||
| chr9:100490865
|
G | GTGTGTGT others(5): Show |
5 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0160others(2): Show | 5 | HG00408.hp2 HG00544.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-7893_197-7892i others(14): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100490865 | |||||
| chr9:100490865
|
G | GTGTGTGT others(7): Show |
3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0002g0155 | 3 | HG02602.hp1 HG03834.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.197-7893_197-7892i others(16): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100490865 | |||||
| chr9:100490924
|
C | T | 1 | a0001c0002t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.197-7841C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100490924 | ||||||
| chr9:100490925
|
C | G | 1 | a0001c0002t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.197-7840C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100490925 | ||||||
| chr9:100490931
|
A | G | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0003t0001g0127others(6): Show | 9 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.197-7834A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100490931 | ||||||
| chr9:100491658
|
A | G | 1 | a0001c0001t0002g0192 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.197-7107A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100491658 | ||||||
| chr9:100491748
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.197-7017T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100491748 | ||||||
| chr9:100491770
|
G | A | 2 | a0001c0002t0001g0089a0001c0002t0001g0091 | 2 | HG01243.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.197-6995G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100491770 | ||||||
| chr9:100491785
|
A | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0154 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.197-6980A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100491785 | ||||||
| chr9:100491853
|
A | G | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.197-6912A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100491853 | ||||||
| chr9:100491882
|
C | CT | 59 | a0001c0001t0001g0022a0001c0001t0001g0094a0001c0001t0001g0099others(56): Show | 59 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.197-6867dupT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100491882 | |||||
| chr9:100491990
|
A | G | 5 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0230others(2): Show | 5 | HG02145.hp1 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-6775A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100491990 | ||||||
| chr9:100492074
|
C | G | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.197-6691C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100492074 | ||||||
| chr9:100492074
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-6691C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100492074 | ||||||
| chr9:100492087
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.197-6678C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100492087 | ||||||
| chr9:100492167
|
A | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG00639.hp1 HG01109.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.197-6598A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100492167 | ||||||
| chr9:100492540
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.197-6225G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100492540 | ||||||
| chr9:100492768
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.197-5997A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100492768 | ||||||
| chr9:100492778
|
C | T | 1 | a0001c0001t0002g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.197-5987C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100492778 | ||||||
| chr9:100492779
|
TGGATCTG others(2988): Show |
T | 1 | a0001c0001t0002g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.197-5985_197-2991d others(2): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100492779 | ||||||
| chr9:100492823
|
G | A | 50 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.197-5942G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100492823 | ||||||
| chr9:100492834
|
G | T | 1 | a0001c0001t0007g0191 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.197-5931G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100492834 | ||||||
| chr9:100492969
|
G | T | 1 | a0001c0002t0001g0131 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.197-5796G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100492969 | ||||||
| chr9:100493184
|
A | G | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.197-5581A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100493184 | ||||||
| chr9:100493232
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.197-5533G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100493232 | ||||||
| chr9:100493321
|
T | C | 4 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 4 | NA18940.hp2 NA18982.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-5444T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100493321 | ||||||
| chr9:100493756
|
C | T | 2 | a0001c0002t0003g0132a0001c0002t0003g0146 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.197-5009C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100493756 | ||||||
| chr9:100493800
|
C | T | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.197-4965C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100493800 | ||||||
| chr9:100494206
|
C | CA | 9 | a0001c0001t0001g0050a0001c0001t0001g0137a0001c0001t0001g0147others(6): Show | 9 | HG00738.hp1 HG02056.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.197-4535dupA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100494206 | |||||
| chr9:100494206
|
CA | C | 60 | a0001c0001t0001g0065a0001c0001t0001g0108a0001c0001t0001g0126others(57): Show | 60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.197-4535delA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100494206 | |||||
| chr9:100494206
|
CAA | C | 6 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(3): Show | 6 | HG02451.hp2 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-4536_197-4535d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100494206 | |||||
| chr9:100494301
|
C | T | 3 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157 | 3 | HG00408.hp2 NA19003.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.197-4464C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100494301 | ||||||
| chr9:100494389
|
A | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 93 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.197-4376A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100494389 | ||||||
| chr9:100494880
|
A | G | 50 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.197-3885A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100494880 | ||||||
| chr9:100495061
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.197-3704G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100495061 | ||||||
| chr9:100495178
|
A | G | 50 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.197-3587A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100495178 | ||||||
| chr9:100495345
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.197-3420A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100495345 | ||||||
| chr9:100495487
|
C | A | 1 | a0001c0001t0002g0164 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.197-3278C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100495487 | ||||||
| chr9:100495651
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.197-3114G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100495651 | ||||||
| chr9:100495762
|
A | C | 1 | a0001c0001t0002g0186 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.197-3003A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100495762 | ||||||
| chr9:100495776
|
C | A | 1 | a0001c0001t0002g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.197-2989C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100495776 | ||||||
| chr9:100495779
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.197-2986G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100495779 | ||||||
| chr9:100495780
|
C | A | 1 | a0001c0001t0002g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.197-2985C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100495780 | ||||||
| chr9:100495781
|
A | T | 1 | a0001c0001t0002g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.197-2984A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100495781 | ||||||
| chr9:100495782
|
C | G | 1 | a0001c0001t0002g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.197-2983C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100495782 | ||||||
| chr9:100495873
|
A | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-2892A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100495873 | ||||||
| chr9:100495919
|
G | A | 3 | a0001c0001t0004g0101a0001c0001t0004g0102a0001c0001t0004g0103 | 3 | NA18942.hp2 NA19000.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.197-2846G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100495919 | ||||||
| chr9:100495950
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(91): Show | 94 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.197-2815G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100495950 | ||||||
| chr9:100496054
|
G | A | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.197-2711G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100496054 | ||||||
| chr9:100496057
|
T | G | 1 | a0001c0001t0001g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.197-2708T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100496057 | ||||||
| chr9:100496089
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 109 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.197-2676A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100496089 | ||||||
| chr9:100496527
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.197-2238A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100496527 | ||||||
| chr9:100496952
|
T | C | 1 | a0001c0001t0003g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.197-1813T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100496952 | ||||||
| chr9:100497006
|
T | C | 1 | a0001c0001t0003g0007 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.197-1759T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100497006 | ||||||
| chr9:100497064
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.197-1701C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100497064 | ||||||
| chr9:100497187
|
G | T | 1 | a0001c0001t0003g0011 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.197-1578G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100497187 | ||||||
| chr9:100497231
|
G | A | 5 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0230others(2): Show | 5 | HG02145.hp1 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-1534G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100497231 | ||||||
| chr9:100497320
|
C | CT | 7 | a0001c0001t0001g0006a0001c0001t0001g0057a0001c0001t0001g0099others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-1421dupT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0129a0001c0002t0003g0133 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.197-1430_197-1421d others(12): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(5): Show |
5 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0077others(2): Show | 5 | HG01081.hp2 HG02257.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-1432_197-1421d others(14): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(6): Show |
16 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0002g0168others(13): Show | 16 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.197-1433_197-1421d others(15): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(7): Show |
8 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0078others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-1434_197-1421d others(16): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(8): Show |
3 | a0001c0001t0002g0164a0001c0002t0001g0090a0001c0003t0001g0152 | 3 | HG01192.hp1 HG02622.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.197-1435_197-1421d others(17): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0002g0169 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.197-1437_197-1421d others(19): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(11): Show |
11 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0170others(8): Show | 11 | NA18948.hp1 NA18951.hp2 NA18966.hp1 others(8): Show |
intron_variant | MODIFIER | c.197-1438_197-1421d others(20): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(12): Show |
3 | a0001c0001t0002g0163a0001c0001t0002g0174a0001c0001t0002g0204 | 3 | HG02080.hp1 NA18940.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.197-1439_197-1421d others(21): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(13): Show |
2 | a0001c0001t0002g0175a0001c0001t0002g0196 | 2 | HG04115.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.197-1440_197-1421d others(22): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(16): Show |
4 | a0001c0001t0002g0176a0001c0001t0002g0194a0001c0001t0002g0203others(1): Show | 4 | HG02056.hp2 HG02135.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-1443_197-1421d others(25): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0002g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.197-1444_197-1421d others(26): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0002g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.197-1421_197-1420i others(27): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(20): Show |
2 | a0001c0001t0002g0190a0001c0001t0002g0195 | 2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.197-1421_197-1420i others(29): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(24): Show |
4 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0179others(1): Show | 4 | HG01952.hp1 HG02922.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-1421_197-1420i others(33): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(25): Show |
4 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0197others(1): Show | 4 | HG01070.hp2 HG01975.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-1421_197-1420i others(34): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0002g0186 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.197-1421_197-1420i others(36): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(28): Show |
1 | a0001c0001t0002g0182 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.197-1421_197-1420i others(37): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(30): Show |
2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.197-1421_197-1420i others(39): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(31): Show |
2 | a0001c0001t0002g0160a0001c0001t0005g0158 | 2 | HG00544.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.197-1421_197-1420i others(40): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(35): Show |
1 | a0001c0001t0002g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.197-1421_197-1420i others(44): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(39): Show |
1 | a0001c0001t0002g0159 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.197-1421_197-1420i others(48): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
C | CTTTTTTT others(40): Show |
1 | a0001c0001t0002g0185 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.197-1421_197-1420i others(49): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497320
|
CT | C | 7 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0115others(4): Show | 7 | HG01069.hp2 HG02145.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-1421delT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100497320 | |||||
| chr9:100497508
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 95 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.197-1257G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100497508 | ||||||
| chr9:100497840
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.197-925G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100497840 | ||||||
| chr9:100497910
|
G | T | 52 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.197-855G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100497910 | ||||||
| chr9:100498200
|
G | A | 3 | a0001c0001t0004g0101a0001c0001t0004g0102a0001c0001t0004g0103 | 3 | NA18942.hp2 NA19000.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.197-565G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100498200 | ||||||
| chr9:100498314
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.197-451A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100498314 | ||||||
| chr9:100498406
|
C | G | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.197-359C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100498406 | ||||||
| chr9:100498496
|
A | T | 1 | a0001c0002t0001g0076 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.197-269A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | chr9 | 100498496 | ||||||
| chr9:100498676
|
CT | C | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.197-84delT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100498676 | |||||
| chr9:100498684
|
T | TAC | 19 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(16): Show | 19 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.197-68_197-67dupAC | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 100498684 | |||||
| chr9:100498945
|
A | G | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.306+71A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100498945 | ||||||
| chr9:100499007
|
T | G | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.306+133T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100499007 | ||||||
| chr9:100499062
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.306+188A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100499062 | ||||||
| chr9:100499391
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.306+517G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100499391 | ||||||
| chr9:100499946
|
G | A | 88 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(85): Show | 88 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.306+1072G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100499946 | ||||||
| chr9:100500252
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(91): Show | 94 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.306+1378T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100500252 | ||||||
| chr9:100500353
|
T | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+1479T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100500353 | ||||||
| chr9:100500360
|
T | A | 1 | a0001c0001t0001g0046 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.306+1486T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100500360 | ||||||
| chr9:100500379
|
C | T | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.306+1505C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100500379 | ||||||
| chr9:100500785
|
A | G | 6 | a0001c0001t0001g0071a0001c0001t0001g0098a0001c0001t0001g0100others(3): Show | 6 | HG00323.hp2 HG01255.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+1911A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100500785 | ||||||
| chr9:100500787
|
A | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.306+1913A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100500787 | ||||||
| chr9:100501033
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.306+2159G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100501033 | ||||||
| chr9:100501098
|
A | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+2224A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100501098 | ||||||
| chr9:100501156
|
G | A | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.306+2282G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100501156 | ||||||
| chr9:100501160
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.306+2286G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100501160 | ||||||
| chr9:100501251
|
G | A | 1 | a0001c0001t0005g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.306+2377G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100501251 | ||||||
| chr9:100501285
|
G | C | 1 | a0001c0001t0001g0047 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.306+2411G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100501285 | ||||||
| chr9:100501470
|
T | C | 5 | a0001c0001t0001g0122a0001c0001t0001g0148a0001c0001t0001g0216others(2): Show | 5 | HG02572.hp1 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+2596T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100501470 | ||||||
| chr9:100501532
|
G | A | 88 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(85): Show | 88 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.306+2658G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100501532 | ||||||
| chr9:100501725
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.306+2851A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100501725 | ||||||
| chr9:100501737
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.306+2863C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100501737 | ||||||
| chr9:100501878
|
C | T | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0003t0001g0127others(6): Show | 9 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.306+3004C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100501878 | ||||||
| chr9:100501879
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.306+3005G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100501879 | ||||||
| chr9:100502782
|
C | G | 10 | a0001c0001t0001g0099a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 10 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.306+3908C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100502782 | ||||||
| chr9:100502822
|
G | C | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.306+3948G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100502822 | ||||||
| chr9:100503013
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.306+4139T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100503013 | ||||||
| chr9:100503078
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.306+4204C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100503078 | ||||||
| chr9:100503285
|
T | C | 3 | a0001c0001t0004g0101a0001c0001t0004g0102a0001c0001t0004g0103 | 3 | NA18942.hp2 NA19000.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.306+4411T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100503285 | ||||||
| chr9:100503479
|
G | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+4605G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100503479 | ||||||
| chr9:100503534
|
AAAC | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0002g0184 | 3 | HG02071.hp1 HG02071.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.306+4662_306+4664d others(5): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100503534 | |||||
| chr9:100503535
|
A | AAC | 24 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0092others(21): Show | 24 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.306+4702_306+4703d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100503535 | |||||
| chr9:100503535
|
A | AACAC | 8 | a0001c0001t0001g0022a0001c0001t0001g0121a0001c0001t0001g0212others(5): Show | 8 | HG02055.hp2 HG03041.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.306+4700_306+4703d others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100503535 | |||||
| chr9:100503535
|
A | AACACAC | 4 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0213others(1): Show | 4 | HG00323.hp1 HG00733.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+4698_306+4703d others(8): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100503535 | |||||
| chr9:100503535
|
A | AC | 5 | a0001c0001t0001g0056a0001c0001t0001g0106a0001c0001t0001g0120others(2): Show | 5 | HG01109.hp1 HG01109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+4661_306+4662i others(3): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100503535 | ||||||
| chr9:100503535
|
AAC | A | 40 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0071others(37): Show | 40 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.306+4702_306+4703d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100503535 | |||||
| chr9:100503535
|
AACAC | A | 61 | a0001c0001t0001g0004a0001c0001t0001g0220a0001c0001t0001g0226others(58): Show | 61 | HG00423.hp1 HG00438.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.306+4700_306+4703d others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100503535 | |||||
| chr9:100503535
|
AACACAC | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(8): Show | 11 | HG00544.hp1 HG01081.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.306+4698_306+4703d others(8): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100503535 | |||||
| chr9:100503535
|
AACACACA others(1): Show |
A | 40 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(37): Show | 40 | HG00423.hp2 HG00733.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.306+4696_306+4703d others(10): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100503535 | |||||
| chr9:100503535
|
AACACACA others(3): Show |
A | 2 | a0001c0001t0001g0041a0001c0001t0001g0064 | 2 | HG00408.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.306+4694_306+4703d others(12): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100503535 | |||||
| chr9:100503710
|
G | A | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.306+4836G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100503710 | ||||||
| chr9:100503977
|
G | T | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0003t0001g0127others(6): Show | 9 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-5028G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100503977 | ||||||
| chr9:100504881
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.307-4124C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100504881 | ||||||
| chr9:100505121
|
A | C | 1 | a0001c0001t0003g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.307-3884A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100505121 | ||||||
| chr9:100505135
|
C | T | 3 | a0001c0001t0004g0101a0001c0001t0004g0102a0001c0001t0004g0103 | 3 | NA18942.hp2 NA19000.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.307-3870C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100505135 | ||||||
| chr9:100505189
|
G | A | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.307-3816G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100505189 | ||||||
| chr9:100505271
|
G | A | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.307-3734G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100505271 | ||||||
| chr9:100505343
|
C | T | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0003t0001g0127others(6): Show | 9 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-3662C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100505343 | ||||||
| chr9:100505410
|
C | CA | 12 | a0001c0001t0001g0051a0001c0001t0001g0094a0001c0001t0001g0117others(9): Show | 12 | HG01192.hp2 HG02004.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.307-3564dupA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100505410 | |||||
| chr9:100505410
|
CA | C | 94 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0024others(91): Show | 94 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.307-3564delA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100505410 | |||||
| chr9:100505410
|
CAA | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(78): Show | 81 | HG00408.hp2 HG00544.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.307-3565_307-3564d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100505410 | |||||
| chr9:100505410
|
CAAA | C | 6 | a0001c0001t0001g0002a0001c0001t0002g0188a0001c0001t0002g0189others(3): Show | 6 | HG01081.hp1 HG01081.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-3566_307-3564d others(5): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100505410 | |||||
| chr9:100505439
|
A | C | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.307-3566A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100505439 | ||||||
| chr9:100505441
|
A | C | 1 | a0001c0001t0001g0021 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.307-3564A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100505441 | ||||||
| chr9:100505459
|
A | T | 1 | a0001c0001t0005g0158 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.307-3546A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100505459 | ||||||
| chr9:100505598
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.307-3407G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100505598 | ||||||
| chr9:100505735
|
C | T | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.307-3270C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100505735 | ||||||
| chr9:100505924
|
G | T | 88 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(85): Show | 88 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.307-3081G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100505924 | ||||||
| chr9:100506085
|
T | C | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0003t0001g0127others(6): Show | 9 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-2920T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100506085 | ||||||
| chr9:100506161
|
G | A | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0003t0001g0127others(6): Show | 9 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-2844G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100506161 | ||||||
| chr9:100506766
|
C | CA | 16 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(13): Show | 16 | HG00438.hp2 HG00738.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.307-2217dupA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100506766 | |||||
| chr9:100506766
|
C | CAA | 46 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(43): Show | 46 | HG00408.hp2 HG00544.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.307-2218_307-2217d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100506766 | |||||
| chr9:100506766
|
C | CAAA | 5 | a0001c0001t0002g0170a0001c0001t0002g0192a0001c0001t0002g0196others(2): Show | 5 | HG00438.hp1 HG04115.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-2219_307-2217d others(5): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100506766 | |||||
| chr9:100506766
|
CA | C | 8 | a0001c0001t0001g0040a0001c0001t0001g0054a0001c0001t0001g0065others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.307-2217delA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100506766 | |||||
| chr9:100507030
|
C | T | 1 | a0001c0001t0002g0192 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.307-1975C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100507030 | ||||||
| chr9:100507225
|
G | A | 89 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(86): Show | 89 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.307-1780G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100507225 | ||||||
| chr9:100507275
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.307-1730A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100507275 | ||||||
| chr9:100507414
|
A | C | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.307-1591A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100507414 | ||||||
| chr9:100507473
|
A | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-1532A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100507473 | ||||||
| chr9:100507535
|
A | G | 1 | a0001c0001t0001g0217 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.307-1470A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100507535 | ||||||
| chr9:100507752
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.307-1253G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100507752 | ||||||
| chr9:100507775
|
T | A | 1 | a0001c0001t0001g0054 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.307-1230T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100507775 | ||||||
| chr9:100508007
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.307-998C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100508007 | ||||||
| chr9:100508033
|
A | G | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.307-972A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100508033 | ||||||
| chr9:100508107
|
G | A | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.307-898G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100508107 | ||||||
| chr9:100508163
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.307-842C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100508163 | ||||||
| chr9:100508246
|
A | C | 1 | a0001c0001t0001g0113 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.307-759A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100508246 | ||||||
| chr9:100508497
|
G | GT | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.307-500dupT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100508497 | |||||
| chr9:100508497
|
G | T | 1 | a0001c0001t0001g0072 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.307-508G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100508497 | ||||||
| chr9:100508834
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-171A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100508834 | ||||||
| chr9:100508865
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.307-140T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100508865 | ||||||
| chr9:100508871
|
C | CA | 33 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(30): Show | 33 | HG00733.hp2 HG01081.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.307-119dupA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100508871 | |||||
| chr9:100508871
|
CA | C | 18 | a0001c0001t0001g0024a0001c0001t0001g0137a0001c0001t0002g0161others(15): Show | 18 | HG02056.hp2 HG02135.hp1 HG02735.hp2 others(15): Show |
intron_variant | MODIFIER | c.307-119delA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 100508871 | |||||
| chr9:100508887
|
C | A | 3 | a0001c0001t0004g0101a0001c0001t0004g0102a0001c0001t0004g0103 | 3 | NA18942.hp2 NA19000.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.307-118C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100508887 | ||||||
| chr9:100508902
|
T | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-103T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 2/9 | chr9 | 100508902 | ||||||
| chr9:100509267
|
A | C | 1 | a0001c0001t0001g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.436+133A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100509267 | ||||||
| chr9:100509319
|
G | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0143 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.436+185G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100509319 | ||||||
| chr9:100509350
|
T | C | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.436+216T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100509350 | ||||||
| chr9:100509477
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.436+343A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100509477 | ||||||
| chr9:100509553
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(91): Show | 94 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.436+419T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100509553 | ||||||
| chr9:100509641
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.436+507G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100509641 | ||||||
| chr9:100509691
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.436+557G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100509691 | ||||||
| chr9:100509775
|
G | GA | 41 | a0001c0001t0001g0019a0001c0001t0001g0063a0001c0001t0001g0238others(38): Show | 41 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.436+657dupA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 100509775 | |||||
| chr9:100509781
|
A | AG | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+647_436+648ins others(1): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100509781 | ||||||
| chr9:100509811
|
A | C | 1 | a0001c0001t0001g0038 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.436+677A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100509811 | ||||||
| chr9:100510048
|
G | C | 88 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(85): Show | 88 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.436+914G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100510048 | ||||||
| chr9:100510268
|
C | T | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.436+1134C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100510268 | ||||||
| chr9:100510395
|
A | T | 1 | a0001c0001t0002g0156 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.436+1261A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100510395 | ||||||
| chr9:100510885
|
A | G | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG02886.hp1 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+1751A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100510885 | ||||||
| chr9:100510956
|
A | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.436+1822A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100510956 | ||||||
