Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84190 |
|---|---|
| ensemblid | ENSG00000127720.8 |
| hgncid | 26228 |
| symbol | METTL25 |
| name | methyltransferase like 25 |
| refseq_nuc | NM_032230.3 |
| refseq_prot | NP_115606.2 |
| ensembl_nuc | ENST00000248306.8 |
| ensembl_prot | ENSP00000248306.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 82358529 |
| end | 82479239 |
| strand | + |
| ver | v1.2 |
| region | chr12:82358529-82479239 |
| region5000 | chr12:82353529-82484239 |
| regionname0 | METTL25_chr12_82358529_82479239 |
| regionname5000 | METTL25_chr12_82353529_82484239 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 603 | 86 | 39 | 17 | 12 | 6 | 12 | 8 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0002 | 1/0 | 603 | 18 | 13 | 2 | 0 | 2 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0003 | 0/0 | 603 | 12 | 2 | 3 | 1 | 2 | 4 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0004 | 0/0 | 603 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0005 | 0/0 | 603 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0006 | 0/0 | 603 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0007 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0008 | 0/1 | 603 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0009 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1812 | 80 | 33 | 17 | 12 | 6 | 12 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| c0002 | 1/0 | 1812 | 13 | 12 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| c0003 | 0/0 | 1812 | 11 | 2 | 3 | 1 | 2 | 3 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| c0004 | 0/0 | 1812 | 7 | 7 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| c0005 | 0/0 | 1812 | 6 | 6 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| c0006 | 0/0 | 1812 | 5 | 1 | 2 | 0 | 2 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| c0007 | 0/0 | 1812 | 3 | 3 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| c0008 | 0/0 | 1812 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| c0009 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| c0010 | 0/1 | 1812 | 1 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| c0011 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| c0012 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 253 | 101 | 43 | 19 | 14 | 8 | 15 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| t0002 | 0/0 | 253 | 27 | 22 | 3 | 0 | 2 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| t0003 | 0/0 | 253 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| t0004 | 0/0 | 253 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1812 | 80 | 33 | 17 | 12 | 6 | 12 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0001c0005 | 0/0 | 1812 | 6 | 6 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0002c0002 | 1/0 | 1812 | 13 | 12 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0002c0006 | 0/0 | 1812 | 5 | 1 | 2 | 0 | 2 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0003c0003 | 0/0 | 1812 | 11 | 2 | 3 | 1 | 2 | 3 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0003c0008 | 0/0 | 1812 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0004c0004 | 0/0 | 1812 | 7 | 7 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0005c0007 | 0/0 | 1812 | 3 | 3 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0006c0012 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0007c0011 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0008c0010 | 0/1 | 1812 | 1 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0009c0009 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2064 | 79 | 33 | 17 | 12 | 6 | 11 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0001c0001t0003 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0001c0005t0001 | 0/0 | 2064 | 6 | 6 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0002c0002t0001 | 1/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0002c0002t0002 | 0/0 | 2064 | 12 | 12 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0002c0006t0002 | 0/0 | 2064 | 4 | 0 | 2 | 0 | 2 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0002c0006t0004 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0003c0003t0001 | 0/0 | 2064 | 9 | 1 | 2 | 1 | 2 | 3 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0003c0003t0002 | 0/0 | 2064 | 2 | 1 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0003c0008t0001 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0004c0004t0002 | 0/0 | 2064 | 7 | 7 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0005c0007t0001 | 0/0 | 2064 | 3 | 3 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0006c0012t0001 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0007c0011t0002 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0008c0010t0001 | 0/1 | 2064 | 1 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| a0009c0009t0002 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | copy fasta | chr12 | 82353529 | 82484239 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0005t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0005t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0005t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0002t0001g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0002t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0006t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0006t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0006t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0006t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0006t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0008t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0004c0004t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0004c0004t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0004c0004t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0004c0004t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0004c0004t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0004c0004t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0004c0004t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0005c0007t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0005c0007t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0005c0007t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0006c0012t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0007c0011t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0008c0010t0001g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0009c0009t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG00099 | hp2 | a0003 | c0003 | t0001 | g0110 | EUR | GBR | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | FIN | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG00738 | hp2 | a0003 | c0003 | t0001 | g0108 | AMR | PUR | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01256 | hp2 | a0002 | c0006 | t0002 | g0100 | AMR | CLM | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0111 | AMR | CLM | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01358 | hp1 | a0003 | c0003 | t0002 | g0112 | AMR | CLM | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01361 | hp1 | a0002 | c0006 | t0002 | g0101 | AMR | CLM | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01516 | hp1 | a0002 | c0006 | t0002 | g0102 | EUR | IBS | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01517 | hp1 | a0002 | c0006 | t0002 | g0103 | EUR | IBS | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0089 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01891 | hp1 | a0003 | c0003 | t0001 | g0107 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02055 | hp1 | a0003 | c0003 | t0002 | g0124 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02083 | hp2 | a0003 | c0003 | t0001 | g0115 | EAS | KHV | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02258 | hp2 | a0004 | c0004 | t0002 | g0093 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02280 | hp1 | a0004 | c0004 | t0002 | g0097 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02523 | hp2 | a0006 | c0012 | t0001 | g0045 | EAS | KHV | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0106 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02630 | hp2 | a0002 | c0006 | t0004 | g0105 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02735 | hp2 | a0003 | c0008 | t0001 | g0117 | SAS | PJL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02809 | hp1 | a0004 | c0004 | t0002 | g0094 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02818 | hp1 | a0004 | c0004 | t0002 | g0096 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02895 | hp1 | a0004 | c0004 | t0002 | g0098 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0001 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02897 | hp2 | a0001 | c0005 | t0001 | g0001 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02976 | hp1 | a0005 | c0007 | t0001 | g0024 | AFR | ESN | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02976 | hp2 | a0004 | c0004 | t0002 | g0095 | AFR | ESN | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | MSL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03139 | hp2 | a0001 | c0005 | t0001 | g0012 | AFR | ESN | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0104 | AFR | MSL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03516 | hp1 | a0005 | c0007 | t0001 | g0046 | AFR | ESN | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0092 | AFR | ESN | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03710 | hp1 | a0003 | c0003 | t0001 | g0116 | SAS | PJL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03927 | hp1 | a0003 | c0003 | t0001 | g0109 | SAS | BEB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | BEB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA18522 | hp1 | a0005 | c0007 | t0001 | g0047 | AFR | YRI | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA18522 | hp2 | a0004 | c0004 | t0002 | g0099 | AFR | YRI | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0069 | AFR | YRI | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0090 | AFR | LWK | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0087 | AFR | LWK | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0085 | AFR | ASW | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ASW | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | TSI | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA20752 | hp2 | a0003 | c0003 | t0001 | g0113 | EUR | TSI | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA20905 | hp1 | a0003 | c0003 | t0001 | g0114 | SAS | GIH | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | GIH | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0088 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0001 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02559 | hp1 | a0007 | c0011 | t0002 | g0066 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0086 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03471 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | MSL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0126 | AFR | USA | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | USA | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | USA | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA21309 | hp2 | a0009 | c0009 | t0002 | g0091 | AFR | LWK | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| homoSapiens_chm13v2 | hp1 | a0008 | c0010 | t0001 | g0075 | REF | REF | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0125 | REF | REF | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:82358678
|
C | G | 1 | a0005 | 3 | HG02976.hp1 HG03516.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.113C>G | p.Thr38Ser | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/12 | 150/2064 | 113/1812 | 38/603 | chr12 | 82358678 | ||
| chr12:82358764
|
T | G | 1 | a0003 | 12 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(9): Show |
missense_variant | MODERATE | c.199T>G | p.Ser67Ala | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/12 | 236/2064 | 199/1812 | 67/603 | chr12 | 82358764 | ||
| chr12:82358780
|
T | G | 1 | a0003 | 12 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(9): Show |
missense_variant | MODERATE | c.215T>G | p.Leu72Arg | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/12 | 252/2064 | 215/1812 | 72/603 | chr12 | 82358780 | ||
| chr12:82398885
|
A | G | 1 | a0006 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.622A>G | p.Thr208Ala | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/12 | 659/2064 | 622/1812 | 208/603 | chr12 | 82398885 | ||
| chr12:82399008
|
C | A | 6 | a0001a0003a0005others(3): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
missense_variant | MODERATE | c.745C>A | p.Gln249Lys | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/12 | 782/2064 | 745/1812 | 249/603 | chr12 | 82399008 | ||
| chr12:82399170
|
G | A | 1 | a0008 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.907G>A | p.Glu303Lys | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/12 | 944/2064 | 907/1812 | 303/603 | chr12 | 82399170 | ||
| chr12:82430950
|
G | T | 2 | a0004a0007 | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
missense_variant | MODERATE | c.1337G>T | p.Trp446Leu | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/12 | 1374/2064 | 1337/1812 | 446/603 | chr12 | 82430950 | ||
| chr12:82476676
|
G | T | 1 | a0009 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1605G>T | p.Glu535Asp | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 10/12 | 1642/2064 | 1605/1812 | 535/603 | chr12 | 82476676 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:82386897
|
A | G | 1 | a0002c0006 | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
synonymous_variant | LOW | c.354A>G | p.Gln118Gln | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/12 | 391/2064 | 354/1812 | 118/603 | chr12 | 82386897 | ||
| chr12:82389889
|
C | T | 8 | a0001c0001a0001c0005a0003c0003others(5): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
synonymous_variant | LOW | c.498C>T | p.Ile166Ile | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/12 | 535/2064 | 498/1812 | 166/603 | chr12 | 82389889 | ||
| chr12:82398887
|
C | T | 1 | a0003c0003 | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
synonymous_variant | LOW | c.624C>T | p.Thr208Thr | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/12 | 661/2064 | 624/1812 | 208/603 | chr12 | 82398887 | ||
| chr12:82399163
|
A | G | 1 | a0003c0003 | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
synonymous_variant | LOW | c.900A>G | p.Pro300Pro | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/12 | 937/2064 | 900/1812 | 300/603 | chr12 | 82399163 | ||
| chr12:82403096
|
C | T | 1 | a0001c0005 | 6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
synonymous_variant | LOW | c.1245C>T | p.His415His | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/12 | 1282/2064 | 1245/1812 | 415/603 | chr12 | 82403096 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:82358554
|
A | C | 1 | a0002c0006t0004 | 1 | HG02630.hp2 | 5_prime_UTR_variant | MODIFIER | c.-12A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/12 | 12 | chr12 | 82358554 | |||||
| chr12:82479095
|
A | G | 1 | a0001c0001t0003 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*71A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 12/12 | 71 | chr12 | 82479095 | |||||
| chr12:82479134
|
G | A | 7 | a0002c0002t0002a0002c0006t0002a0002c0006t0004others(4): Show | 28 | HG01256.hp2 HG01358.hp1 HG01361.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*110G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 12/12 | 110 | chr12 | 82479134 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:82358854
|
G | A | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 83 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.259+30G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82358854 | ||||||
| chr12:82358915
|
A | C | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+91A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82358915 | ||||||
| chr12:82358964
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.259+140G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82358964 | ||||||
| chr12:82359232
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.259+408G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82359232 | ||||||
| chr12:82359302
|
G | GC | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.259+479dupC | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82359302 | |||||
| chr12:82359460
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.259+636C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82359460 | ||||||
| chr12:82359521
|
G | C | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.259+697G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82359521 | ||||||
| chr12:82359571
|
G | C | 1 | a0001c0001t0001g0005 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.259+747G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82359571 | ||||||
| chr12:82359685
|
A | AT | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+866dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82359685 | |||||
| chr12:82359773
|
A | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.259+949A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82359773 | ||||||
| chr12:82359815
|
G | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.259+991G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82359815 | ||||||
| chr12:82359867
|
T | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.259+1043T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82359867 | ||||||
| chr12:82359987
|
T | C | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+1163T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82359987 | ||||||
| chr12:82360283
|
C | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+1459C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82360283 | ||||||
| chr12:82360321
|
T | C | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.259+1497T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82360321 | ||||||
| chr12:82360421
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+1597A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82360421 | ||||||
| chr12:82360520
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.259+1696A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82360520 | ||||||
| chr12:82360579
|
G | T | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.259+1755G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82360579 | ||||||
| chr12:82360602
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.259+1778G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82360602 | ||||||
| chr12:82360700
|
G | A | 4 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090others(1): Show | 4 | HG01884.hp2 HG02109.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+1876G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82360700 | ||||||
| chr12:82360706
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.259+1882A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82360706 | ||||||
| chr12:82360757
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.259+1933C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82360757 | ||||||
| chr12:82360839
|
G | A | 1 | a0001c0005t0001g0007 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.259+2015G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82360839 | ||||||
| chr12:82360848
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+2024A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82360848 | ||||||
| chr12:82360934
|
T | A | 1 | a0001c0001t0001g0004 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.259+2110T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82360934 | ||||||
| chr12:82361010
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.259+2186A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361010 | ||||||
| chr12:82361037
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+2213C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361037 | ||||||
| chr12:82361046
|
C | T | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.259+2222C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361046 | ||||||
| chr12:82361104
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.259+2280C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361104 | ||||||
| chr12:82361143
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.259+2319G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361143 | ||||||
| chr12:82361145
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.259+2321C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361145 | ||||||
| chr12:82361197
|
C | T | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+2373C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361197 | ||||||
| chr12:82361207
|
C | G | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+2383C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361207 | ||||||
| chr12:82361291
|
C | T | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+2467C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361291 | ||||||
| chr12:82361336
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.259+2512G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361336 | ||||||
| chr12:82361357
|
G | C | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+2533G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361357 | ||||||
| chr12:82361368
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.259+2544G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361368 | ||||||
| chr12:82361414
|
C | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+2590C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361414 | ||||||
| chr12:82361475
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.259+2651C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361475 | ||||||
| chr12:82361512
|
G | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.259+2688G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361512 | ||||||
| chr12:82361536
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+2712C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361536 | ||||||
| chr12:82361560
|
C | G | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+2736C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361560 | ||||||
| chr12:82361562
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.259+2738C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361562 | ||||||
| chr12:82361563
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+2739G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361563 | ||||||
| chr12:82361603
|
C | T | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259+2779C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361603 | ||||||
| chr12:82361728
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+2904G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361728 | ||||||
| chr12:82361741
|
C | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 6 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+2917C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361741 | ||||||
| chr12:82361752
|
C | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+2928C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361752 | ||||||
| chr12:82361769
|
C | T | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+2945C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361769 | ||||||
| chr12:82361960
|
G | A | 1 | a0003c0003t0001g0107 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.259+3136G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361960 | ||||||
| chr12:82362019
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.259+3195C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82362019 | ||||||
| chr12:82362196
|
G | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.259+3372G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82362196 | ||||||
| chr12:82362206
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+3382A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82362206 | ||||||
| chr12:82362229
|
T | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.259+3405T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82362229 | ||||||
| chr12:82362263
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.259+3439A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82362263 | ||||||
| chr12:82362336
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.259+3512G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82362336 | ||||||
| chr12:82362619
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.259+3795T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82362619 | ||||||
| chr12:82362645
|
G | A | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+3821G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82362645 | ||||||
| chr12:82363095
|
G | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+4271G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82363095 | ||||||
| chr12:82363195
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.259+4371G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82363195 | ||||||
| chr12:82363296
|
G | A | 1 | a0001c0005t0001g0012 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.259+4472G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82363296 | ||||||
| chr12:82363401
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.259+4577C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82363401 | ||||||
| chr12:82363696
|
C | T | 1 | a0008c0010t0001g0075 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.259+4872C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82363696 | ||||||
| chr12:82363731
|
T | TA | 80 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(77): Show | 81 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.259+4921dupA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82363731 | |||||
| chr12:82363731
|
T | TAA | 5 | a0003c0003t0001g0108a0003c0003t0001g0109a0003c0003t0001g0110others(2): Show | 5 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+4920_259+4921d others(4): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82363731 | |||||
| chr12:82363916
|
T | C | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+5092T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82363916 | ||||||
| chr12:82364176
|
A | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.259+5352A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82364176 | ||||||
| chr12:82364190
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.259+5366A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82364190 | ||||||
| chr12:82364266
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+5442A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82364266 | ||||||
| chr12:82364586
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.259+5762G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82364586 | ||||||
| chr12:82364834
|
T | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | HG00099.hp1 HG01433.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+6010T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82364834 | ||||||
| chr12:82365115
|
A | G | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+6291A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365115 | ||||||
| chr12:82365132
|
G | A | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+6308G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365132 | ||||||
| chr12:82365351
|
C | T | 1 | a0002c0006t0004g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.259+6527C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365351 | ||||||
| chr12:82365352
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.259+6528C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365352 | ||||||
| chr12:82365385
|
C | A | 14 | a0002c0002t0002g0092a0002c0002t0002g0106a0002c0006t0002g0100others(11): Show | 14 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.259+6561C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365385 | ||||||
| chr12:82365417
|
A | G | 10 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(7): Show | 10 | HG02280.hp2 HG02717.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.259+6593A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365417 | ||||||
| chr12:82365420
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+6596A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365420 | ||||||
| chr12:82365427
|
C | T | 1 | a0003c0003t0002g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.259+6603C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365427 | ||||||
| chr12:82365530
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.259+6706A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365530 | ||||||
| chr12:82365580
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.259+6756G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365580 | ||||||
| chr12:82365583
|
A | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+6759A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365583 | ||||||
| chr12:82365648
|
G | A | 1 | a0003c0003t0002g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.259+6824G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365648 | ||||||
| chr12:82365704
|
AGCTAAAA others(103): Show |
A | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+6884_259+6993d others(2): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82365704 | |||||
| chr12:82365763
|
T | A | 1 | a0001c0001t0001g0019 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.259+6939T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365763 | ||||||
| chr12:82365821
|
G | A | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+6997G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365821 | ||||||
| chr12:82365845
|
G | A | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.259+7021G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365845 | ||||||
| chr12:82365950
|
C | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+7126C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82365950 | ||||||
| chr12:82366059
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.259+7235A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82366059 | ||||||
| chr12:82366089
|
T | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.259+7265T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82366089 | ||||||
| chr12:82366102
|
T | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+7278T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82366102 | ||||||
| chr12:82366273
|
T | A | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+7449T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82366273 | ||||||
| chr12:82366291
|
G | T | 5 | a0003c0003t0001g0108a0003c0003t0001g0109a0003c0003t0001g0110others(2): Show | 5 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+7467G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82366291 | ||||||
| chr12:82366429
|
C | T | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+7605C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82366429 | ||||||
| chr12:82366574
|
TA | T | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.259+7751delA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82366574 | ||||||
| chr12:82366575
|
A | AT | 4 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+7763dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82366575 | |||||
| chr12:82366761
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.259+7937G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82366761 | ||||||
| chr12:82366959
|
T | A | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+8135T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82366959 | ||||||
| chr12:82367275
|
A | G | 14 | a0002c0002t0002g0092a0002c0002t0002g0106a0002c0006t0002g0100others(11): Show | 14 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.259+8451A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82367275 | ||||||
| chr12:82367594
|
T | C | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.259+8770T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82367594 | ||||||
| chr12:82367656
|
C | T | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.259+8832C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82367656 | ||||||
| chr12:82367657
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.259+8833A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82367657 | ||||||
| chr12:82367697
|
C | T | 1 | a0008c0010t0001g0075 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.259+8873C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82367697 | ||||||
| chr12:82368030
|
G | A | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+9206G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82368030 | ||||||
| chr12:82368084
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.259+9260C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82368084 | ||||||
| chr12:82368167
|
A | T | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.259+9343A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82368167 | ||||||
| chr12:82368223
|
C | T | 11 | a0001c0001t0001g0053a0003c0003t0001g0107a0003c0003t0001g0108others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+9399C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82368223 | ||||||
| chr12:82368367
|
C | T | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | HG00280.hp1 HG01433.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+9543C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82368367 | ||||||
| chr12:82368661
|
A | T | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.259+9837A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82368661 | ||||||
| chr12:82368711
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.259+9887A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82368711 | ||||||
| chr12:82368769
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.259+9945T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82368769 | ||||||
| chr12:82368808
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.259+9984A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82368808 | ||||||
| chr12:82368813
|
A | G | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.259+9989A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82368813 | ||||||
| chr12:82368819
|
C | T | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+9995C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82368819 | ||||||
| chr12:82369221
|
C | G | 14 | a0002c0002t0002g0092a0002c0002t0002g0106a0002c0006t0002g0100others(11): Show | 14 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.259+10397C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82369221 | ||||||
| chr12:82369330
|
G | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.259+10506G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82369330 | ||||||
| chr12:82369519
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.259+10695A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82369519 | ||||||
| chr12:82369620
|
G | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.259+10796G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82369620 | ||||||
| chr12:82369785
|
TTG | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.259+10962_259+1096 others(6): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82369785 | ||||||
| chr12:82370066
|
C | T | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.259+11242C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82370066 | ||||||
| chr12:82370129
|
G | A | 1 | a0002c0006t0004g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.259+11305G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82370129 | ||||||
| chr12:82370293
|
G | A | 14 | a0002c0002t0002g0092a0002c0002t0002g0106a0002c0006t0002g0100others(11): Show | 14 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.259+11469G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82370293 | ||||||
| chr12:82370700
|
TTCTA | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.259+11880_259+1188 others(8): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82370700 | |||||
| chr12:82370770
|
G | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.259+11946G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82370770 | ||||||
| chr12:82370806
|
C | G | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.259+11982C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82370806 | ||||||
| chr12:82370852
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.259+12028G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82370852 | ||||||
| chr12:82371044
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.259+12220A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82371044 | ||||||
| chr12:82371328
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.259+12504C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82371328 | ||||||
| chr12:82371335
|
C | T | 4 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090others(1): Show | 4 | HG01884.hp2 HG02109.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+12511C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82371335 | ||||||
| chr12:82371409
|
G | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.259+12585G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82371409 | ||||||
| chr12:82371421
|
G | T | 1 | a0001c0001t0001g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.259+12597G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82371421 | ||||||
| chr12:82371780
|
C | T | 2 | a0005c0007t0001g0046a0005c0007t0001g0047 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.259+12956C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82371780 | ||||||
| chr12:82371830
|
C | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.259+13006C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82371830 | ||||||
| chr12:82371887
|
C | T | 8 | a0002c0002t0002g0092a0004c0004t0002g0093a0004c0004t0002g0094others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+13063C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82371887 | ||||||
| chr12:82371916
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.259+13092C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82371916 | ||||||
| chr12:82371937
|
G | T | 1 | a0006c0012t0001g0045 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.259+13113G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82371937 | ||||||
| chr12:82372122
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.259+13298T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82372122 | ||||||
| chr12:82372129
|
C | T | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.259+13305C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82372129 | ||||||
| chr12:82372282
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.259+13458T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82372282 | ||||||
| chr12:82372331
|
T | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.259+13507T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82372331 | ||||||
| chr12:82372401
|
G | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0044 | 2 | HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.259+13577G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82372401 | ||||||
| chr12:82372520
|
A | T | 1 | a0001c0001t0001g0043 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.259+13696A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82372520 | ||||||
| chr12:82372524
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.259+13700C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82372524 | ||||||
| chr12:82372541
|
C | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259+13717C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82372541 | ||||||
| chr12:82372986
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 6 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.260-13817G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82372986 | ||||||
| chr12:82372995
|
C | T | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-13808C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82372995 | ||||||
| chr12:82373037
|
C | A | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.260-13766C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82373037 | ||||||
| chr12:82373134
|
G | A | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-13669G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82373134 | ||||||
| chr12:82373165
|
G | A | 1 | a0002c0002t0002g0088 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.260-13638G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82373165 | ||||||
| chr12:82373212
|
C | G | 1 | a0001c0001t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.260-13591C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82373212 | ||||||
| chr12:82373243
|
A | G | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-13560A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82373243 | ||||||
| chr12:82373252
|
C | T | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.260-13551C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82373252 | ||||||
| chr12:82373294
|
C | A | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.260-13509C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82373294 | ||||||
| chr12:82373347
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-13456C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82373347 | ||||||
| chr12:82373596
|
G | T | 1 | a0001c0001t0001g0042 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.260-13207G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82373596 | ||||||
| chr12:82373635
|
C | T | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-13168C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82373635 | ||||||
| chr12:82373716
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-13087C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82373716 | ||||||
| chr12:82373897
|
G | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.260-12906G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82373897 | ||||||
| chr12:82374064
|
A | C | 1 | a0001c0005t0001g0012 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.260-12739A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82374064 | ||||||
| chr12:82374385
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.260-12418A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82374385 | ||||||
| chr12:82374461
|
C | G | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.260-12342C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82374461 | ||||||
| chr12:82374494
|
G | A | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.260-12309G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82374494 | ||||||
| chr12:82374669
|
A | G | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-12134A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82374669 | ||||||
| chr12:82374791
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.260-12012A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82374791 | ||||||
| chr12:82374798
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.260-12005A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82374798 | ||||||
| chr12:82374888
|
G | T | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.260-11915G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82374888 | ||||||
| chr12:82374938
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-11865A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82374938 | ||||||
| chr12:82374941
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.260-11862G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82374941 | ||||||
| chr12:82375211
|
T | TGATGGTA others(110): Show |
1 | a0002c0006t0002g0100 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.260-11591_260-1147 others(121): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82375211 | |||||
| chr12:82375266
|
A | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-11537A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82375266 | ||||||
| chr12:82375442
|
GA | G | 16 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(13): Show | 17 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.260-11350delA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82375442 | |||||
| chr12:82375450
|
A | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.260-11353A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82375450 | ||||||
| chr12:82375452
|
A | AT | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 87 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.260-11351_260-1135 others(5): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82375452 | ||||||
| chr12:82375452
|
A | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(15): Show | 19 | HG00099.hp2 HG01346.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.260-11351A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82375452 | ||||||
| chr12:82375453
|
AT | A | 7 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-11349delT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82375453 | ||||||
| chr12:82375456
|
T | C | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.260-11347T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82375456 | ||||||
| chr12:82375459
|
A | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.260-11344A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82375459 | ||||||
| chr12:82375463
|
GTTCTT | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-11338_260-1133 others(9): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82375463 | |||||
| chr12:82375544
|
A | G | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-11259A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82375544 | ||||||
| chr12:82375851
|
C | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.260-10952C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82375851 | ||||||
| chr12:82375862
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-10941A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82375862 | ||||||
| chr12:82375921
|
G | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-10882G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82375921 | ||||||
| chr12:82375932
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-10871A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82375932 | ||||||
| chr12:82375934
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0063 | 2 | HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.260-10869G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82375934 | ||||||
| chr12:82376122
|
G | A | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-10681G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82376122 | ||||||
| chr12:82376130
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.260-10673C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82376130 | ||||||
| chr12:82376241
|
C | T | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-10562C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82376241 | ||||||
| chr12:82376280
|
C | T | 12 | a0001c0001t0001g0040a0001c0001t0001g0054a0001c0001t0001g0055others(9): Show | 12 | HG02280.hp2 HG02717.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.260-10523C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82376280 | ||||||
| chr12:82376378
|
T | C | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-10425T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82376378 | ||||||
| chr12:82376414
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.260-10389A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82376414 | ||||||
| chr12:82376418
|
T | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.260-10385T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82376418 | ||||||
| chr12:82376528
|
A | G | 3 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086 | 4 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-10275A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82376528 | ||||||
| chr12:82376705
|
T | C | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-10098T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82376705 | ||||||
| chr12:82376715
|
C | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.260-10088C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82376715 | ||||||
| chr12:82376854
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-9949A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82376854 | ||||||
| chr12:82376970
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.260-9833C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82376970 | ||||||
| chr12:82377086
|
C | G | 14 | a0002c0002t0002g0092a0002c0002t0002g0106a0002c0006t0002g0100others(11): Show | 14 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.260-9717C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82377086 | ||||||
| chr12:82377089
|
G | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-9714G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82377089 | ||||||
| chr12:82377113
|
C | CA | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-9679dupA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82377113 | |||||
| chr12:82377318
|
T | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-9485T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82377318 | ||||||
| chr12:82377386
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.260-9417T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82377386 | ||||||
| chr12:82377462
|
TC | T | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-9340delC | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82377462 | ||||||
| chr12:82377636
|
C | A | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-9167C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82377636 | ||||||
| chr12:82378010
|
A | AT | 5 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(2): Show | 6 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.260-8784dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82378010 | |||||
| chr12:82378021
|
G | A | 1 | a0005c0007t0001g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.260-8782G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82378021 | ||||||
| chr12:82378190
|
C | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0070others(3): Show | 6 | HG01257.hp2 HG01978.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.260-8613C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82378190 | ||||||
| chr12:82378191
|
T | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.260-8612T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82378191 | ||||||
| chr12:82378352
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-8451C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82378352 | ||||||
| chr12:82378508
|
A | G | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-8295A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82378508 | ||||||
| chr12:82378539
|
A | G | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.260-8264A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82378539 | ||||||
| chr12:82378742
|
A | G | 14 | a0002c0002t0002g0092a0002c0002t0002g0106a0002c0006t0002g0100others(11): Show | 14 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.260-8061A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82378742 | ||||||
| chr12:82378753
|
G | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.260-8050G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82378753 | ||||||
| chr12:82378764
|
C | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-8039C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82378764 | ||||||
| chr12:82378816
|
T | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-7987T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82378816 | ||||||
| chr12:82379036
|
GACA | G | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-7760_260-7758d others(5): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82379036 | |||||
| chr12:82379183
|
AT | A | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.260-7616delT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82379183 | |||||
| chr12:82379233
|
C | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0063 | 3 | HG02886.hp1 HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.260-7570C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82379233 | ||||||
| chr12:82379519
|
CTG | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-7282_260-7281d others(4): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82379519 | |||||
| chr12:82379525
|
T | G | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-7278T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82379525 | ||||||
| chr12:82379591
|
G | A | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.260-7212G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82379591 | ||||||
| chr12:82379694
|
C | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-7109C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82379694 | ||||||
| chr12:82379747
|
A | G | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-7056A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82379747 | ||||||
| chr12:82379753
|
A | C | 1 | a0001c0001t0001g0078 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.260-7050A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82379753 | ||||||
| chr12:82379868
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.260-6935A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82379868 | ||||||
| chr12:82380088
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0120 | 3 | HG02572.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.260-6715T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380088 | ||||||
| chr12:82380105
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.260-6698A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380105 | ||||||
| chr12:82380120
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.260-6683T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380120 | ||||||
| chr12:82380203
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.260-6600T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380203 | ||||||
| chr12:82380226
|
C | T | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.260-6577C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380226 | ||||||
| chr12:82380239
|
G | C | 3 | a0003c0003t0001g0107a0003c0003t0001g0113a0003c0003t0001g0114 | 3 | HG01891.hp1 NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.260-6564G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380239 | ||||||
| chr12:82380270
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-6533C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380270 | ||||||
| chr12:82380303
|
A | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.260-6500A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380303 | ||||||
| chr12:82380393
|
C | A | 1 | a0001c0001t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.260-6410C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380393 | ||||||
| chr12:82380405
|
G | A | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.260-6398G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380405 | ||||||
| chr12:82380412
|
A | G | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-6391A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380412 | ||||||
| chr12:82380418
|
T | C | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-6385T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380418 | ||||||
| chr12:82380429
|
GTGTA | G | 2 | a0001c0001t0001g0006a0002c0002t0002g0126 | 2 | HG01361.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.260-6368_260-6365d others(6): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82380429 | |||||
| chr12:82380433
|
ATG | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.260-6368_260-6367d others(4): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82380433 | |||||
| chr12:82380435
|
G | GTA | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.260-6356_260-6355d others(4): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82380435 | |||||
| chr12:82380448
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-6355T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380448 | ||||||
| chr12:82380725
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.260-6078C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380725 | ||||||
| chr12:82380836
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.260-5967T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380836 | ||||||
| chr12:82380862
|
G | C | 5 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(2): Show | 6 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.260-5941G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82380862 | ||||||
| chr12:82381701
|
G | A | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.260-5102G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82381701 | ||||||
| chr12:82381755
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.260-5048G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82381755 | ||||||
| chr12:82381889
|
T | A | 3 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086 | 4 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-4914T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82381889 | ||||||
| chr12:82382344
|
A | C | 1 | a0001c0001t0001g0053 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.260-4459A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82382344 | ||||||
| chr12:82382629
|
A | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-4174A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82382629 | ||||||
| chr12:82382724
|
C | CT | 2 | a0001c0005t0001g0001a0001c0005t0001g0069 | 4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-4070dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82382724 | |||||
| chr12:82382758
|
C | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.260-4045C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82382758 | ||||||
| chr12:82382767
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-4036G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82382767 | ||||||
| chr12:82382854
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-3949A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82382854 | ||||||
| chr12:82382910
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-3893A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82382910 | ||||||
| chr12:82382955
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-3848A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82382955 | ||||||
| chr12:82382997
|
A | G | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-3806A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82382997 | ||||||
| chr12:82383238
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.260-3565G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82383238 | ||||||
| chr12:82383267
|
T | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-3536T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82383267 | ||||||
| chr12:82383270
|
G | A | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-3533G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82383270 | ||||||
| chr12:82383347
|
CTTTG | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.260-3450_260-3447d others(6): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82383347 | |||||
| chr12:82383618
|
G | A | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.260-3185G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82383618 | ||||||
| chr12:82383630
|
G | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.260-3173G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82383630 | ||||||
| chr12:82383819
|
T | C | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.260-2984T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82383819 | ||||||
| chr12:82383993
|
C | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.260-2810C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82383993 | ||||||
| chr12:82384068
|
A | G | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.260-2735A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82384068 | ||||||
| chr12:82384112
|
C | T | 9 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(6): Show | 10 | HG01884.hp2 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-2691C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82384112 | ||||||
| chr12:82384267
|
C | G | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-2536C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82384267 | ||||||
| chr12:82384374
|
G | GCTCT | 6 | a0001c0001t0001g0065a0002c0006t0002g0100a0002c0006t0002g0101others(3): Show | 6 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.260-2410_260-2407d others(6): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82384374 | |||||
| chr12:82384374
|
GCT | G | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.260-2408_260-2407d others(4): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82384374 | |||||
| chr12:82384403
|
C | G | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.260-2400C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82384403 | ||||||
| chr12:82384412
|
T | TC | 8 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0070others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-2385dupC | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82384412 | |||||
| chr12:82384567
|
A | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-2236A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82384567 | ||||||
| chr12:82384602
|
A | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-2201A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82384602 | ||||||
| chr12:82384609
|
C | CT | 10 | a0002c0002t0002g0092a0003c0003t0001g0107a0003c0003t0001g0108others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-2188dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82384609 | |||||
| chr12:82384609
|
C | T | 1 | a0003c0003t0001g0116 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.260-2194C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82384609 | ||||||
| chr12:82384614
|
T | TAA | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-2189_260-2188i others(4): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82384614 | ||||||
| chr12:82384615
|
T | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0084others(4): Show | 8 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-2188T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82384615 | ||||||
| chr12:82384615
|
T | TA | 15 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(12): Show | 16 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.260-2179dupA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82384615 | |||||
| chr12:82384625
|
T | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.260-2178T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82384625 | ||||||
| chr12:82384640
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.260-2163A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82384640 | ||||||
| chr12:82384889
|
C | G | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-1914C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82384889 | ||||||
| chr12:82384952
|
T | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-1851T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82384952 | ||||||
| chr12:82385032
|
A | G | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-1771A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82385032 | ||||||
| chr12:82385115
|
T | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-1688T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82385115 | ||||||
| chr12:82385116
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.260-1687A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82385116 | ||||||
| chr12:82385150
|
A | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.260-1653A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82385150 | ||||||
| chr12:82385198
|
C | A | 6 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(3): Show | 7 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-1605C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82385198 | ||||||
| chr12:82385384
|
C | G | 4 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090others(1): Show | 4 | HG01884.hp2 HG02109.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-1419C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82385384 | ||||||
| chr12:82385579
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-1224A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82385579 | ||||||
| chr12:82385689
|
A | C | 1 | a0001c0001t0001g0065 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.260-1114A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82385689 | ||||||