| chr9:100510996
|
T | A | 3 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157 | 3 | HG00408.hp2 NA19003.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.436+1862T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100510996 | ||||||
| chr9:100511121
|
T | C | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 12 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+1987T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100511121 | ||||||
| chr9:100511122
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.436+1988G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100511122 | ||||||
| chr9:100511328
|
G | T | 5 | a0001c0001t0002g0159a0001c0001t0002g0160a0001c0001t0002g0197others(2): Show | 5 | HG00423.hp1 HG00544.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-1979G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100511328 | ||||||
| chr9:100511487
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 95 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.437-1820A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100511487 | ||||||
| chr9:100511717
|
A | G | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.437-1590A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100511717 | ||||||
| chr9:100511841
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.437-1466G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100511841 | ||||||
| chr9:100511895
|
A | G | 11 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG00408.hp1 HG02080.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.437-1412A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100511895 | ||||||
| chr9:100511948
|
C | T | 11 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(8): Show | 11 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.437-1359C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100511948 | ||||||
| chr9:100511970
|
T | G | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.437-1337T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100511970 | ||||||
| chr9:100512044
|
C | A | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0003t0001g0127others(6): Show | 9 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.437-1263C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100512044 | ||||||
| chr9:100512117
|
A | C | 2 | a0001c0002t0001g0075a0001c0002t0001g0076 | 2 | HG01081.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.437-1190A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100512117 | ||||||
| chr9:100512175
|
C | T | 11 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG00408.hp1 HG02080.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.437-1132C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100512175 | ||||||
| chr9:100512285
|
C | A | 1 | a0001c0001t0008g0209 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.437-1022C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100512285 | ||||||
| chr9:100512325
|
C | A | 1 | a0001c0001t0001g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.437-982C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100512325 | ||||||
| chr9:100513047
|
T | C | 1 | a0001c0001t0002g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.437-260T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 3/9 | chr9 | 100513047 | ||||||
| chr9:100513393
|
CT | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0038others(13): Show | 16 | HG00558.hp2 HG00639.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.463+77delT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 100513393 | |||||
| chr9:100513409
|
T | A | 1 | a0001c0001t0001g0241 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.463+76T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100513409 | ||||||
| chr9:100513410
|
T | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 234 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.463+77T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100513410 | ||||||
| chr9:100513873
|
G | A | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.463+540G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100513873 | ||||||
| chr9:100514314
|
TA | T | 27 | a0001c0001t0001g0242a0001c0001t0002g0179a0001c0002t0001g0020others(24): Show | 27 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.463+995delA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 100514314 | |||||
| chr9:100514379
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.463+1046C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100514379 | ||||||
| chr9:100514430
|
A | G | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.463+1097A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100514430 | ||||||
| chr9:100514559
|
T | TA | 7 | a0001c0001t0001g0122a0001c0001t0001g0148a0001c0001t0001g0214others(4): Show | 7 | HG02572.hp1 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.463+1227dupA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 100514559 | |||||
| chr9:100514628
|
A | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.463+1295A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100514628 | ||||||
| chr9:100514690
|
C | CA | 6 | a0001c0001t0001g0033a0001c0001t0001g0106a0001c0001t0001g0120others(3): Show | 6 | HG01109.hp1 HG01109.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+1374dupA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 100514690 | |||||
| chr9:100514690
|
CA | C | 7 | a0001c0001t0002g0169a0001c0001t0002g0186a0001c0001t0002g0192others(4): Show | 7 | HG02055.hp1 HG02735.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.463+1374delA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 100514690 | |||||
| chr9:100514690
|
CAA | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(84): Show | 87 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.463+1373_463+1374d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 100514690 | |||||
| chr9:100514691
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.463+1358A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100514691 | ||||||
| chr9:100514692
|
A | C | 5 | a0001c0001t0002g0169a0001c0001t0002g0186a0001c0001t0002g0192others(2): Show | 5 | HG02735.hp1 HG03516.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+1359A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100514692 | ||||||
| chr9:100514693
|
A | C | 54 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.463+1360A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100514693 | ||||||
| chr9:100514694
|
A | C | 5 | a0001c0001t0002g0161a0001c0001t0002g0188a0001c0001t0002g0189others(2): Show | 5 | HG02451.hp2 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+1361A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100514694 | ||||||
| chr9:100514824
|
G | A | 1 | a0001c0001t0002g0161 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.463+1491G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100514824 | ||||||
| chr9:100514981
|
C | T | 1 | a0001c0001t0002g0186 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.463+1648C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100514981 | ||||||
| chr9:100515020
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.464-1655A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100515020 | ||||||
| chr9:100515150
|
A | T | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.464-1525A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100515150 | ||||||
| chr9:100515200
|
T | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.464-1475T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100515200 | ||||||
| chr9:100515201
|
T | A | 10 | a0001c0001t0001g0066a0001c0001t0001g0122a0001c0001t0001g0148others(7): Show | 10 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.464-1474T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100515201 | ||||||
| chr9:100515207
|
A | T | 6 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0051others(3): Show | 6 | HG00733.hp1 HG01167.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.464-1468A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100515207 | ||||||
| chr9:100515372
|
T | A | 1 | a0001c0001t0001g0114 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.464-1303T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100515372 | ||||||
| chr9:100515517
|
G | A | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.464-1158G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100515517 | ||||||
| chr9:100515648
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.464-1027T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100515648 | ||||||
| chr9:100515653
|
G | T | 1 | a0001c0001t0001g0049 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.464-1022G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100515653 | ||||||
| chr9:100515799
|
A | AAAAC | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 92 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.464-864_464-861dup others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 100515799 | |||||
| chr9:100515814
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.464-861A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100515814 | ||||||
| chr9:100515815
|
A | C | 2 | a0001c0001t0001g0005a0001c0001t0006g0023 | 2 | HG01934.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.464-860A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100515815 | ||||||
| chr9:100515836
|
A | G | 21 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.464-839A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100515836 | ||||||
| chr9:100516032
|
A | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(103): Show | 106 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.464-643A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100516032 | ||||||
| chr9:100516046
|
C | T | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.464-629C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100516046 | ||||||
| chr9:100516136
|
C | T | 89 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(86): Show | 89 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.464-539C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100516136 | ||||||
| chr9:100516166
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.464-509G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100516166 | ||||||
| chr9:100516407
|
A | G | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.464-268A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 4/9 | chr9 | 100516407 | ||||||
| chr9:100516908
|
A | G | 10 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0094others(7): Show | 10 | HG01255.hp1 HG02486.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.560+137A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100516908 | ||||||
| chr9:100516980
|
C | A | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560+209C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100516980 | ||||||
| chr9:100517011
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0100 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.560+240T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100517011 | ||||||
| chr9:100517059
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+288C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100517059 | ||||||
| chr9:100517353
|
G | A | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.560+582G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100517353 | ||||||
| chr9:100517451
|
G | A | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.560+680G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100517451 | ||||||
| chr9:100517718
|
A | G | 19 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(16): Show | 19 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.560+947A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100517718 | ||||||
| chr9:100517754
|
A | G | 16 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163others(13): Show | 16 | HG02056.hp2 HG02080.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.560+983A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100517754 | ||||||
| chr9:100517850
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.560+1079G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100517850 | ||||||
| chr9:100518179
|
A | G | 89 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(86): Show | 89 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.560+1408A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100518179 | ||||||
| chr9:100518547
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.560+1776A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100518547 | ||||||
| chr9:100518790
|
A | G | 6 | a0001c0001t0001g0033a0001c0001t0001g0049a0001c0001t0001g0050others(3): Show | 6 | HG01928.hp2 HG01934.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+2019A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100518790 | ||||||
| chr9:100518846
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+2075C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100518846 | ||||||
| chr9:100519022
|
G | C | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.560+2251G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100519022 | ||||||
| chr9:100519022
|
GTTA | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.560+2255_560+2257d others(5): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100519022 | |||||
| chr9:100519057
|
G | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+2286G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100519057 | ||||||
| chr9:100519278
|
T | C | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.560+2507T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100519278 | ||||||
| chr9:100519301
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.560+2530G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100519301 | ||||||
| chr9:100519413
|
C | CTAAA | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 95 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.560+2662_560+2665d others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100519413 | |||||
| chr9:100519485
|
A | G | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560+2714A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100519485 | ||||||
| chr9:100519498
|
G | A | 52 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.560+2727G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100519498 | ||||||
| chr9:100519641
|
C | T | 1 | a0001c0001t0002g0161 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.560+2870C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100519641 | ||||||
| chr9:100519647
|
C | CT | 106 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0034others(103): Show | 106 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.560+2905dupT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100519647 | |||||
| chr9:100519647
|
C | CTT | 36 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0108others(33): Show | 36 | HG00438.hp1 HG00544.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.560+2904_560+2905d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100519647 | |||||
| chr9:100519647
|
CT | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0124a0001c0001t0001g0222others(2): Show | 5 | HG01070.hp1 HG02735.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+2905delT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100519647 | |||||
| chr9:100519647
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0137 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.560+2892_560+2905d others(16): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100519647 | |||||
| chr9:100519647
|
CTTTTTTT others(8): Show |
C | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+2891_560+2905d others(17): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100519647 | |||||
| chr9:100519676
|
T | A | 5 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0230others(2): Show | 5 | HG02145.hp1 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+2905T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100519676 | ||||||
| chr9:100519783
|
T | A | 1 | a0001c0001t0001g0114 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.560+3012T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100519783 | ||||||
| chr9:100519953
|
A | C | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560+3182A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100519953 | ||||||
| chr9:100519979
|
A | G | 52 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.560+3208A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100519979 | ||||||
| chr9:100520164
|
T | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 95 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.560+3393T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100520164 | ||||||
| chr9:100520286
|
T | C | 1 | a0001c0001t0002g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.560+3515T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100520286 | ||||||
| chr9:100520796
|
C | G | 1 | a0001c0001t0001g0234 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.560+4025C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100520796 | ||||||
| chr9:100520819
|
G | A | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.560+4048G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100520819 | ||||||
| chr9:100520855
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 95 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.560+4084T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100520855 | ||||||
| chr9:100521132
|
A | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0002 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.560+4361A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100521132 | ||||||
| chr9:100521183
|
G | A | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.560+4412G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100521183 | ||||||
| chr9:100521183
|
G | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA19002.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.560+4412G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100521183 | ||||||
| chr9:100521185
|
G | A | 88 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(85): Show | 88 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.560+4414G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100521185 | ||||||
| chr9:100521457
|
G | T | 1 | a0001c0003t0001g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.560+4686G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100521457 | ||||||
| chr9:100521576
|
A | C | 4 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0001t0002g0190others(1): Show | 4 | HG02451.hp2 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+4805A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100521576 | ||||||