| chr12:82385830
|
G | A | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-973G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82385830 | ||||||
| chr12:82385966
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.260-837A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82385966 | ||||||
| chr12:82386003
|
A | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.260-800A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386003 | ||||||
| chr12:82386058
|
G | T | 57 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 57 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.260-745G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386058 | ||||||
| chr12:82386077
|
C | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.260-726C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386077 | ||||||
| chr12:82386292
|
C | T | 10 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(7): Show | 11 | HG01884.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-511C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386292 | ||||||
| chr12:82386414
|
C | A | 1 | a0003c0003t0002g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.260-389C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386414 | ||||||
| chr12:82386429
|
TCCTC | T | 6 | a0002c0002t0002g0087a0002c0002t0002g0088a0002c0002t0002g0089others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.260-349_260-346del others(4): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82386429 | |||||
| chr12:82386429
|
TCCTCCCT others(5): Show |
T | 1 | a0003c0003t0002g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.260-357_260-346del others(12): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82386429 | |||||
| chr12:82386446
|
C | T | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-357C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386446 | ||||||
| chr12:82386450
|
C | T | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-353C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386450 | ||||||
| chr12:82386454
|
C | T | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.260-349C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386454 | ||||||
| chr12:82386457
|
C | T | 11 | a0001c0001t0001g0055a0003c0003t0001g0107a0003c0003t0001g0108others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-346C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386457 | ||||||
| chr12:82386458
|
T | C | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-345T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386458 | ||||||
| chr12:82386462
|
T | C | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-341T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386462 | ||||||
| chr12:82386469
|
T | C | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-334T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386469 | ||||||
| chr12:82386471
|
C | T | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-332C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386471 | ||||||
| chr12:82386473
|
C | T | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-330C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386473 | ||||||
| chr12:82386477
|
C | T | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-326C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386477 | ||||||
| chr12:82386483
|
T | C | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-320T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386483 | ||||||
| chr12:82386485
|
T | C | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-318T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386485 | ||||||
| chr12:82386488
|
T | A | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-315T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386488 | ||||||
| chr12:82386488
|
T | TTCCTCCC others(5): Show |
115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 119 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.260-304_260-303ins others(12): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 82386488 | |||||
| chr12:82386533
|
T | G | 1 | a0003c0003t0001g0113 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.260-270T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82386533 | ||||||
| chr12:82387102
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.424+135A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82387102 | ||||||
| chr12:82387132
|
A | G | 1 | a0002c0006t0004g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.424+165A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82387132 | ||||||
| chr12:82387212
|
A | T | 1 | a0001c0001t0001g0011 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.424+245A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82387212 | ||||||
| chr12:82387250
|
C | A | 7 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+283C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82387250 | ||||||
| chr12:82387485
|
A | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+518A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82387485 | ||||||
| chr12:82387713
|
G | A | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.424+746G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82387713 | ||||||
| chr12:82387715
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.424+748G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82387715 | ||||||
| chr12:82387715
|
G | GCACA | 80 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(77): Show | 82 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.424+762_424+765dup others(4): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 82387715 | |||||
| chr12:82387715
|
G | GCACACA | 8 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0118others(5): Show | 9 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+760_424+765dup others(6): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 82387715 | |||||
| chr12:82387715
|
G | GCGCA | 10 | a0001c0001t0001g0023a0003c0003t0001g0107a0003c0003t0001g0108others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+749_424+750ins others(4): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 82387715 | |||||
| chr12:82387715
|
G | GCGCACA | 2 | a0001c0001t0001g0054a0003c0003t0001g0109 | 2 | HG02970.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.424+749_424+750ins others(6): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 82387715 | |||||
| chr12:82387717
|
A | G | 1 | a0003c0003t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.424+750A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82387717 | ||||||
| chr12:82387792
|
C | T | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.424+825C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82387792 | ||||||
| chr12:82387836
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.424+869C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82387836 | ||||||
| chr12:82387946
|
A | AT | 7 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+988dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 82387946 | |||||
| chr12:82388292
|
C | A | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.424+1325C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82388292 | ||||||
| chr12:82388297
|
C | A | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+1330C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82388297 | ||||||
| chr12:82388653
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.425-1163A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82388653 | ||||||
| chr12:82389166
|
C | T | 1 | a0002c0002t0002g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.425-650C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82389166 | ||||||
| chr12:82389274
|
G | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.425-542G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82389274 | ||||||
| chr12:82389281
|
G | GA | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.425-533dupA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 82389281 | |||||
| chr12:82389371
|
G | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.425-445G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82389371 | ||||||
| chr12:82389608
|
T | C | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.425-208T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82389608 | ||||||
| chr12:82389684
|
G | C | 1 | a0001c0001t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.425-132G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 2/11 | chr12 | 82389684 | ||||||
| chr12:82390572
|
G | C | 1 | a0001c0001t0001g0010 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.531+650G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82390572 | ||||||
| chr12:82391104
|
A | G | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.531+1182A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82391104 | ||||||
| chr12:82391187
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.531+1265C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82391187 | ||||||
| chr12:82391316
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.531+1394A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82391316 | ||||||
| chr12:82391518
|
C | A | 1 | a0001c0001t0001g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.531+1596C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82391518 | ||||||
| chr12:82391540
|
A | ATGTG | 102 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.531+1632_531+1635d others(6): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 82391540 | |||||
| chr12:82391540
|
A | ATGTGTG | 23 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(20): Show | 24 | HG00738.hp2 HG01256.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.531+1630_531+1635d others(8): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 82391540 | |||||
| chr12:82391653
|
G | A | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.531+1731G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82391653 | ||||||
| chr12:82391724
|
CT | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.531+1818delT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 82391724 | |||||
| chr12:82391726
|
T | A | 7 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.531+1804T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82391726 | ||||||
| chr12:82391953
|
A | C | 3 | a0002c0006t0002g0100a0002c0006t0002g0102a0002c0006t0002g0103 | 3 | HG01256.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.531+2031A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82391953 | ||||||
| chr12:82391990
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.531+2068G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82391990 | ||||||
| chr12:82392069
|
A | AT | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.531+2154dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 82392069 | |||||
| chr12:82392081
|
T | C | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.531+2159T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82392081 | ||||||
| chr12:82392149
|
G | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.531+2227G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82392149 | ||||||
| chr12:82392194
|
C | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.531+2272C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82392194 | ||||||
| chr12:82392239
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.531+2317A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82392239 | ||||||
| chr12:82392254
|
C | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.531+2332C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82392254 | ||||||
| chr12:82392268
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.531+2346A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82392268 | ||||||
| chr12:82392374
|
T | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.531+2452T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82392374 | ||||||
| chr12:82392538
|
C | T | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.531+2616C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82392538 | ||||||
| chr12:82393248
|
C | T | 1 | a0002c0006t0002g0101 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.531+3326C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82393248 | ||||||
| chr12:82393366
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.531+3444A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82393366 | ||||||
| chr12:82393526
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 6 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.531+3604G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82393526 | ||||||
| chr12:82393544
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.531+3622A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82393544 | ||||||
| chr12:82393650
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.531+3728T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82393650 | ||||||
| chr12:82393651
|
A | T | 1 | a0008c0010t0001g0075 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.531+3729A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82393651 | ||||||
| chr12:82393677
|
TG | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.531+3758delG | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 82393677 | |||||
| chr12:82393780
|
A | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.531+3858A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82393780 | ||||||
| chr12:82393890
|
A | C | 8 | a0002c0002t0002g0106a0004c0004t0002g0093a0004c0004t0002g0094others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.531+3968A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82393890 | ||||||
| chr12:82393950
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.531+4028A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82393950 | ||||||
| chr12:82394015
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+4093C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82394015 | ||||||
| chr12:82394292
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.531+4370A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82394292 | ||||||
| chr12:82394319
|
A | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.531+4397A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82394319 | ||||||
| chr12:82394416
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.532-4379A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82394416 | ||||||
| chr12:82394452
|
C | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.532-4343C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82394452 | ||||||
| chr12:82394530
|
T | C | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.532-4265T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82394530 | ||||||
| chr12:82395423
|
G | C | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.532-3372G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82395423 | ||||||
| chr12:82395601
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.532-3194A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82395601 | ||||||
| chr12:82395637
|
G | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.532-3158G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82395637 | ||||||
| chr12:82395844
|
T | G | 8 | a0002c0002t0002g0106a0004c0004t0002g0093a0004c0004t0002g0094others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.532-2951T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82395844 | ||||||
| chr12:82396160
|
G | A | 1 | a0002c0006t0002g0100 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.532-2635G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82396160 | ||||||
| chr12:82396177
|
T | G | 1 | a0002c0002t0002g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.532-2618T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82396177 | ||||||
| chr12:82396664
|
C | A | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.532-2131C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82396664 | ||||||
| chr12:82396693
|
T | G | 3 | a0003c0003t0001g0108a0003c0003t0001g0111a0003c0003t0002g0112 | 3 | HG00738.hp2 HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.532-2102T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82396693 | ||||||
| chr12:82396873
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.532-1922C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82396873 | ||||||
| chr12:82397088
|
A | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.532-1707A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82397088 | ||||||
| chr12:82397188
|
A | G | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.532-1607A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82397188 | ||||||
| chr12:82397204
|
G | A | 6 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(3): Show | 7 | HG02451.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.532-1591G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82397204 | ||||||
| chr12:82397219
|
G | C | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.532-1576G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82397219 | ||||||
| chr12:82397291
|
A | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.532-1504A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82397291 | ||||||
| chr12:82397293
|
A | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.532-1502A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82397293 | ||||||
| chr12:82397356
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.532-1439A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82397356 | ||||||
| chr12:82397556
|
A | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.532-1239A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82397556 | ||||||
| chr12:82397718
|
T | A | 5 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(2): Show | 6 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.532-1077T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82397718 | ||||||
| chr12:82397772
|
T | C | 23 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(20): Show | 24 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.532-1023T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82397772 | ||||||
| chr12:82397964
|
C | T | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | HG00280.hp1 HG01433.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.532-831C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82397964 | ||||||
| chr12:82397974
|
T | A | 1 | a0001c0001t0001g0022 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.532-821T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82397974 | ||||||
| chr12:82398135
|
G | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.532-660G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82398135 | ||||||
| chr12:82398253
|
C | A | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.532-542C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82398253 | ||||||
| chr12:82398253
|
C | CT | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.532-531dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 82398253 | |||||
| chr12:82398253
|
CT | C | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.532-531delT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 82398253 | |||||
| chr12:82398341
|
T | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.532-454T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82398341 | ||||||
| chr12:82398359
|
G | A | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.532-436G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82398359 | ||||||
| chr12:82398406
|
A | G | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.532-389A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82398406 | ||||||
| chr12:82399577
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1131+183A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82399577 | ||||||
| chr12:82399601
|
A | G | 1 | a0002c0002t0002g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1131+207A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82399601 | ||||||
| chr12:82399754
|
A | G | 1 | a0004c0004t0002g0099 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1131+360A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82399754 | ||||||
| chr12:82399809
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1131+415T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82399809 | ||||||
| chr12:82399895
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1131+501G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82399895 | ||||||
| chr12:82399915
|
A | AT | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1131+523dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 82399915 | |||||
| chr12:82399948
|
C | CA | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 83 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1131+568dupA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 82399948 | |||||
| chr12:82399948
|
CA | C | 23 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(20): Show | 24 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.1131+568delA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 82399948 | |||||
| chr12:82400143
|
G | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1131+749G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82400143 | ||||||
| chr12:82400175
|
A | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1131+781A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82400175 | ||||||
| chr12:82400334
|
C | G | 4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(1): Show | 4 | HG02280.hp2 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1131+940C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82400334 | ||||||
| chr12:82400338
|
CAAAAAAA others(1): Show |
C | 19 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0014others(16): Show | 19 | HG00099.hp1 HG00673.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1131+948_1131+955d others(10): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 82400338 | |||||
| chr12:82400343
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1131+949A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82400343 | ||||||
| chr12:82400347
|
AAAG | A | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1131+956_1131+958d others(5): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 82400347 | |||||
| chr12:82400354
|
A | G | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1131+960A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82400354 | ||||||
| chr12:82400358
|
G | A | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1131+964G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82400358 | ||||||
| chr12:82400589
|
T | TAAAA | 69 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(66): Show | 73 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.1131+1198_1131+119 others(8): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 82400589 | |||||
| chr12:82400589
|
T | TAAAAA | 56 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1131+1198_1131+119 others(9): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 82400589 | |||||
| chr12:82400593
|
T | A | 1 | a0001c0001t0001g0067 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1131+1199T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82400593 | ||||||
| chr12:82400594
|
G | T | 1 | a0001c0001t0001g0067 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1131+1200G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82400594 | ||||||
| chr12:82400788
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1131+1394G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82400788 | ||||||
| chr12:82400791
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1131+1397A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82400791 | ||||||
| chr12:82400812
|
A | G | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1131+1418A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82400812 | ||||||
| chr12:82401088
|
A | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1131+1694A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82401088 | ||||||
| chr12:82401094
|
A | G | 7 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1131+1700A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82401094 | ||||||
| chr12:82401575
|
G | A | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1132-1408G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82401575 | ||||||
| chr12:82401768
|
A | C | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1132-1215A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82401768 | ||||||
| chr12:82402008
|
G | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1132-975G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82402008 | ||||||
| chr12:82402041
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1132-942A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82402041 | ||||||
| chr12:82402124
|
G | A | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1132-859G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82402124 | ||||||
| chr12:82402147
|
A | G | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1132-836A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82402147 | ||||||
| chr12:82402227
|
G | A | 4 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090others(1): Show | 4 | HG01884.hp2 HG02109.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1132-756G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82402227 | ||||||
| chr12:82402232
|
A | G | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1132-751A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82402232 | ||||||
| chr12:82402255
|
A | AAGTAG | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1132-726_1132-722d others(7): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 82402255 | |||||
| chr12:82402323
|
C | A | 1 | a0005c0007t0001g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1132-660C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82402323 | ||||||
| chr12:82402552
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1132-431G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82402552 | ||||||
| chr12:82402599
|
T | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1132-384T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82402599 | ||||||
| chr12:82402625
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1132-358T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82402625 | ||||||
| chr12:82402784
|
A | T | 1 | a0001c0001t0001g0032 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1132-199A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82402784 | ||||||
| chr12:82402809
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1132-174G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82402809 | ||||||
| chr12:82402845
|
G | A | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1132-138G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82402845 | ||||||
| chr12:82403307
|
A | G | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1279+177A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82403307 | ||||||
| chr12:82403402
|
A | G | 1 | a0002c0002t0002g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1279+272A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82403402 | ||||||
| chr12:82403498
|
T | C | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+368T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82403498 | ||||||
| chr12:82403822
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1279+692C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82403822 | ||||||
| chr12:82404332
|
A | T | 1 | a0003c0003t0001g0109 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1279+1202A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82404332 | ||||||
| chr12:82404345
|
A | G | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+1215A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82404345 | ||||||
| chr12:82404465
|
G | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1279+1335G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82404465 | ||||||
| chr12:82404483
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+1353C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82404483 | ||||||
| chr12:82404509
|
T | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0070 | 2 | HG01978.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1279+1379T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82404509 | ||||||
| chr12:82404570
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+1440A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82404570 | ||||||
| chr12:82404621
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1279+1491A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82404621 | ||||||
| chr12:82404790
|
A | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062 | 3 | HG02280.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1279+1660A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82404790 | ||||||
| chr12:82404848
|
G | A | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1279+1718G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82404848 | ||||||
| chr12:82404869
|
A | T | 1 | a0001c0001t0001g0078 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1279+1739A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82404869 | ||||||
| chr12:82404949
|
GA | G | 89 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 91 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1279+1833delA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82404949 | |||||
| chr12:82405033
|
T | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1279+1903T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82405033 | ||||||
| chr12:82405197
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1279+2067C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82405197 | ||||||
| chr12:82405344
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1279+2214C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82405344 | ||||||
| chr12:82405494
|
A | G | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+2364A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82405494 | ||||||
| chr12:82405724
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1279+2594G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82405724 | ||||||
| chr12:82405818
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1279+2688A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82405818 | ||||||
| chr12:82405970
|
G | A | 4 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090others(1): Show | 4 | HG01884.hp2 HG02109.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1279+2840G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82405970 | ||||||
| chr12:82406397
|
C | A | 1 | a0002c0002t0002g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1279+3267C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82406397 | ||||||
| chr12:82406415
|
T | C | 1 | a0002c0002t0002g0089 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1279+3285T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82406415 | ||||||
| chr12:82406418
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0039others(2): Show | 5 | HG00673.hp2 HG02523.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+3288G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82406418 | ||||||
| chr12:82406719
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1279+3589A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82406719 | ||||||
| chr12:82406749
|
C | T | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1279+3619C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82406749 | ||||||
| chr12:82406932
|
T | G | 1 | a0001c0001t0001g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1279+3802T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82406932 | ||||||
| chr12:82407068
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1279+3938C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82407068 | ||||||
| chr12:82407289
|
C | G | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1279+4159C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82407289 | ||||||
| chr12:82407289
|
C | T | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+4159C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82407289 | ||||||
| chr12:82407307
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1279+4177G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82407307 | ||||||
| chr12:82407345
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1279+4215A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82407345 | ||||||
| chr12:82407517
|
C | G | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1279+4387C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82407517 | ||||||
| chr12:82407547
|
A | G | 1 | a0004c0004t0002g0098 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1279+4417A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82407547 | ||||||
| chr12:82408014
|
G | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+4884G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82408014 | ||||||
| chr12:82408085
|
G | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0063 | 3 | HG02886.hp1 HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1279+4955G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82408085 | ||||||
| chr12:82408232
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1279+5102G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82408232 | ||||||
| chr12:82408280
|
A | T | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1279+5150A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82408280 | ||||||
| chr12:82408287
|
G | A | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1279+5157G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82408287 | ||||||
| chr12:82408335
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1279+5205A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82408335 | ||||||
| chr12:82408597
|
C | CGTGT | 10 | a0001c0001t0001g0057a0003c0003t0001g0107a0003c0003t0001g0108others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1279+5493_1279+549 others(8): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82408597 | |||||
| chr12:82408597
|
C | CGTGTGT | 64 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1279+5491_1279+549 others(10): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82408597 | |||||
| chr12:82408597
|
C | CGTGTGTG others(1): Show |
21 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0036others(18): Show | 24 | HG01884.hp1 HG01978.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1279+5489_1279+549 others(12): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82408597 | |||||
| chr12:82408597
|
C | CGTGTGTG others(3): Show |
20 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(17): Show | 21 | HG01256.hp2 HG01516.hp1 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.1279+5487_1279+549 others(14): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82408597 | |||||
| chr12:82408597
|
C | CGTGTGTG others(5): Show |
5 | a0001c0005t0001g0069a0002c0002t0002g0086a0002c0002t0002g0092others(2): Show | 5 | HG01361.hp1 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+5485_1279+549 others(16): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82408597 | |||||
| chr12:82408597
|
C | CGTGTGTG others(9): Show |
3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1279+5481_1279+549 others(20): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82408597 | |||||
| chr12:82409006
|
A | C | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 83 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1279+5876A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82409006 | ||||||
| chr12:82409087
|
A | G | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1279+5957A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82409087 | ||||||
| chr12:82409294
|
G | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1279+6164G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82409294 | ||||||
| chr12:82409404
|
A | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1279+6274A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82409404 | ||||||
| chr12:82409428
|
G | A | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+6298G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82409428 | ||||||
| chr12:82409554
|
C | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 83 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1279+6424C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82409554 | ||||||
| chr12:82409695
|
A | G | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1279+6565A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82409695 | ||||||
| chr12:82410148
|
GCTTA | G | 7 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1279+7023_1279+702 others(8): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82410148 | |||||
| chr12:82410182
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1279+7052C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82410182 | ||||||
| chr12:82410189
|
T | C | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1279+7059T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82410189 | ||||||
| chr12:82410323
|
A | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1279+7193A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82410323 | ||||||
| chr12:82410333
|
C | T | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1279+7203C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82410333 | ||||||
| chr12:82410416
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1279+7286A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82410416 | ||||||
| chr12:82410615
|
T | G | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+7485T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82410615 | ||||||
| chr12:82410724
|
A | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1279+7594A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82410724 | ||||||
| chr12:82410815
|
C | T | 6 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(3): Show | 7 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+7685C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82410815 | ||||||
| chr12:82411051
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1279+7921T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82411051 | ||||||
| chr12:82411200
|
AC | A | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+8071delC | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82411200 | ||||||
| chr12:82411488
|
A | G | 3 | a0003c0003t0001g0108a0003c0003t0001g0111a0003c0003t0002g0112 | 3 | HG00738.hp2 HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1279+8358A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82411488 | ||||||
| chr12:82411603
|
A | G | 1 | a0004c0004t0002g0097 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1279+8473A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82411603 | ||||||
| chr12:82411853
|
C | T | 6 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(3): Show | 7 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+8723C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82411853 | ||||||
| chr12:82412175
|
CA | C | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1279+9053delA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82412175 | |||||
| chr12:82412259
|
T | C | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+9129T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82412259 | ||||||
| chr12:82412744
|
A | T | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1279+9614A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82412744 | ||||||
| chr12:82412756
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+9626A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82412756 | ||||||
| chr12:82412937
|
C | T | 1 | a0002c0006t0002g0101 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1279+9807C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82412937 | ||||||
| chr12:82412975
|
T | A | 1 | a0001c0001t0001g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1279+9845T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82412975 | ||||||
| chr12:82413097
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1279+9967G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82413097 | ||||||
| chr12:82413711
|
G | A | 14 | a0002c0002t0002g0106a0002c0006t0002g0100a0002c0006t0002g0101others(11): Show | 14 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.1279+10581G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82413711 | ||||||
| chr12:82413998
|
A | T | 1 | a0002c0006t0002g0100 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1279+10868A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82413998 | ||||||
| chr12:82414362
|
A | G | 2 | a0005c0007t0001g0046a0005c0007t0001g0047 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1279+11232A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82414362 | ||||||
| chr12:82414437
|
A | G | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1279+11307A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82414437 | ||||||
| chr12:82414530
|
C | G | 1 | a0002c0002t0002g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1279+11400C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82414530 | ||||||
| chr12:82414660
|
A | G | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+11530A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82414660 | ||||||
| chr12:82414697
|
G | A | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1279+11567G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82414697 | ||||||
| chr12:82414757
|
CATTTT | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1279+11630_1279+11 others(11): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82414757 | |||||
| chr12:82414828
|
G | A | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1279+11698G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82414828 | ||||||
| chr12:82414860
|
T | C | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+11730T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82414860 | ||||||
| chr12:82414993
|
C | T | 14 | a0002c0002t0002g0106a0002c0006t0002g0100a0002c0006t0002g0101others(11): Show | 14 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.1279+11863C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82414993 | ||||||
| chr12:82415131
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1279+12001C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82415131 | ||||||
| chr12:82415190
|
A | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1279+12060A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82415190 | ||||||
| chr12:82415209
|
A | G | 8 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1279+12079A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82415209 | ||||||
| chr12:82415417
|
G | A | 1 | a0006c0012t0001g0045 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1279+12287G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82415417 | ||||||
| chr12:82415478
|
C | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1279+12348C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82415478 | ||||||
| chr12:82415563
|