| chr9:100521956
|
C | A | 37 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(34): Show | 37 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.560+5185C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100521956 | ||||||
| chr9:100522033
|
C | T | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.560+5262C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100522033 | ||||||
| chr9:100522062
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.560+5291G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100522062 | ||||||
| chr9:100522430
|
C | CT | 53 | a0001c0001t0001g0028a0001c0001t0001g0043a0001c0001t0001g0053others(50): Show | 53 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.560+5684dupT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100522430 | |||||
| chr9:100522430
|
C | CTT | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0088others(2): Show | 5 | HG01255.hp1 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+5683_560+5684d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100522430 | |||||
| chr9:100522430
|
C | CTTT | 17 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(14): Show | 17 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.560+5682_560+5684d others(5): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100522430 | |||||
| chr9:100522430
|
C | CTTTT | 6 | a0001c0002t0001g0082a0001c0002t0001g0087a0001c0002t0001g0089others(3): Show | 6 | HG00735.hp2 HG01192.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+5681_560+5684d others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100522430 | |||||
| chr9:100522430
|
C | CTTTTTT | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(2): Show | 5 | HG01081.hp1 HG01934.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+5679_560+5684d others(8): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100522430 | |||||
| chr9:100522430
|
CT | C | 6 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0066others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+5684delT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100522430 | |||||
| chr9:100522485
|
C | T | 3 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157 | 3 | HG00408.hp2 NA19003.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.560+5714C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100522485 | ||||||
| chr9:100522523
|
C | T | 54 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(51): Show | 54 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.560+5752C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100522523 | ||||||
| chr9:100522609
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.560+5838G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100522609 | ||||||
| chr9:100522820
|
C | T | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560+6049C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100522820 | ||||||
| chr9:100523015
|
G | A | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560+6244G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100523015 | ||||||
| chr9:100523782
|
C | T | 3 | a0001c0002t0001g0020a0001c0002t0001g0082a0001c0002t0001g0084 | 3 | HG00735.hp2 HG01975.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.560+7011C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100523782 | ||||||
| chr9:100523807
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(91): Show | 94 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.560+7036A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100523807 | ||||||
| chr9:100524150
|
T | TA | 87 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(84): Show | 87 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.560+7391dupA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100524150 | |||||
| chr9:100524183
|
C | T | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.560+7412C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100524183 | ||||||
| chr9:100524587
|
A | T | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0003t0001g0127others(6): Show | 9 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+7816A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100524587 | ||||||
| chr9:100524612
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.560+7841C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100524612 | ||||||
| chr9:100524677
|
TA | T | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0094others(6): Show | 9 | HG01255.hp1 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.560+7908delA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100524677 | |||||
| chr9:100524681
|
TG | T | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0094others(6): Show | 9 | HG01255.hp1 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.560+7911delG | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100524681 | ||||||
| chr9:100524683
|
A | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0094others(6): Show | 9 | HG01255.hp1 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.560+7912A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100524683 | ||||||
| chr9:100524684
|
G | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0094others(6): Show | 9 | HG01255.hp1 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.560+7913G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100524684 | ||||||
| chr9:100524693
|
G | A | 5 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0230others(2): Show | 5 | HG02145.hp1 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+7922G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100524693 | ||||||
| chr9:100524703
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.560+7932C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100524703 | ||||||
| chr9:100524738
|
A | T | 2 | a0001c0001t0003g0016a0001c0001t0003g0017 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.560+7967A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100524738 | ||||||
| chr9:100524788
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.560+8017A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100524788 | ||||||
| chr9:100524855
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.560+8084T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100524855 | ||||||
| chr9:100524914
|
C | G | 2 | a0001c0001t0004g0101a0001c0001t0004g0103 | 2 | NA18942.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.560+8143C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100524914 | ||||||
| chr9:100525369
|
C | T | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.560+8598C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100525369 | ||||||
| chr9:100525403
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 107 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.560+8632T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100525403 | ||||||
| chr9:100525550
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.560+8779G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100525550 | ||||||
| chr9:100525568
|
C | T | 6 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0051others(3): Show | 6 | HG00733.hp1 HG01167.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+8797C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100525568 | ||||||
| chr9:100525774
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0001g0154 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.560+9003T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100525774 | ||||||
| chr9:100525907
|
G | GTC | 37 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(34): Show | 37 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.560+9145_560+9146d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100525907 | |||||
| chr9:100525911
|
C | G | 4 | a0001c0001t0001g0213a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+9140C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100525911 | ||||||
| chr9:100525929
|
A | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG01255.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.560+9158A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100525929 | ||||||
| chr9:100526058
|
G | A | 21 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.560+9287G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100526058 | ||||||
| chr9:100526300
|
C | T | 6 | a0001c0001t0001g0033a0001c0001t0001g0049a0001c0001t0001g0050others(3): Show | 6 | HG01928.hp2 HG01934.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+9529C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100526300 | ||||||
| chr9:100526322
|
TC | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+9553delC | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100526322 | |||||
| chr9:100526655
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.560+9884T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100526655 | ||||||
| chr9:100526777
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.560+10006G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100526777 | ||||||
| chr9:100526861
|
A | G | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.560+10090A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100526861 | ||||||
| chr9:100526892
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.560+10121C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100526892 | ||||||
| chr9:100526897
|
A | T | 1 | a0001c0001t0001g0057 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.560+10126A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100526897 | ||||||
| chr9:100526927
|
T | C | 88 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(85): Show | 88 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.560+10156T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100526927 | ||||||
| chr9:100526938
|
T | C | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.560+10167T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100526938 | ||||||
| chr9:100526955
|
C | CA | 56 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(53): Show | 56 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.560+10210dupA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100526955 | |||||
| chr9:100526955
|
C | CAA | 17 | a0001c0001t0001g0094a0001c0001t0001g0123a0001c0001t0001g0124others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.560+10209_560+1021 others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100526955 | |||||
| chr9:100526955
|
CA | C | 16 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0069others(13): Show | 16 | HG01934.hp1 HG01952.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.560+10210delA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100526955 | |||||
| chr9:100526955
|
CAAA | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+10208_560+1021 others(7): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100526955 | |||||
| chr9:100526991
|
A | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.560+10220A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100526991 | ||||||
| chr9:100527000
|
G | A | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.560+10229G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527000 | ||||||
| chr9:100527074
|
C | T | 3 | a0001c0002t0001g0089a0001c0002t0001g0091a0001c0003t0001g0127 | 3 | HG01243.hp1 HG01891.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.560+10303C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527074 | ||||||
| chr9:100527248
|
C | T | 22 | a0001c0001t0001g0056a0001c0001t0001g0071a0001c0001t0001g0088others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.560+10477C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527248 | ||||||
| chr9:100527265
|
G | C | 2 | a0001c0001t0001g0208a0001c0001t0008g0209 | 2 | HG02056.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.560+10494G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527265 | ||||||
| chr9:100527382
|
C | T | 88 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(85): Show | 88 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.560+10611C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527382 | ||||||
| chr9:100527392
|
G | A | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0229 | 3 | HG00438.hp2 HG00544.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.560+10621G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527392 | ||||||
| chr9:100527423
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+10652C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527423 | ||||||
| chr9:100527536
|
C | A | 1 | a0001c0001t0002g0177 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.560+10765C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527536 | ||||||
| chr9:100527591
|
C | T | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560+10820C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527591 | ||||||
| chr9:100527652
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+10881C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527652 | ||||||
| chr9:100527670
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 95 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.560+10899A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527670 | ||||||
| chr9:100527719
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+10948C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527719 | ||||||
| chr9:100527841
|
G | A | 89 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(86): Show | 89 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.560+11070G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527841 | ||||||
| chr9:100527856
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.560+11085C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527856 | ||||||
| chr9:100527900
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 108 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.560+11129A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527900 | ||||||
| chr9:100527922
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01934.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.560+11151G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527922 | ||||||
| chr9:100527969
|
A | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 95 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.560+11198A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100527969 | ||||||
| chr9:100528027
|
C | G | 1 | a0001c0001t0001g0033 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.560+11256C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100528027 | ||||||
| chr9:100528204
|
A | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.560+11433A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100528204 | ||||||
| chr9:100528326
|
C | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0148 | 2 | HG01928.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.560+11555C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100528326 | ||||||
| chr9:100528353
|
G | C | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.560+11582G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100528353 | ||||||
| chr9:100528408
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 108 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.560+11637G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100528408 | ||||||
| chr9:100528553
|
A | C | 1 | a0001c0001t0001g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.560+11782A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100528553 | ||||||
| chr9:100528894
|
C | T | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.560+12123C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100528894 | ||||||
| chr9:100529038
|
T | C | 12 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(9): Show | 12 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+12267T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529038 | ||||||
| chr9:100529096
|
A | G | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0003t0001g0127others(6): Show | 9 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+12325A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529096 | ||||||
| chr9:100529159
|
A | G | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.560+12388A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529159 | ||||||
| chr9:100529188
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.560+12417G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529188 | ||||||
| chr9:100529213
|
C | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.560+12442C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529213 | ||||||
| chr9:100529399
|
C | G | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0003t0001g0127others(6): Show | 9 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+12628C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529399 | ||||||
| chr9:100529535
|
G | C | 3 | a0001c0001t0004g0101a0001c0001t0004g0102a0001c0001t0004g0103 | 3 | NA18942.hp2 NA19000.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.560+12764G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529535 | ||||||
| chr9:100529671
|
G | T | 21 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.560+12900G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529671 | ||||||
| chr9:100529694
|
A | G | 4 | a0001c0001t0001g0095a0001c0001t0001g0119a0001c0001t0001g0123others(1): Show | 4 | HG02145.hp2 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+12923A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529694 | ||||||
| chr9:100529729
|
T | A | 1 | a0001c0001t0004g0102 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.560+12958T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529729 | ||||||
| chr9:100529739
|
G | A | 1 | a0001c0002t0001g0020 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.560+12968G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529739 | ||||||
| chr9:100529830
|
C | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+13059C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529830 | ||||||
| chr9:100529836
|
G | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 95 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.560+13065G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529836 | ||||||
| chr9:100529885
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.560+13114C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529885 | ||||||
| chr9:100529951
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.560+13180G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529951 | ||||||
| chr9:100529952
|
A | C | 3 | a0001c0001t0001g0060a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG02027.hp1 HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.560+13181A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529952 | ||||||