G | T | 5 | a0003c0003t0001g0108a0003c0003t0001g0109a0003c0003t0001g0110others(2): Show | 5 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+12433G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82415563 | ||||||
| chr12:82415624
|
T | C | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1279+12494T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82415624 | ||||||
| chr12:82415642
|
C | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1279+12512C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82415642 | ||||||
| chr12:82415738
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+12608C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82415738 | ||||||
| chr12:82415853
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+12723C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82415853 | ||||||
| chr12:82415987
|
C | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0070 | 2 | HG01978.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1279+12857C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82415987 | ||||||
| chr12:82415992
|
C | T | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1279+12862C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82415992 | ||||||
| chr12:82416099
|
T | C | 14 | a0002c0002t0002g0106a0002c0006t0002g0100a0002c0006t0002g0101others(11): Show | 14 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.1279+12969T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82416099 | ||||||
| chr12:82416152
|
G | A | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1279+13022G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82416152 | ||||||
| chr12:82416446
|
G | GT | 82 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(79): Show | 84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1279+13331dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82416446 | |||||
| chr12:82416467
|
A | G | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1279+13337A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82416467 | ||||||
| chr12:82416584
|
G | C | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1279+13454G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82416584 | ||||||
| chr12:82416616
|
T | TTTTTG | 6 | a0001c0001t0001g0030a0001c0001t0001g0049a0001c0001t0001g0050others(3): Show | 6 | HG00280.hp1 HG01433.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279+13511_1279+13 others(11): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82416616 | |||||
| chr12:82416620
|
T | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0053 | 2 | HG03834.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1279+13490T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82416620 | ||||||
| chr12:82416651
|
T | G | 1 | a0001c0001t0001g0004 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1279+13521T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82416651 | ||||||
| chr12:82416710
|
C | T | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+13580C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82416710 | ||||||
| chr12:82416867
|
C | T | 2 | a0001c0001t0001g0051a0002c0002t0002g0106 | 2 | HG02630.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1279+13737C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82416867 | ||||||
| chr12:82416875
|
A | G | 8 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1279+13745A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82416875 | ||||||
| chr12:82416920
|
T | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0032others(1): Show | 4 | HG00280.hp2 HG01358.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1279+13790T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82416920 | ||||||
| chr12:82416957
|
C | G | 1 | a0005c0007t0001g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1279+13827C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82416957 | ||||||
| chr12:82417133
|
G | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1280-13760G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82417133 | ||||||
| chr12:82417412
|
C | T | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1280-13481C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82417412 | ||||||
| chr12:82417845
|
AGATGACG others(6): Show |
A | 1 | a0003c0003t0001g0116 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1280-13047_1280-13 others(19): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82417845 | ||||||
| chr12:82417854
|
T | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062 | 3 | HG02280.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1280-13039T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82417854 | ||||||
| chr12:82417876
|
G | A | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1280-13017G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82417876 | ||||||
| chr12:82418063
|
A | G | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1280-12830A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82418063 | ||||||
| chr12:82418282
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1280-12611A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82418282 | ||||||
| chr12:82418368
|
G | C | 1 | a0003c0003t0002g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1280-12525G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82418368 | ||||||
| chr12:82418391
|
A | T | 8 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1280-12502A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82418391 | ||||||
| chr12:82418608
|
T | C | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1280-12285T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82418608 | ||||||
| chr12:82418788
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1280-12105G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82418788 | ||||||
| chr12:82418953
|
A | C | 3 | a0002c0006t0002g0100a0002c0006t0002g0102a0002c0006t0002g0103 | 3 | HG01256.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1280-11940A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82418953 | ||||||
| chr12:82418972
|
T | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1280-11921T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82418972 | ||||||
| chr12:82419093
|
A | G | 8 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1280-11800A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82419093 | ||||||
| chr12:82419376
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1280-11517G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82419376 | ||||||
| chr12:82419671
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1280-11222T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82419671 | ||||||
| chr12:82419672
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1280-11221A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82419672 | ||||||
| chr12:82419682
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1280-11211A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82419682 | ||||||
| chr12:82419693
|
T | TAA | 6 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0041others(3): Show | 6 | HG01516.hp2 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280-11190_1280-11 others(8): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82419693 | |||||
| chr12:82419693
|
T | TAAA | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(90): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1280-11191_1280-11 others(9): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82419693 | |||||
| chr12:82419746
|
CT | C | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1280-11143delT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82419746 | |||||
| chr12:82419760
|
G | A | 8 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1280-11133G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82419760 | ||||||
| chr12:82420064
|
A | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1280-10829A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82420064 | ||||||
| chr12:82420152
|
A | G | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-10741A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82420152 | ||||||
| chr12:82420301
|
T | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0067 | 2 | NA18959.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1280-10592T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82420301 | ||||||
| chr12:82420371
|
G | T | 1 | a0002c0002t0002g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1280-10522G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82420371 | ||||||
| chr12:82420437
|
C | T | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1280-10456C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82420437 | ||||||
| chr12:82420472
|
G | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | HG00099.hp1 HG01433.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1280-10421G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82420472 | ||||||
| chr12:82420702
|
G | A | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1280-10191G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82420702 | ||||||
| chr12:82420755
|
T | G | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-10138T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82420755 | ||||||
| chr12:82420853
|
A | AT | 8 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0084others(5): Show | 9 | HG01884.hp1 HG02273.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.1280-10029dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82420853 | |||||
| chr12:82420853
|
AT | A | 6 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(3): Show | 7 | HG02451.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1280-10029delT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82420853 | |||||
| chr12:82420863
|
T | C | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1280-10030T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82420863 | ||||||
| chr12:82420865
|
C | G | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1280-10028C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82420865 | ||||||
| chr12:82420900
|
G | C | 1 | a0002c0002t0002g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1280-9993G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82420900 | ||||||
| chr12:82420925
|
G | A | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280-9968G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82420925 | ||||||
| chr12:82421051
|
G | A | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1280-9842G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82421051 | ||||||
| chr12:82421208
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1280-9685G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82421208 | ||||||
| chr12:82421518
|
A | C | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1280-9375A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82421518 | ||||||
| chr12:82421581
|
T | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1280-9312T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82421581 | ||||||
| chr12:82421600
|
C | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1280-9293C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82421600 | ||||||
| chr12:82421784
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1280-9109C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82421784 | ||||||
| chr12:82422136
|
C | A | 1 | a0001c0001t0001g0033 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1280-8757C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82422136 | ||||||
| chr12:82422184
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1280-8709A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82422184 | ||||||
| chr12:82422332
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1280-8561C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82422332 | ||||||
| chr12:82422349
|
C | G | 1 | a0001c0001t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1280-8544C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82422349 | ||||||
| chr12:82422414
|
G | T | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1280-8479G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82422414 | ||||||
| chr12:82422582
|
A | G | 1 | a0006c0012t0001g0045 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1280-8311A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82422582 | ||||||
| chr12:82422595
|
G | A | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1280-8298G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82422595 | ||||||
| chr12:82422809
|
G | C | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1280-8084G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82422809 | ||||||
| chr12:82422809
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1280-8084G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82422809 | ||||||
| chr12:82422911
|
G | C | 1 | a0001c0001t0001g0083 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1280-7982G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82422911 | ||||||
| chr12:82422952
|
G | A | 1 | a0003c0003t0002g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1280-7941G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82422952 | ||||||
| chr12:82422992
|
T | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1280-7901T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82422992 | ||||||
| chr12:82423065
|
A | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1280-7828A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82423065 | ||||||
| chr12:82423068
|
A | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1280-7825A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82423068 | ||||||
| chr12:82423070
|
G | T | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1280-7823G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82423070 | ||||||
| chr12:82423157
|
A | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1280-7736A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82423157 | ||||||
| chr12:82423385
|
A | G | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1280-7508A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82423385 | ||||||
| chr12:82423410
|
T | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 6 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280-7483T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82423410 | ||||||
| chr12:82423449
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1280-7444A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82423449 | ||||||
| chr12:82423492
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1280-7401T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82423492 | ||||||
| chr12:82423495
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1280-7398G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82423495 | ||||||
| chr12:82423496
|
A | T | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280-7397A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82423496 | ||||||
| chr12:82423499
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1280-7394A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82423499 | ||||||
| chr12:82423592
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1280-7301G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82423592 | ||||||
| chr12:82423631
|
G | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1280-7262G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82423631 | ||||||
| chr12:82423864
|
A | G | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1280-7029A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82423864 | ||||||
| chr12:82423935
|
C | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1280-6958C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82423935 | ||||||
| chr12:82424076
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1280-6817C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82424076 | ||||||
| chr12:82424279
|
C | G | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1280-6614C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82424279 | ||||||
| chr12:82424280
|
G | A | 1 | a0001c0005t0001g0012 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1280-6613G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82424280 | ||||||
| chr12:82424335
|
T | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1280-6558T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82424335 | ||||||
| chr12:82424363
|
G | A | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-6530G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82424363 | ||||||
| chr12:82424542
|
C | CTA | 2 | a0003c0003t0001g0107a0003c0003t0001g0114 | 2 | HG01891.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1280-6335_1280-633 others(6): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82424542 | |||||
| chr12:82424542
|
CTA | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 98 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1280-6335_1280-633 others(6): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82424542 | |||||
| chr12:82424542
|
CTATATAT others(1): Show |
C | 10 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(7): Show | 11 | HG01884.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-6341_1280-633 others(12): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82424542 | |||||
| chr12:82424547
|
T | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0080 | 2 | HG01361.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1280-6346T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82424547 | ||||||
| chr12:82424549
|
T | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0080 | 2 | HG01361.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1280-6344T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82424549 | ||||||
| chr12:82424625
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1280-6268T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82424625 | ||||||
| chr12:82424855
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1280-6038G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82424855 | ||||||
| chr12:82424892
|
T | C | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280-6001T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82424892 | ||||||
| chr12:82425065
|
G | T | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1280-5828G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82425065 | ||||||
| chr12:82425185
|
C | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1280-5708C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82425185 | ||||||
| chr12:82425349
|
C | G | 1 | a0003c0003t0001g0109 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1280-5544C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82425349 | ||||||
| chr12:82425359
|
A | G | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1280-5534A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82425359 | ||||||
| chr12:82425421
|
G | A | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1280-5472G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82425421 | ||||||
| chr12:82425532
|
C | T | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1280-5361C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82425532 | ||||||
| chr12:82425642
|
A | G | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1280-5251A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82425642 | ||||||
| chr12:82425650
|
C | G | 1 | a0001c0001t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1280-5243C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82425650 | ||||||
| chr12:82426064
|
C | T | 1 | a0002c0006t0004g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1280-4829C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82426064 | ||||||
| chr12:82426351
|
C | T | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1280-4542C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82426351 | ||||||
| chr12:82426377
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1280-4516T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82426377 | ||||||
| chr12:82427218
|
A | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0032others(1): Show | 4 | HG00280.hp2 HG01358.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1280-3675A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82427218 | ||||||
| chr12:82427326
|
G | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1280-3567G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82427326 | ||||||
| chr12:82427805
|
AT | A | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1280-3084delT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82427805 | |||||
| chr12:82427881
|
A | G | 18 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(15): Show | 19 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1280-3012A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82427881 | ||||||
| chr12:82427998
|
G | A | 4 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090others(1): Show | 4 | HG01884.hp2 HG02109.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1280-2895G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82427998 | ||||||
| chr12:82428101
|
A | T | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1280-2792A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82428101 | ||||||
| chr12:82428188
|
C | T | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-2705C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82428188 | ||||||
| chr12:82428216
|
C | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1280-2677C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82428216 | ||||||
| chr12:82428385
|
CT | C | 8 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1280-2507delT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82428385 | ||||||
| chr12:82428414
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1280-2479C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82428414 | ||||||
| chr12:82428630
|
G | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1280-2263G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82428630 | ||||||
| chr12:82428631
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1280-2262A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82428631 | ||||||
| chr12:82428776
|
GT | G | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1280-2114delT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82428776 | |||||
| chr12:82429145
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1280-1748A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82429145 | ||||||
| chr12:82429357
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0048a0001c0001t0001g0053others(2): Show | 5 | HG00673.hp1 HG01952.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280-1536A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82429357 | ||||||
| chr12:82429376
|
G | GT | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280-1502dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82429376 | |||||
| chr12:82429376
|
GT | G | 23 | a0001c0001t0001g0023a0002c0002t0002g0092a0002c0002t0002g0106others(20): Show | 23 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.1280-1502delT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82429376 | |||||
| chr12:82429376
|
GTT | G | 91 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1280-1503_1280-150 others(6): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82429376 | |||||
| chr12:82429636
|
T | G | 1 | a0002c0002t0002g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1280-1257T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82429636 | ||||||
| chr12:82430198
|
A | T | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1280-695A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82430198 | ||||||
| chr12:82430326
|
C | CAT | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1280-566_1280-565i others(4): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 82430326 | |||||
| chr12:82431008
|
G | A | 8 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1374+21G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82431008 | ||||||
| chr12:82431112
|
T | G | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1374+125T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82431112 | ||||||
| chr12:82431242
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1374+255G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82431242 | ||||||
| chr12:82431413
|
T | G | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1374+426T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82431413 | ||||||
| chr12:82431488
|
A | T | 1 | a0001c0001t0001g0022 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1374+501A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82431488 | ||||||
| chr12:82431747
|
C | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1374+760C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82431747 | ||||||
| chr12:82431916
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1374+929T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82431916 | ||||||
| chr12:82432317
|
T | G | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1374+1330T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82432317 | ||||||
| chr12:82432430
|
C | T | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1374+1443C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82432430 | ||||||
| chr12:82432495
|
A | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1374+1508A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82432495 | ||||||
| chr12:82432497
|
C | A | 1 | a0002c0002t0002g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1374+1510C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82432497 | ||||||
| chr12:82432602
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1374+1615A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82432602 | ||||||
| chr12:82432811
|
C | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1374+1824C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82432811 | ||||||
| chr12:82432863
|
TA | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 86 | HG00099.hp1 HG00673.hp1 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.1375-1812delA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 82432863 | |||||
| chr12:82432863
|
TAA | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0037others(18): Show | 22 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1375-1813_1375-181 others(6): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 82432863 | |||||
| chr12:82433008
|
A | C | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1375-1687A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82433008 | ||||||
| chr12:82433217
|
T | G | 1 | a0001c0001t0001g0032 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1375-1478T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82433217 | ||||||
| chr12:82433343
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1375-1352T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82433343 | ||||||
| chr12:82433447
|
A | T | 18 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(15): Show | 19 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1375-1248A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82433447 | ||||||
| chr12:82433787
|
T | C | 1 | a0003c0003t0001g0115 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1375-908T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82433787 | ||||||
| chr12:82433950
|
C | T | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1375-745C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82433950 | ||||||
| chr12:82434121
|
A | G | 1 | a0003c0003t0001g0107 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1375-574A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82434121 | ||||||
| chr12:82434156
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1375-539A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82434156 | ||||||
| chr12:82434256
|
G | T | 5 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(2): Show | 6 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1375-439G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82434256 | ||||||
| chr12:82434290
|
T | C | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1375-405T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | chr12 | 82434290 | ||||||
| chr12:82434647
|
T | TATAAG | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1375-46_1375-42dup others(5): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 82434647 | |||||
| chr12:82435045
|
C | T | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1404+321C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82435045 | ||||||
| chr12:82435139
|
T | A | 1 | a0001c0001t0001g0055 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1404+415T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82435139 | ||||||
| chr12:82435457
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1404+733T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82435457 | ||||||
| chr12:82435525
|
C | T | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1404+801C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82435525 | ||||||
| chr12:82435577
|
T | C | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1404+853T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82435577 | ||||||
| chr12:82435886
|
G | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1404+1162G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82435886 | ||||||
| chr12:82435911
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1404+1187A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82435911 | ||||||
| chr12:82435955
|
C | T | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1404+1231C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82435955 | ||||||
| chr12:82436069
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1404+1345G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82436069 | ||||||
| chr12:82436135
|
G | T | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1404+1411G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82436135 | ||||||
| chr12:82436156
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0002c0006t0002g0100 | 3 | HG01256.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1404+1432A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82436156 | ||||||
| chr12:82436168
|
G | A | 3 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086 | 4 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1404+1444G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82436168 | ||||||
| chr12:82436397
|
T | G | 1 | a0002c0002t0002g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1404+1673T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82436397 | ||||||
| chr12:82436411
|
G | A | 1 | a0003c0003t0002g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1404+1687G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82436411 | ||||||
| chr12:82436842
|
T | C | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1405-1876T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82436842 | ||||||
| chr12:82436892
|
A | G | 3 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086 | 4 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1405-1826A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82436892 | ||||||
| chr12:82436893
|
T | C | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073 | 3 | NA18959.hp2 NA19060.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1405-1825T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82436893 | ||||||
| chr12:82437015
|
T | C | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1405-1703T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82437015 | ||||||
| chr12:82437035
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1405-1683A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82437035 | ||||||
| chr12:82437593
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1405-1125T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82437593 | ||||||
| chr12:82437611
|
C | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1405-1107C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82437611 | ||||||
| chr12:82438066
|
T | C | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1405-652T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82438066 | ||||||
| chr12:82438512
|
C | CT | 5 | a0001c0001t0001g0049a0001c0001t0001g0119a0003c0003t0002g0124others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1405-191dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 82438512 | |||||
| chr12:82438512
|
C | CTT | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1405-192_1405-191d others(4): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 82438512 | |||||
| chr12:82438512
|
CT | C | 4 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1405-191delT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 82438512 | |||||
| chr12:82438639
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1405-79G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82438639 | ||||||
| chr12:82438673
|
G | GT | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1405-37dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 82438673 | |||||
| chr12:82439330
|
G | A | 11 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1478+539G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82439330 | ||||||
| chr12:82439351
|
G | T | 1 | a0001c0001t0001g0036 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1478+560G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82439351 | ||||||
| chr12:82439484
|
G | A | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1478+693G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82439484 | ||||||
| chr12:82439676
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1478+885T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82439676 | ||||||
| chr12:82439696
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1478+905A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82439696 | ||||||
| chr12:82439867
|
T | TTTA | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1478+1079_1478+108 others(7): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82439867 | |||||
| chr12:82440097
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1478+1306A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82440097 | ||||||
| chr12:82440365
|
A | G | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1478+1574A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82440365 | ||||||
| chr12:82440533
|
T | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0067 | 2 | NA18959.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1478+1742T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82440533 | ||||||
| chr12:82440664
|
G | C | 1 | a0001c0001t0001g0037 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1478+1873G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82440664 | ||||||
| chr12:82440883
|
A | C | 8 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1478+2092A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82440883 | ||||||
| chr12:82440901
|
A | G | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1478+2110A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82440901 | ||||||
| chr12:82441006
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1478+2215A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441006 | ||||||
| chr12:82441132
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1478+2341G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441132 | ||||||
| chr12:82441292
|
T | TTA | 12 | a0002c0002t0002g0126a0003c0003t0001g0107a0003c0003t0001g0108others(9): Show | 12 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1478+2516_1478+251 others(6): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82441292 | |||||
| chr12:82441292
|
T | TTATA | 80 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(77): Show | 82 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1478+2514_1478+251 others(8): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82441292 | |||||
| chr12:82441292
|
T | TTATATA | 3 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0060 | 3 | HG03225.hp1 HG03225.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1478+2512_1478+251 others(10): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82441292 | |||||
| chr12:82441361
|
C | T | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1478+2570C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441361 | ||||||
| chr12:82441409
|
G | A | 1 | a0002c0002t0002g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1478+2618G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441409 | ||||||
| chr12:82441467
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1478+2676T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441467 | ||||||
| chr12:82441489
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1478+2698G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441489 | ||||||
| chr12:82441519
|
G | A | 1 | a0002c0002t0002g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1478+2728G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441519 | ||||||
| chr12:82441613
|
C | T | 1 | a0002c0002t0002g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1478+2822C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441613 | ||||||
| chr12:82441618
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1478+2827C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441618 | ||||||
| chr12:82441768
|
A | G | 5 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(2): Show | 6 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1478+2977A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441768 | ||||||
| chr12:82441786
|
C | CA | 10 | a0001c0001t0001g0041a0004c0004t0002g0093a0004c0004t0002g0094others(7): Show | 10 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1478+3010dupA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82441786 | |||||
| chr12:82441802
|
T | A | 8 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1478+3011T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441802 | ||||||
| chr12:82441806
|
A | AACAC | 2 | a0001c0001t0001g0036a0002c0002t0002g0087 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1478+3039_1478+304 others(8): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82441806 | |||||
| chr12:82441806
|
A | AACACACA others(1): Show |
3 | a0001c0001t0001g0063a0003c0003t0002g0124a0003c0008t0001g0117 | 3 | HG02055.hp1 HG02735.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1478+3035_1478+304 others(12): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82441806 | |||||
| chr12:82441806
|
A | AACACACA others(3): Show |
54 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(51): Show | 55 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1478+3033_1478+304 others(14): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82441806 | |||||
| chr12:82441806
|
A | AACACACA others(5): Show |
22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(19): Show | 24 | HG00738.hp1 HG01257.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1478+3031_1478+304 others(16): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82441806 | |||||
| chr12:82441806
|
A | AACACACA others(7): Show |
6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG00280.hp1 HG01433.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1478+3029_1478+304 others(18): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82441806 | |||||
| chr12:82441806
|
A | AACACACA others(9): Show |
7 | a0001c0001t0001g0061a0001c0001t0001g0062a0002c0002t0002g0002others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1478+3027_1478+304 others(20): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82441806 | |||||
| chr12:82441806
|
A | AACACACA others(11): Show |
5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1478+3025_1478+304 others(22): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82441806 | |||||
| chr12:82441806
|
A | AACACACA others(3): Show |
1 | a0001c0001t0003g0031 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1478+3022_1478+302 others(14): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82441806 | |||||
| chr12:82441806
|
A | ACACACAC others(4): Show |
2 | a0001c0001t0001g0035a0001c0001t0001g0065 | 2 | HG01257.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1478+3015_1478+301 others(15): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441806 | ||||||
| chr12:82441806
|
A | ACACACAC others(6): Show |
2 | a0001c0001t0001g0016a0001c0001t0001g0022 | 2 | HG01433.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1478+3015_1478+301 others(17): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441806 | ||||||
| chr12:82441806
|
A | ACACACAC others(8): Show |
1 | a0002c0002t0002g0085 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1478+3015_1478+301 others(19): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441806 | ||||||
| chr12:82441806
|
A | ACACACAC others(10): Show |
1 | a0001c0001t0001g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1478+3015_1478+301 others(21): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441806 | ||||||
| chr12:82441806
|
A | ACACACAC others(16): Show |
1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1478+3015_1478+301 others(27): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441806 | ||||||
| chr12:82441806
|
AACAC | A | 9 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0110others(6): Show | 9 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1478+3039_1478+304 others(8): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82441806 | |||||
| chr12:82441858
|
C | T | 3 | a0005c0007t0001g0024a0005c0007t0001g0046a0005c0007t0001g0047 | 3 | HG02976.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1478+3067C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441858 | ||||||
| chr12:82442093
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1478+3302T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82442093 | ||||||
| chr12:82442197
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1478+3406A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82442197 | ||||||
| chr12:82442307
|
G | C | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1478+3516G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82442307 | ||||||
| chr12:82442465
|
A | G | 4 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090others(1): Show | 4 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1478+3674A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82442465 | ||||||
| chr12:82442509
|
A | G | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1478+3718A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82442509 | ||||||
| chr12:82442743
|
C | T | 8 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1478+3952C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82442743 | ||||||
| chr12:82442921
|
T | C | 1 | a0002c0006t0002g0102 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1478+4130T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82442921 | ||||||
| chr12:82442955
|
ATAAT | A | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1478+4169_1478+417 others(8): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82442955 | |||||