| chr9:100529996
|
G | A | 52 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.560+13225G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100529996 | ||||||
| chr9:100530045
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.560+13274C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100530045 | ||||||
| chr9:100530081
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.560+13310C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100530081 | ||||||
| chr9:100530177
|
A | G | 52 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.560+13406A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100530177 | ||||||
| chr9:100530303
|
T | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.560+13532T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100530303 | ||||||
| chr9:100530333
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 95 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.560+13562T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100530333 | ||||||
| chr9:100530377
|
G | C | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.560+13606G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100530377 | ||||||
| chr9:100530379
|
C | T | 2 | a0001c0001t0003g0016a0001c0001t0003g0017 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.560+13608C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100530379 | ||||||
| chr9:100530380
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+13609G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100530380 | ||||||
| chr9:100530456
|
A | T | 52 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.560+13685A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100530456 | ||||||
| chr9:100530517
|
C | T | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560+13746C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100530517 | ||||||
| chr9:100530673
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.560+13902A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100530673 | ||||||
| chr9:100530765
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0143 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.560+13994C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100530765 | ||||||
| chr9:100530791
|
A | C | 21 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.560+14020A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100530791 | ||||||
| chr9:100530957
|
A | G | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.560+14186A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100530957 | ||||||
| chr9:100531020
|
T | G | 7 | a0001c0003t0001g0127a0001c0003t0001g0145a0001c0003t0001g0149others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.560+14249T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531020 | ||||||
| chr9:100531038
|
C | G | 89 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(86): Show | 89 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.560+14267C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531038 | ||||||
| chr9:100531165
|
G | A | 5 | a0001c0001t0002g0159a0001c0001t0002g0160a0001c0001t0002g0197others(2): Show | 5 | HG00423.hp1 HG00544.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+14394G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531165 | ||||||
| chr9:100531273
|
A | G | 2 | a0001c0002t0001g0089a0001c0002t0001g0091 | 2 | HG01243.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.560+14502A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531273 | ||||||
| chr9:100531300
|
C | A | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.560+14529C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531300 | ||||||
| chr9:100531345
|
C | T | 21 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.560+14574C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531345 | ||||||
| chr9:100531403
|
A | T | 1 | a0001c0001t0001g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.560+14632A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531403 | ||||||
| chr9:100531407
|
G | A | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.560+14636G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531407 | ||||||
| chr9:100531474
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+14703G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531474 | ||||||
| chr9:100531720
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.560+14949A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531720 | ||||||
| chr9:100531731
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.560+14960A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531731 | ||||||
| chr9:100531737
|
C | G | 21 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.560+14966C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531737 | ||||||
| chr9:100531758
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+14987G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531758 | ||||||
| chr9:100531762
|
A | C | 1 | a0001c0001t0001g0142 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.560+14991A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531762 | ||||||
| chr9:100531774
|
T | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0236 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.560+15003T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531774 | ||||||
| chr9:100531822
|
A | G | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0003t0001g0127others(6): Show | 9 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+15051A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531822 | ||||||
| chr9:100531932
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.560+15161C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531932 | ||||||
| chr9:100531934
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.560+15163C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531934 | ||||||
| chr9:100531936
|
G | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0049a0001c0001t0001g0050others(3): Show | 6 | HG01928.hp2 HG01934.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+15165G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100531936 | ||||||
| chr9:100532039
|
T | C | 3 | a0001c0001t0001g0234a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | NA18949.hp2 NA19003.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.560+15268T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100532039 | ||||||
| chr9:100532095
|
G | A | 52 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.560+15324G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100532095 | ||||||
| chr9:100532195
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.560+15424T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100532195 | ||||||
| chr9:100532286
|
C | T | 3 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014 | 3 | HG01891.hp2 HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.561-15458C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100532286 | ||||||
| chr9:100532302
|
G | A | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.561-15442G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100532302 | ||||||
| chr9:100532405
|
A | T | 1 | a0001c0001t0001g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.561-15339A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100532405 | ||||||
| chr9:100532564
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG00558.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.561-15180C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100532564 | ||||||
| chr9:100532565
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-15179G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100532565 | ||||||
| chr9:100532680
|
C | T | 3 | a0001c0001t0001g0093a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG01496.hp2 HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.561-15064C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100532680 | ||||||
| chr9:100532729
|
C | T | 1 | a0001c0001t0003g0011 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.561-15015C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100532729 | ||||||
| chr9:100532732
|
T | C | 22 | a0001c0001t0001g0056a0001c0001t0001g0071a0001c0001t0001g0088others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.561-15012T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100532732 | ||||||
| chr9:100532789
|
G | A | 4 | a0001c0001t0001g0213a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-14955G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100532789 | ||||||
| chr9:100532968
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.561-14776G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100532968 | ||||||
| chr9:100533021
|
A | C | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.561-14723A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100533021 | ||||||
| chr9:100533098
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.561-14646G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100533098 | ||||||
| chr9:100533190
|
C | T | 4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0067others(1): Show | 4 | HG01934.hp1 HG01978.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-14554C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100533190 | ||||||
| chr9:100533220
|
G | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(91): Show | 94 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.561-14524G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100533220 | ||||||
| chr9:100533262
|
C | A | 1 | a0001c0001t0001g0046 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.561-14482C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100533262 | ||||||
| chr9:100533541
|
C | T | 12 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0206others(9): Show | 12 | HG00733.hp2 HG01891.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.561-14203C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100533541 | ||||||
| chr9:100533750
|
C | T | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.561-13994C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100533750 | ||||||
| chr9:100533758
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.561-13986C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100533758 | ||||||
| chr9:100533799
|
A | T | 6 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0051others(3): Show | 6 | HG00733.hp1 HG01167.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-13945A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100533799 | ||||||
| chr9:100533805
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.561-13939G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100533805 | ||||||
| chr9:100533862
|
G | A | 7 | a0001c0003t0001g0127a0001c0003t0001g0145a0001c0003t0001g0149others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-13882G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100533862 | ||||||
| chr9:100533986
|
G | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028 | 3 | HG00738.hp2 HG01123.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.561-13758G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100533986 | ||||||
| chr9:100534386
|
C | CT | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0094others(6): Show | 9 | HG01255.hp1 HG02486.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-13357dupT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100534386 | |||||
| chr9:100534523
|
C | G | 25 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.561-13221C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100534523 | ||||||
| chr9:100534674
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.561-13070T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100534674 | ||||||
| chr9:100534727
|
A | G | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.561-13017A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100534727 | ||||||
| chr9:100534748
|
A | C | 8 | a0001c0001t0001g0095a0001c0001t0001g0106a0001c0001t0001g0119others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.561-12996A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100534748 | ||||||
| chr9:100534858
|
G | C | 3 | a0001c0001t0001g0144a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG02602.hp1 HG02976.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.561-12886G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100534858 | ||||||
| chr9:100534966
|
G | T | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.561-12778G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100534966 | ||||||
| chr9:100535026
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.561-12718T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100535026 | ||||||
| chr9:100535248
|
C | A | 1 | a0001c0003t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-12496C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100535248 | ||||||
| chr9:100535317
|
C | T | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.561-12427C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100535317 | ||||||
| chr9:100535386
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.561-12358G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100535386 | ||||||
| chr9:100535536
|
C | T | 4 | a0001c0001t0001g0114a0001c0002t0003g0132a0001c0002t0003g0133others(1): Show | 4 | HG03098.hp1 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-12208C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100535536 | ||||||
| chr9:100535756
|
C | T | 2 | a0001c0003t0001g0127a0001c0003t0001g0145 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.561-11988C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100535756 | ||||||
| chr9:100535776
|
A | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(4): Show | 7 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-11968A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100535776 | ||||||
| chr9:100536077
|
C | G | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.561-11667C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100536077 | ||||||
| chr9:100536153
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.561-11591C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100536153 | ||||||
| chr9:100536414
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.561-11330A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100536414 | ||||||
| chr9:100536616
|
C | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(93): Show | 96 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.561-11128C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100536616 | ||||||
| chr9:100536684
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.561-11060T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100536684 | ||||||
| chr9:100536844
|
T | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(93): Show | 96 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.561-10900T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100536844 | ||||||
| chr9:100537029
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.561-10715A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100537029 | ||||||
| chr9:100537096
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.561-10648A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100537096 | ||||||
| chr9:100537153
|
A | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(93): Show | 96 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.561-10591A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100537153 | ||||||
| chr9:100537187
|
A | G | 35 | a0001c0001t0001g0144a0001c0001t0001g0206a0001c0001t0001g0207others(32): Show | 35 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.561-10557A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100537187 | ||||||
| chr9:100537453
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.561-10291A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100537453 | ||||||
| chr9:100537461
|
A | G | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 12 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.561-10283A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100537461 | ||||||
| chr9:100537511
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.561-10233C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100537511 | ||||||
| chr9:100537725
|
CAT | C | 16 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(13): Show | 16 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.561-10018_561-1001 others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100537725 | ||||||
| chr9:100538114
|
G | T | 53 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(50): Show | 53 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.561-9630G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100538114 | ||||||
| chr9:100538420
|
C | G | 1 | a0001c0001t0001g0134 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.561-9324C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100538420 | ||||||
| chr9:100538430
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.561-9314C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100538430 | ||||||
| chr9:100538527
|
G | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(93): Show | 96 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.561-9217G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100538527 | ||||||
| chr9:100538870
|
A | G | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.561-8874A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100538870 | ||||||
| chr9:100538981
|
C | T | 7 | a0001c0003t0001g0127a0001c0003t0001g0145a0001c0003t0001g0149others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-8763C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100538981 | ||||||
| chr9:100539103
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.561-8641G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100539103 | ||||||
| chr9:100539148
|
C | T | 19 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(16): Show | 19 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.561-8596C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100539148 | ||||||
| chr9:100539149
|
G | A | 3 | a0001c0001t0004g0101a0001c0001t0004g0102a0001c0001t0004g0103 | 3 | NA18942.hp2 NA19000.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.561-8595G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100539149 | ||||||
| chr9:100539329
|
C | G | 3 | a0001c0001t0001g0144a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG02602.hp1 HG02976.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.561-8415C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100539329 | ||||||
| chr9:100539355
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.561-8389C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100539355 | ||||||
| chr9:100539362
|
C | A | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.561-8382C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100539362 | ||||||
| chr9:100539399
|
G | C | 1 | a0001c0001t0001g0219 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.561-8345G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100539399 | ||||||
| chr9:100539421
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.561-8323G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100539421 | ||||||
| chr9:100539478
|
C | T | 1 | a0001c0001t0002g0192 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.561-8266C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100539478 | ||||||
| chr9:100539841
|
A | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-7903A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100539841 | ||||||
| chr9:100539872
|
T | A | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.561-7872T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100539872 | ||||||
| chr9:100540195
|
C | G | 1 | a0001c0002t0001g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561-7549C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100540195 | ||||||
| chr9:100540350
|
C | T | 1 | a0001c0001t0003g0011 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.561-7394C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100540350 | ||||||
| chr9:100540423
|
C | A | 1 | a0001c0002t0001g0090 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.561-7321C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100540423 | ||||||
| chr9:100540476
|
C | T | 7 | a0001c0003t0001g0127a0001c0003t0001g0145a0001c0003t0001g0149others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-7268C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100540476 | ||||||
| chr9:100540713
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.561-7031T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100540713 | ||||||
| chr9:100540751
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(94): Show | 97 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.561-6993T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100540751 | ||||||
| chr9:100540781
|
G | A | 32 | a0001c0001t0001g0137a0001c0002t0001g0020a0001c0002t0001g0073others(29): Show | 32 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.561-6963G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100540781 | ||||||
| chr9:100540832
|
A | G | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.561-6912A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100540832 | ||||||
| chr9:100540855
|
T | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.561-6889T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100540855 | ||||||
| chr9:100540979
|
A | G | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.561-6765A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100540979 | ||||||
| chr9:100541271
|
C | T | 32 | a0001c0001t0001g0137a0001c0002t0001g0020a0001c0002t0001g0073others(29): Show | 32 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.561-6473C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100541271 | ||||||
| chr9:100541347
|
C | CG | 48 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(45): Show | 48 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.561-6397_561-6396i others(3): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100541347 | ||||||
| chr9:100541347
|
C | CGT | 6 | a0001c0001t0002g0168a0001c0001t0002g0179a0001c0001t0002g0197others(3): Show | 6 | HG01952.hp1 HG02135.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-6397_561-6396i others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100541347 | ||||||
| chr9:100541347
|
CA | C | 19 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(16): Show | 19 | HG01081.hp1 HG01243.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.561-6396delA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100541347 | ||||||
| chr9:100541348
|
A | G | 37 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0137others(34): Show | 37 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.561-6396A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100541348 | ||||||
| chr9:100541348
|
A | T | 54 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.561-6396A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100541348 | ||||||
| chr9:100541349
|
T | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(16): Show | 19 | HG01081.hp1 HG01243.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.561-6395T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100541349 | ||||||
| chr9:100541375
|
C | CT | 51 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.561-6353dupT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100541375 | |||||
| chr9:100541435
|
G | A | 52 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.561-6309G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100541435 | ||||||
| chr9:100541875
|
C | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.561-5869C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100541875 | ||||||
| chr9:100542044
|
A | T | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.561-5700A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100542044 | ||||||
| chr9:100542204
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.561-5540C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100542204 | ||||||
| chr9:100542261
|
A | G | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.561-5483A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100542261 | ||||||
| chr9:100542515
|
A | C | 52 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.561-5229A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100542515 | ||||||
| chr9:100542525
|
G | T | 90 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0137others(87): Show | 90 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.561-5219G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100542525 | ||||||
| chr9:100542559
|
C | T | 38 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0137others(35): Show | 38 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.561-5185C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100542559 | ||||||
| chr9:100542586
|
G | A | 4 | a0001c0001t0001g0144a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02602.hp1 HG02976.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-5158G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100542586 | ||||||
| chr9:100542738
|
A | T | 3 | a0001c0001t0004g0101a0001c0001t0004g0102a0001c0001t0004g0103 | 3 | NA18942.hp2 NA19000.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.561-5006A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100542738 | ||||||
| chr9:100542823
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-4921G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100542823 | ||||||
| chr9:100542877
|
A | G | 4 | a0001c0001t0001g0137a0001c0002t0003g0132a0001c0002t0003g0133others(1): Show | 4 | HG02895.hp2 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-4867A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100542877 | ||||||
| chr9:100542923
|
C | CT | 5 | a0001c0001t0001g0061a0001c0001t0001g0235a0001c0001t0002g0182others(2): Show | 5 | HG02027.hp2 HG03492.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-4799dupT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100542923 | |||||
| chr9:100542923
|
CT | C | 54 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0043others(51): Show | 54 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.561-4799delT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100542923 | |||||
| chr9:100542923
|
CTT | C | 21 | a0001c0001t0001g0118a0001c0002t0001g0020a0001c0002t0001g0073others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.561-4800_561-4799d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100542923 | |||||
| chr9:100542925
|
T | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0233 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.561-4819T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100542925 | ||||||
| chr9:100542997
|
T | G | 5 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG00558.hp1 HG01192.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-4747T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100542997 | ||||||
| chr9:100543292
|
T | C | 2 | a0001c0001t0004g0107a0001c0001t0004g0109 | 2 | HG02132.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.561-4452T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100543292 | ||||||
| chr9:100543320
|
C | T | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.561-4424C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100543320 | ||||||
| chr9:100543351
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-4393C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100543351 | ||||||
| chr9:100543354
|
A | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-4390A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100543354 | ||||||
| chr9:100543453
|
A | T | 91 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0137others(88): Show | 91 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.561-4291A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100543453 | ||||||
| chr9:100543663
|
G | A | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.561-4081G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100543663 | ||||||
| chr9:100543704
|
A | AAAACACA others(1): Show |
3 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004 | 3 | HG01243.hp2 HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.561-4039_561-4038i others(10): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100543704 | |||||
| chr9:100543704
|
A | AAC | 51 | a0001c0001t0001g0019a0001c0001t0001g0048a0001c0001t0001g0051others(48): Show | 51 | HG00558.hp2 HG00733.hp1 HG01123.hp2 others(48): Show |
intron_variant | MODIFIER | c.561-3998_561-3997d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100543704 | |||||
| chr9:100543704
|
A | AACAC | 37 | a0001c0001t0001g0026a0001c0001t0001g0044a0001c0001t0001g0071others(34): Show | 37 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.561-4000_561-3997d others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100543704 | |||||
| chr9:100543704
|
A | AACACAC | 12 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0088others(9): Show | 12 | HG01928.hp1 HG02572.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.561-4002_561-3997d others(8): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100543704 | |||||
| chr9:100543704
|
A | AACACACA others(1): Show |
6 | a0001c0001t0001g0093a0001c0001t0001g0137a0001c0001t0001g0206others(3): Show | 6 | HG01496.hp2 HG01952.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-4004_561-3997d others(10): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100543704 | |||||
| chr9:100543704
|
AAC | A | 43 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0045others(40): Show | 43 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.561-3998_561-3997d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100543704 | |||||
| chr9:100543704
|
AACAC | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0060others(3): Show | 6 | HG01109.hp1 HG02027.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-4000_561-3997d others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100543704 | |||||
| chr9:100543704
|
AACACACA others(3): Show |
A | 1 | a0001c0001t0002g0166 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.561-4006_561-3997d others(12): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100543704 | |||||
| chr9:100543968
|
A | T | 14 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0051others(11): Show | 14 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.561-3776A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100543968 | ||||||
| chr9:100544087
|
G | GAT | 54 | a0001c0001t0001g0058a0001c0001t0001g0139a0001c0001t0001g0219others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.561-3639_561-3638d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100544087 | |||||
| chr9:100544087
|
G | GATAT | 25 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(22): Show | 25 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.561-3641_561-3638d others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100544087 | |||||
| chr9:100544087
|
G | GATATATA others(1): Show |
7 | a0001c0003t0001g0127a0001c0003t0001g0145a0001c0003t0001g0149others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-3645_561-3638d others(10): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100544087 | |||||
| chr9:100544241
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0236 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.561-3503A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100544241 | ||||||
| chr9:100544287
|
G | C | 1 | a0001c0002t0001g0090 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.561-3457G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100544287 | ||||||
| chr9:100544509
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0143 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.561-3235G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100544509 | ||||||
| chr9:100545078
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG01255.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.561-2666C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100545078 | ||||||
| chr9:100545359
|
G | C | 1 | a0001c0001t0001g0064 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.561-2385G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100545359 | ||||||
| chr9:100545371
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.561-2373G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100545371 | ||||||
| chr9:100545543
|
A | C | 1 | a0001c0001t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.561-2201A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100545543 | ||||||
| chr9:100545563
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0038 | 2 | NA19004.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.561-2181C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100545563 | ||||||
| chr9:100546120
|
G | C | 4 | a0001c0001t0001g0213a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-1624G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100546120 | ||||||
| chr9:100546191
|
C | T | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.561-1553C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100546191 | ||||||
| chr9:100546281
|
A | C | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.561-1463A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100546281 | ||||||
| chr9:100546429
|
T | TC | 50 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.561-1306dupC | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 100546429 | |||||
| chr9:100546564
|
T | G | 6 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0144others(3): Show | 6 | HG00733.hp2 HG02602.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-1180T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100546564 | ||||||
| chr9:100546613
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.561-1131C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100546613 | ||||||
| chr9:100546714
|
C | T | 52 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.561-1030C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100546714 | ||||||
| chr9:100546847
|
A | T | 1 | a0001c0001t0001g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.561-897A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100546847 | ||||||
| chr9:100547094
|
C | T | 37 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0144others(34): Show | 37 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.561-650C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100547094 | ||||||
| chr9:100547258
|
C | G | 1 | a0001c0001t0002g0186 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.561-486C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100547258 | ||||||
| chr9:100547276
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG02602.hp1 HG02976.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.561-468G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100547276 | ||||||
| chr9:100547525
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.561-219A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100547525 | ||||||
| chr9:100547545
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0001g0154 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.561-199T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100547545 | ||||||
| chr9:100547633
|
A | C | 4 | a0001c0001t0004g0096a0001c0001t0004g0101a0001c0001t0004g0102others(1): Show | 4 | NA18942.hp2 NA19000.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-111A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100547633 | ||||||
| chr9:100547673
|
C | G | 7 | a0001c0003t0001g0127a0001c0003t0001g0145a0001c0003t0001g0149others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-71C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 5/9 | chr9 | 100547673 | ||||||
| chr9:100548458
|
G | A | 52 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.709+566G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 6/9 | chr9 | 100548458 | ||||||
| chr9:100548509
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.709+617A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 6/9 | chr9 | 100548509 | ||||||
| chr9:100548646
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.709+754C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 6/9 | chr9 | 100548646 | ||||||
| chr9:100548796
|
A | G | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.709+904A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 6/9 | chr9 | 100548796 | ||||||
| chr9:100548838
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.709+946G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 6/9 | chr9 | 100548838 | ||||||
| chr9:100549152
|
G | T | 1 | a0001c0001t0002g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.710-943G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 6/9 | chr9 | 100549152 | ||||||
| chr9:100549300
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.710-795G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 6/9 | chr9 | 100549300 | ||||||
| chr9:100549394
|
G | A | 7 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(4): Show | 7 | HG00558.hp1 HG01192.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.710-701G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 6/9 | chr9 | 100549394 | ||||||
| chr9:100549528
|
A | T | 31 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(28): Show | 31 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.710-567A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 6/9 | chr9 | 100549528 | ||||||
| chr9:100549687
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.710-408A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 6/9 | chr9 | 100549687 | ||||||
| chr9:100549704
|
C | G | 1 | a0001c0001t0002g0192 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.710-391C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 6/9 | chr9 | 100549704 | ||||||
| chr9:100549910
|
T | C | 2 | a0001c0002t0001g0075a0001c0002t0001g0076 | 2 | HG01081.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.710-185T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 6/9 | chr9 | 100549910 | ||||||
| chr9:100550008
|
C | A | 89 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0144others(86): Show | 89 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.710-87C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 6/9 | chr9 | 100550008 | ||||||
| chr9:100550046
|
G | A | 4 | a0001c0001t0001g0144a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02602.hp1 HG02976.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.710-49G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 6/9 | chr9 | 100550046 | ||||||
| chr9:100550226
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.775+66A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100550226 | ||||||
| chr9:100550436
|
T | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.775+276T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100550436 | ||||||
| chr9:100550981
|
C | T | 1 | a0001c0003t0001g0151 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.775+821C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100550981 | ||||||
| chr9:100551024
|
A | G | 1 | a0001c0002t0001g0131 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.775+864A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100551024 | ||||||
| chr9:100551059
|
A | G | 10 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(7): Show | 10 | HG01891.hp2 HG02572.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.775+899A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100551059 | ||||||
| chr9:100551150
|
T | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.775+990T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100551150 | ||||||
| chr9:100551517
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.775+1357C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100551517 | ||||||
| chr9:100551601
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.775+1441A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100551601 | ||||||
| chr9:100551791
|
A | G | 3 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG02451.hp2 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.775+1631A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100551791 | ||||||
| chr9:100552135
|
G | T | 52 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.775+1975G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100552135 | ||||||
| chr9:100552618
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.775+2458C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100552618 | ||||||
| chr9:100552850
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.775+2690A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100552850 | ||||||
| chr9:100552862
|
G | GA | 83 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(80): Show | 83 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.775+2702_775+2703i others(3): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100552862 | ||||||
| chr9:100552862
|
G | GAA | 5 | a0001c0001t0001g0144a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG02602.hp1 HG02976.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.775+2702_775+2703i others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100552862 | ||||||
| chr9:100552863
|
G | A | 90 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0144others(87): Show | 90 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.775+2703G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100552863 | ||||||
| chr9:100552863
|
G | GA | 20 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(17): Show | 20 | HG01081.hp1 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.775+2717dupA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 100552863 | |||||
| chr9:100553015
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.775+2855C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100553015 | ||||||
| chr9:100553089
|
G | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.775+2929G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100553089 | ||||||
| chr9:100553249
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.775+3089A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100553249 | ||||||
| chr9:100553349
|
C | G | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.775+3189C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100553349 | ||||||
| chr9:100553392
|
A | T | 1 | a0001c0001t0004g0109 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.775+3232A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100553392 | ||||||
| chr9:100553560
|
CT | C | 13 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.775+3401delT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100553560 | ||||||
| chr9:100553618
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(3): Show | 6 | HG00738.hp2 HG01123.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.775+3458G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100553618 | ||||||
| chr9:100554395
|
G | T | 1 | a0001c0001t0004g0109 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.775+4235G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100554395 | ||||||
| chr9:100554724
|
G | C | 1 | a0001c0001t0001g0058 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.775+4564G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100554724 | ||||||
| chr9:100554884
|
C | T | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.775+4724C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100554884 | ||||||
| chr9:100555073
|
T | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(3): Show | 6 | HG00738.hp2 HG01123.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.775+4913T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100555073 | ||||||
| chr9:100555162
|
G | GAC | 42 | a0001c0001t0001g0019a0001c0001t0001g0067a0001c0001t0001g0097others(39): Show | 42 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.775+5033_775+5034d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 100555162 | |||||
| chr9:100555162
|
G | GACAC | 42 | a0001c0001t0001g0141a0001c0001t0002g0155a0001c0001t0002g0156others(39): Show | 42 | HG00408.hp2 HG00423.hp1 HG01952.hp1 others(39): Show |
intron_variant | MODIFIER | c.775+5031_775+5034d others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 100555162 | |||||
| chr9:100555162
|
G | GACACAC | 7 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0002g0170others(4): Show | 7 | HG02451.hp2 HG02602.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.775+5029_775+5034d others(8): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 100555162 | |||||
| chr9:100555162
|
GAC | G | 4 | a0001c0001t0001g0056a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.775+5033_775+5034d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 100555162 | |||||
| chr9:100555191
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.775+5031A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100555191 | ||||||
| chr9:100555193
|
A | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG02071.hp2 NA18949.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.775+5033A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100555193 | ||||||
| chr9:100555195
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG02071.hp2 NA18949.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.775+5035G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100555195 | ||||||
| chr9:100555341
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 103 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.775+5181C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100555341 | ||||||
| chr9:100555396
|
G | T | 1 | a0001c0001t0001g0004 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.775+5236G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100555396 | ||||||
| chr9:100555745
|
A | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 118 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.775+5585A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100555745 | ||||||
| chr9:100555847
|
G | A | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.776-5550G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100555847 | ||||||
| chr9:100556443
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.776-4954A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100556443 | ||||||
| chr9:100556593
|
A | T | 1 | a0001c0001t0001g0037 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.776-4804A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100556593 | ||||||
| chr9:100556908
|
C | T | 27 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0051others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.776-4489C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100556908 | ||||||
| chr9:100556941
|
G | A | 9 | a0001c0001t0001g0095a0001c0001t0001g0106a0001c0001t0001g0119others(6): Show | 9 | HG00733.hp2 HG01109.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.776-4456G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100556941 | ||||||
| chr9:100557050
|
T | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.776-4347T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100557050 | ||||||
| chr9:100557246
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 119 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.776-4151A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100557246 | ||||||
| chr9:100557454
|
T | A | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.776-3943T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100557454 | ||||||
| chr9:100557478
|
A | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.776-3919A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100557478 | ||||||
| chr9:100557489
|
G | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 104 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.776-3908G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100557489 | ||||||
| chr9:100557515
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 103 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.776-3882G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100557515 | ||||||
| chr9:100557576
|
C | T | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.776-3821C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100557576 | ||||||
| chr9:100557713
|
C | T | 31 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(28): Show | 31 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.776-3684C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100557713 | ||||||
| chr9:100557830
|
C | CT | 57 | a0001c0001t0001g0064a0001c0001t0001g0069a0001c0001t0002g0155others(54): Show | 57 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.776-3552dupT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 100557830 | |||||
| chr9:100557937
|
A | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.776-3460A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100557937 | ||||||
| chr9:100557947
|
G | C | 32 | a0001c0001t0006g0023a0001c0002t0001g0020a0001c0002t0001g0073others(29): Show | 32 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.776-3450G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100557947 | ||||||
| chr9:100558004
|
A | G | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.776-3393A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100558004 | ||||||
| chr9:100558249
|
C | A | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0182 | 3 | HG02027.hp2 HG02523.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.776-3148C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100558249 | ||||||
| chr9:100558256
|
C | T | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.776-3141C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100558256 | ||||||
| chr9:100558314
|
C | T | 21 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.776-3083C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100558314 | ||||||
| chr9:100558372
|
A | G | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.776-3025A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100558372 | ||||||
| chr9:100558633
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.776-2764C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100558633 | ||||||
| chr9:100558903
|
C | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 103 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.776-2494C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100558903 | ||||||
| chr9:100559288
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.776-2109G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100559288 | ||||||
| chr9:100559530
|
G | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.776-1867G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100559530 | ||||||
| chr9:100559538
|
A | G | 1 | a0001c0002t0001g0130 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.776-1859A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100559538 | ||||||
| chr9:100559562
|
A | G | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.776-1835A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100559562 | ||||||
| chr9:100559589
|
T | G | 31 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(28): Show | 31 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.776-1808T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100559589 | ||||||
| chr9:100559633
|
T | A | 56 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(53): Show | 56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.776-1764T>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100559633 | ||||||
| chr9:100559634
|
ACT | A | 56 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(53): Show | 56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.776-1762_776-1761d others(4): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100559634 | ||||||
| chr9:100559695
|
A | G | 2 | a0001c0002t0001g0075a0001c0002t0001g0076 | 2 | HG01081.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.776-1702A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100559695 | ||||||
| chr9:100559852
|
A | G | 1 | a0001c0001t0004g0102 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.776-1545A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100559852 | ||||||
| chr9:100559896
|
G | T | 5 | a0001c0001t0002g0170a0001c0001t0002g0175a0001c0001t0002g0187others(2): Show | 5 | NA18940.hp1 NA18948.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.776-1501G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100559896 | ||||||
| chr9:100559950
|
GT | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.776-1440delT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 100559950 | |||||
| chr9:100559993
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG01255.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.776-1404G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100559993 | ||||||
| chr9:100560048
|
C | G | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0094others(3): Show | 6 | HG01255.hp1 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.776-1349C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100560048 | ||||||
| chr9:100560077
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA19002.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.776-1320A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100560077 | ||||||
| chr9:100560244
|
A | G | 7 | a0001c0003t0001g0127a0001c0003t0001g0145a0001c0003t0001g0149others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.776-1153A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100560244 | ||||||
| chr9:100560345
|
C | T | 10 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(7): Show | 10 | HG00408.hp1 HG02132.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.776-1052C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100560345 | ||||||
| chr9:100560896
|
A | T | 31 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(28): Show | 31 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.776-501A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100560896 | ||||||
| chr9:100561034
|
C | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0092 | 2 | NA18986.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.776-363C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100561034 | ||||||
| chr9:100561354
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.776-43C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 7/9 | chr9 | 100561354 | ||||||
| chr9:100561639
|
A | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.899+119A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100561639 | ||||||
| chr9:100561701
|
A | T | 7 | a0001c0001t0001g0095a0001c0001t0001g0106a0001c0001t0001g0119others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.899+181A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100561701 | ||||||
| chr9:100561749
|
T | C | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.899+229T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100561749 | ||||||
| chr9:100561764
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(102): Show | 105 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.899+244C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100561764 | ||||||
| chr9:100562112
|
C | T | 55 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.899+592C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100562112 | ||||||
| chr9:100562295
|
C | G | 5 | a0001c0001t0002g0159a0001c0001t0002g0160a0001c0001t0002g0197others(2): Show | 5 | HG00423.hp1 HG00544.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.899+775C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100562295 | ||||||
| chr9:100562428
|
C | T | 31 | a0001c0002t0001g0020a0001c0002t0001g0073a0001c0002t0001g0074others(28): Show | 31 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.899+908C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100562428 | ||||||
| chr9:100562439
|
C | T | 9 | a0001c0001t0001g0095a0001c0001t0001g0106a0001c0001t0001g0119others(6): Show | 9 | HG00733.hp2 HG01109.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.899+919C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100562439 | ||||||
| chr9:100562630
|
G | GTTTGT | 35 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0034others(32): Show | 35 | HG00408.hp1 HG00423.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.899+1150_899+1154d others(7): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 100562630 | |||||
| chr9:100562630
|
GTTTGT | G | 96 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(93): Show | 96 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.899+1150_899+1154d others(7): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 100562630 | |||||
| chr9:100562630
|
GTTTGTTT others(3): Show |
G | 6 | a0001c0001t0001g0046a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG00438.hp2 HG00733.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.899+1145_899+1154d others(12): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 100562630 | |||||
| chr9:100562630
|
GTTTGTTT others(8): Show |
G | 1 | a0001c0001t0001g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.899+1140_899+1154d others(17): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 100562630 | |||||
| chr9:100562630
|
GTTTGTTT others(13): Show |
G | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.899+1135_899+1154d others(22): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 100562630 | |||||
| chr9:100562635
|
T | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0154 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.899+1115T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100562635 | ||||||
| chr9:100563062
|
C | T | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.899+1542C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100563062 | ||||||
| chr9:100563468
|
C | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 118 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.899+1948C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100563468 | ||||||
| chr9:100564034
|
G | T | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.899+2514G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100564034 | ||||||
| chr9:100564185
|
T | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(103): Show | 106 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.899+2665T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100564185 | ||||||
| chr9:100564652
|
A | T | 1 | a0001c0001t0002g0183 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.899+3132A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100564652 | ||||||
| chr9:100564668
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.899+3148G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100564668 | ||||||
| chr9:100564760
|
T | C | 3 | a0001c0001t0002g0168a0001c0001t0002g0186a0001c0001t0005g0193 | 3 | HG02735.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.899+3240T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100564760 | ||||||
| chr9:100564987
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.899+3467T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100564987 | ||||||
| chr9:100565151
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.899+3631G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100565151 | ||||||
| chr9:100565302
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.899+3782C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100565302 | ||||||
| chr9:100565391
|
A | G | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.899+3871A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100565391 | ||||||
| chr9:100565461
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.899+3941C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100565461 | ||||||
| chr9:100565573
|
C | T | 7 | a0001c0001t0001g0095a0001c0001t0001g0106a0001c0001t0001g0119others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.899+4053C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100565573 | ||||||
| chr9:100565911
|
C | T | 55 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.899+4391C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100565911 | ||||||
| chr9:100566105
|
A | T | 1 | a0001c0001t0001g0088 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.899+4585A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100566105 | ||||||
| chr9:100566110
|
G | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00733.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.899+4590G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100566110 | ||||||
| chr9:100566201
|
C | T | 55 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.899+4681C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100566201 | ||||||
| chr9:100566337
|
C | A | 2 | a0001c0002t0001g0075a0001c0002t0001g0076 | 2 | HG01081.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.899+4817C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100566337 | ||||||
| chr9:100566371
|
A | G | 3 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0200 | 3 | HG01070.hp2 HG01975.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.899+4851A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100566371 | ||||||
| chr9:100566542
|
T | C | 1 | a0001c0001t0003g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.899+5022T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100566542 | ||||||
| chr9:100566762
|
T | C | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.899+5242T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100566762 | ||||||
| chr9:100566974
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 104 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.899+5454T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100566974 | ||||||
| chr9:100567098
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.900-5420G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100567098 | ||||||
| chr9:100567125
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.900-5393T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100567125 | ||||||
| chr9:100567161
|
C | A | 7 | a0001c0001t0001g0095a0001c0001t0001g0106a0001c0001t0001g0119others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.900-5357C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100567161 | ||||||
| chr9:100567269
|
A | G | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 12 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.900-5249A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100567269 | ||||||
| chr9:100567337
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.900-5181G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100567337 | ||||||
| chr9:100567357
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.900-5161G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100567357 | ||||||
| chr9:100567504
|
C | T | 1 | a0001c0002t0001g0077 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.900-5014C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100567504 | ||||||
| chr9:100567530
|
C | A | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.900-4988C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100567530 | ||||||
| chr9:100567721
|
C | G | 1 | a0001c0001t0006g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.900-4797C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100567721 | ||||||
| chr9:100567728
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.900-4790A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100567728 | ||||||
| chr9:100567867
|
G | A | 20 | a0001c0001t0001g0019a0001c0001t0003g0007a0001c0001t0003g0008others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.900-4651G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100567867 | ||||||
| chr9:100568247
|
G | T | 15 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(12): Show | 15 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.900-4271G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100568247 | ||||||
| chr9:100568548
|
T | G | 1 | a0001c0001t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.900-3970T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100568548 | ||||||
| chr9:100568595
|
T | TCTTC | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(99): Show | 102 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.900-3910_900-3907d others(6): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 100568595 | |||||
| chr9:100568595
|
T | TCTTCCTT others(5): Show |
39 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0032others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.900-3918_900-3907d others(14): Show |
TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 100568595 | |||||
| chr9:100568859
|
G | A | 18 | a0001c0001t0001g0024a0001c0001t0001g0058a0001c0001t0001g0059others(15): Show | 18 | HG00735.hp1 HG01515.hp1 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.900-3659G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100568859 | ||||||
| chr9:100569123
|
T | C | 59 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(56): Show | 59 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.900-3395T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100569123 | ||||||
| chr9:100569155
|
T | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.900-3363T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100569155 | ||||||
| chr9:100569290
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0237 | 2 | HG02071.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.900-3228A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100569290 | ||||||
| chr9:100569371
|
T | G | 18 | a0001c0001t0001g0024a0001c0001t0001g0058a0001c0001t0001g0059others(15): Show | 18 | HG00735.hp1 HG01515.hp1 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.900-3147T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100569371 | ||||||
| chr9:100569561
|
G | T | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG02886.hp1 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.900-2957G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100569561 | ||||||
| chr9:100570039
|
A | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 144 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.900-2479A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100570039 | ||||||
| chr9:100570203
|
C | T | 55 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.900-2315C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100570203 | ||||||
| chr9:100570433
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.900-2085C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100570433 | ||||||
| chr9:100570530
|
A | G | 61 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.900-1988A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100570530 | ||||||
| chr9:100570651
|
G | GT | 26 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0032others(23): Show | 26 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.900-1858dupT | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 100570651 | |||||
| chr9:100570993
|
A | G | 3 | a0001c0002t0003g0132a0001c0002t0003g0133a0001c0002t0003g0146 | 3 | HG03098.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.900-1525A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100570993 | ||||||
| chr9:100571369
|
TA | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 144 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.900-1147delA | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 100571369 | |||||
| chr9:100571380
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.900-1138A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100571380 | ||||||
| chr9:100571398
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.900-1120G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100571398 | ||||||
| chr9:100571474
|
C | G | 18 | a0001c0001t0001g0024a0001c0001t0001g0058a0001c0001t0001g0059others(15): Show | 18 | HG00735.hp1 HG01515.hp1 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.900-1044C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100571474 | ||||||
| chr9:100571495
|
A | G | 55 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.900-1023A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100571495 | ||||||
| chr9:100571548
|
A | G | 55 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.900-970A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100571548 | ||||||
| chr9:100571583
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG01255.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.900-935C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100571583 | ||||||
| chr9:100572001
|
A | C | 1 | a0001c0001t0002g0160 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.900-517A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100572001 | ||||||
| chr9:100572327
|
C | A | 61 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.900-191C>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 8/9 | chr9 | 100572327 | ||||||
| chr9:100572825
|
G | C | 1 | a0001c0001t0001g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1058+149G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100572825 | ||||||
| chr9:100573192
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1058+516C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100573192 | ||||||
| chr9:100573226
|
C | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(85): Show | 88 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1058+550C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100573226 | ||||||
| chr9:100573253
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1058+577A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100573253 | ||||||
| chr9:100573334
|
G | A | 18 | a0001c0001t0001g0024a0001c0001t0001g0058a0001c0001t0001g0059others(15): Show | 18 | HG00735.hp1 HG01515.hp1 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.1058+658G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100573334 | ||||||
| chr9:100573359
|
G | C | 1 | a0001c0001t0001g0143 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1058+683G>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100573359 | ||||||
| chr9:100573891
|
A | C | 7 | a0001c0003t0001g0127a0001c0003t0001g0145a0001c0003t0001g0149others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1058+1215A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100573891 | ||||||
| chr9:100574019
|
TC | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG01081.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1058+1345delC | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 100574019 | |||||
| chr9:100574115
|
A | T | 22 | a0001c0001t0001g0212a0001c0002t0001g0020a0001c0002t0001g0073others(19): Show | 22 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.1058+1439A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100574115 | ||||||
| chr9:100574600
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1059-1916C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100574600 | ||||||
| chr9:100574828
|
C | G | 18 | a0001c0001t0001g0024a0001c0001t0001g0058a0001c0001t0001g0059others(15): Show | 18 | HG00735.hp1 HG01515.hp1 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.1059-1688C>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100574828 | ||||||
| chr9:100574895
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1059-1621G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100574895 | ||||||
| chr9:100574897
|
A | G | 55 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1059-1619A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100574897 | ||||||
| chr9:100574941
|
C | T | 18 | a0001c0001t0001g0024a0001c0001t0001g0058a0001c0001t0001g0059others(15): Show | 18 | HG00735.hp1 HG01515.hp1 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.1059-1575C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100574941 | ||||||
| chr9:100574982
|
T | G | 1 | a0001c0001t0001g0134 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1059-1534T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100574982 | ||||||
| chr9:100575096
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1059-1420A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100575096 | ||||||
| chr9:100575122
|
T | C | 40 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0032others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1059-1394T>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100575122 | ||||||
| chr9:100575268
|
A | T | 60 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(57): Show | 60 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1059-1248A>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100575268 | ||||||
| chr9:100575272
|
A | C | 1 | a0001c0001t0002g0202 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1059-1244A>C | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100575272 | ||||||
| chr9:100575369
|
C | T | 11 | a0001c0001t0001g0024a0001c0001t0001g0058a0001c0001t0001g0059others(8): Show | 11 | HG00735.hp1 HG01515.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.1059-1147C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100575369 | ||||||
| chr9:100575370
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01934.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1059-1146G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100575370 | ||||||
| chr9:100575523
|
C | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(85): Show | 88 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1059-993C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100575523 | ||||||
| chr9:100575730
|
T | G | 25 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0032others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.1059-786T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100575730 | ||||||
| chr9:100575793
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 144 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1059-723C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100575793 | ||||||
| chr9:100575826
|
C | T | 1 | a0001c0002t0001g0131 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1059-690C>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100575826 | ||||||
| chr9:100575890
|
G | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1059-626G>A | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100575890 | ||||||
| chr9:100575975
|
G | T | 60 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(57): Show | 60 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1059-541G>T | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100575975 | ||||||
| chr9:100576001
|
T | G | 1 | a0001c0002t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1059-515T>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100576001 | ||||||
| chr9:100576288
|
A | G | 2 | a0001c0001t0001g0128a0001c0002t0001g0210 | 2 | HG00733.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1059-228A>G | TMEFF1 | ENSG00000241697.5 | transcript | ENST00000374879.5 | protein_coding | 9/9 | chr9 | 100576288 |