| chr12:82443025
|
G | A | 5 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(2): Show | 5 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1478+4234G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82443025 | ||||||
| chr12:82443321
|
C | A | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1478+4530C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82443321 | ||||||
| chr12:82443426
|
A | G | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1478+4635A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82443426 | ||||||
| chr12:82443462
|
CA | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1478+4688delA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82443462 | |||||
| chr12:82443819
|
AACTC | A | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1478+5036_1478+503 others(8): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82443819 | |||||
| chr12:82444086
|
A | T | 1 | a0008c0010t0001g0075 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1478+5295A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82444086 | ||||||
| chr12:82444503
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1478+5712G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82444503 | ||||||
| chr12:82444722
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1478+5931A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82444722 | ||||||
| chr12:82444771
|
A | T | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1478+5980A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82444771 | ||||||
| chr12:82444809
|
A | C | 1 | a0001c0001t0001g0030 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1478+6018A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82444809 | ||||||
| chr12:82444936
|
C | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0032others(1): Show | 4 | HG00280.hp2 HG01358.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1478+6145C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82444936 | ||||||
| chr12:82445388
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0064 | 2 | HG02523.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1478+6597T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82445388 | ||||||
| chr12:82445479
|
C | G | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1478+6688C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82445479 | ||||||
| chr12:82445668
|
G | A | 8 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1478+6877G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82445668 | ||||||
| chr12:82445863
|
T | G | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1478+7072T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82445863 | ||||||
| chr12:82445885
|
A | T | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1478+7094A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82445885 | ||||||
| chr12:82445922
|
G | A | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1478+7131G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82445922 | ||||||
| chr12:82446469
|
C | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1478+7678C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82446469 | ||||||
| chr12:82446493
|
C | T | 1 | a0001c0005t0001g0007 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1478+7702C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82446493 | ||||||
| chr12:82446508
|
CAA | C | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1478+7718_1478+771 others(6): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82446508 | ||||||
| chr12:82446564
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1478+7773A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82446564 | ||||||
| chr12:82446611
|
C | CT | 5 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0032others(2): Show | 5 | HG01358.hp2 HG01952.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.1478+7837dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82446611 | |||||
| chr12:82446611
|
CTTTTTT | C | 5 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(2): Show | 6 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1478+7832_1478+783 others(10): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82446611 | |||||
| chr12:82446685
|
C | T | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1478+7894C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82446685 | ||||||
| chr12:82446709
|
C | T | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(90): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1478+7918C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82446709 | ||||||
| chr12:82446774
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1478+7983A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82446774 | ||||||
| chr12:82446961
|
C | A | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1478+8170C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82446961 | ||||||
| chr12:82446993
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1478+8202G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82446993 | ||||||
| chr12:82447262
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1478+8471C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82447262 | ||||||
| chr12:82447622
|
C | T | 1 | a0002c0002t0002g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1478+8831C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82447622 | ||||||
| chr12:82447675
|
AGAG | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1478+8888_1478+889 others(7): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82447675 | |||||
| chr12:82447937
|
T | C | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1479-8790T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82447937 | ||||||
| chr12:82447986
|
A | G | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1479-8741A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82447986 | ||||||
| chr12:82448126
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1479-8601A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82448126 | ||||||
| chr12:82448168
|
T | A | 1 | a0001c0001t0001g0073 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1479-8559T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82448168 | ||||||
| chr12:82448374
|
T | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0070 | 2 | HG01978.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1479-8353T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82448374 | ||||||
| chr12:82448402
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1479-8325T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82448402 | ||||||
| chr12:82448508
|
C | T | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1479-8219C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82448508 | ||||||
| chr12:82448668
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1479-8059T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82448668 | ||||||
| chr12:82448819
|
A | ATGC | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1479-7906_1479-790 others(7): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82448819 | |||||
| chr12:82448819
|
A | ATGT | 17 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(14): Show | 18 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.1479-7905_1479-790 others(7): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82448819 | |||||
| chr12:82448831
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1479-7896T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82448831 | ||||||
| chr12:82449079
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1479-7648G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82449079 | ||||||
| chr12:82449188
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1479-7539T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82449188 | ||||||
| chr12:82449223
|
C | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 6 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1479-7504C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82449223 | ||||||
| chr12:82449257
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1479-7470T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82449257 | ||||||
| chr12:82449465
|
C | T | 1 | a0004c0004t0002g0093 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1479-7262C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82449465 | ||||||
| chr12:82449734
|
G | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1479-6993G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82449734 | ||||||
| chr12:82449802
|
C | A | 3 | a0005c0007t0001g0024a0005c0007t0001g0046a0005c0007t0001g0047 | 3 | HG02976.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1479-6925C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82449802 | ||||||
| chr12:82449830
|
AC | A | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1479-6896delC | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82449830 | ||||||
| chr12:82449864
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1479-6863A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82449864 | ||||||
| chr12:82449874
|
A | G | 6 | a0002c0002t0002g0126a0002c0006t0002g0100a0002c0006t0002g0101others(3): Show | 6 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1479-6853A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82449874 | ||||||
| chr12:82450198
|
T | C | 2 | a0002c0002t0002g0104a0003c0003t0002g0124 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1479-6529T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82450198 | ||||||
| chr12:82450386
|
C | T | 2 | a0001c0001t0001g0058a0001c0005t0001g0007 | 2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1479-6341C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82450386 | ||||||
| chr12:82450747
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1479-5980G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82450747 | ||||||
| chr12:82450758
|
C | T | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1479-5969C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82450758 | ||||||
| chr12:82450824
|
T | TA | 2 | a0005c0007t0001g0046a0005c0007t0001g0047 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1479-5902dupA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82450824 | |||||
| chr12:82450898
|
T | G | 1 | a0002c0006t0004g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1479-5829T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82450898 | ||||||
| chr12:82450948
|
CA | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1479-5778delA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82450948 | ||||||
| chr12:82450998
|
T | C | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1479-5729T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82450998 | ||||||
| chr12:82451258
|
C | T | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1479-5469C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82451258 | ||||||
| chr12:82451428
|
C | T | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1479-5299C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82451428 | ||||||
| chr12:82451613
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1479-5114G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82451613 | ||||||
| chr12:82451884
|
C | T | 1 | a0002c0002t0002g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1479-4843C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82451884 | ||||||
| chr12:82452200
|
C | T | 7 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0050others(4): Show | 7 | HG00280.hp1 HG01433.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1479-4527C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82452200 | ||||||
| chr12:82452547
|
C | A | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1479-4180C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82452547 | ||||||
| chr12:82453030
|
G | C | 1 | a0001c0001t0001g0083 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1479-3697G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82453030 | ||||||
| chr12:82453079
|
C | T | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1479-3648C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82453079 | ||||||
| chr12:82453811
|
C | A | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1479-2916C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82453811 | ||||||
| chr12:82453844
|
T | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1479-2883T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82453844 | ||||||
| chr12:82454189
|
AAAG | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0081 | 2 | HG01516.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1479-2533_1479-253 others(7): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82454189 | |||||
| chr12:82454238
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1479-2489C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82454238 | ||||||
| chr12:82454446
|
T | G | 1 | a0001c0005t0001g0007 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1479-2281T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82454446 | ||||||
| chr12:82454831
|
C | A | 8 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1479-1896C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82454831 | ||||||
| chr12:82454914
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1479-1813G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82454914 | ||||||
| chr12:82455161
|
TA | T | 12 | a0001c0001t0001g0038a0001c0001t0001g0070a0001c0001t0001g0083others(9): Show | 12 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1479-1553delA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 82455161 | |||||
| chr12:82455576
|
T | A | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1479-1151T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82455576 | ||||||
| chr12:82456648
|
A | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1479-79A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82456648 | ||||||
| chr12:82456650
|
A | G | 1 | a0002c0002t0002g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1479-77A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82456650 | ||||||
| chr12:82456846
|
T | G | 1 | a0001c0001t0001g0036 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1572+26T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82456846 | ||||||
| chr12:82457097
|
C | G | 1 | a0002c0006t0002g0101 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1572+277C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82457097 | ||||||
| chr12:82457331
|
G | GA | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1572+520dupA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 82457331 | |||||
| chr12:82457576
|
A | G | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+756A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82457576 | ||||||
| chr12:82457587
|
A | G | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1572+767A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82457587 | ||||||
| chr12:82457677
|
C | T | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1572+857C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82457677 | ||||||
| chr12:82457893
|
A | T | 1 | a0003c0003t0002g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1572+1073A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82457893 | ||||||
| chr12:82457958
|
T | C | 2 | a0001c0001t0001g0058a0001c0005t0001g0007 | 2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1572+1138T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82457958 | ||||||
| chr12:82458017
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1572+1197A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82458017 | ||||||
| chr12:82458365
|
A | T | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1572+1545A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82458365 | ||||||
| chr12:82458406
|
C | T | 8 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1572+1586C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82458406 | ||||||
| chr12:82458427
|
G | C | 1 | a0003c0003t0001g0107 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1572+1607G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82458427 | ||||||
| chr12:82458437
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0064 | 2 | HG02523.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1572+1617A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82458437 | ||||||
| chr12:82458439
|
T | G | 8 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1572+1619T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82458439 | ||||||
| chr12:82458518
|
T | C | 1 | a0006c0012t0001g0045 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1572+1698T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82458518 | ||||||
| chr12:82458607
|
A | G | 4 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090others(1): Show | 4 | HG01884.hp2 HG02109.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572+1787A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82458607 | ||||||
| chr12:82458665
|
A | G | 19 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(16): Show | 20 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1572+1845A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82458665 | ||||||
| chr12:82458843
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1572+2023A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82458843 | ||||||
| chr12:82458909
|
C | T | 3 | a0005c0007t0001g0024a0005c0007t0001g0046a0005c0007t0001g0047 | 3 | HG02976.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1572+2089C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82458909 | ||||||
| chr12:82459259
|
G | A | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1572+2439G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82459259 | ||||||
| chr12:82459343
|
G | A | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1572+2523G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82459343 | ||||||
| chr12:82459746
|
A | G | 6 | a0002c0002t0002g0126a0002c0006t0002g0100a0002c0006t0002g0101others(3): Show | 6 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1572+2926A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82459746 | ||||||
| chr12:82459828
|
C | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 7 | HG00280.hp2 HG01358.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.1572+3008C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82459828 | ||||||
| chr12:82459935
|
A | G | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1572+3115A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82459935 | ||||||
| chr12:82459990
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1572+3170C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82459990 | ||||||
| chr12:82460381
|
TAGTG | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1572+3563_1572+356 others(8): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 82460381 | |||||
| chr12:82460669
|
G | T | 2 | a0002c0002t0002g0104a0003c0003t0002g0124 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1572+3849G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82460669 | ||||||
| chr12:82460882
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1572+4062G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82460882 | ||||||
| chr12:82460931
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572+4111T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82460931 | ||||||
| chr12:82460939
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1572+4119G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82460939 | ||||||
| chr12:82460947
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1572+4127T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82460947 | ||||||
| chr12:82461012
|
G | A | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG00280.hp1 HG01433.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1572+4192G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82461012 | ||||||
| chr12:82461012
|
G | T | 2 | a0002c0002t0002g0104a0003c0003t0002g0124 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1572+4192G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82461012 | ||||||
| chr12:82461105
|
T | C | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0032others(2): Show | 5 | HG00280.hp2 HG01358.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.1572+4285T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82461105 | ||||||
| chr12:82461160
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1572+4340A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82461160 | ||||||
| chr12:82461243
|
A | G | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+4423A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82461243 | ||||||
| chr12:82461294
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1572+4474G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82461294 | ||||||
| chr12:82461299
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1572+4479T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82461299 | ||||||
| chr12:82461422
|
A | G | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(90): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1572+4602A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82461422 | ||||||
| chr12:82461529
|
ATATAACT others(3): Show |
A | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1572+4712_1572+472 others(14): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 82461529 | |||||
| chr12:82461582
|
A | C | 1 | a0001c0001t0001g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1572+4762A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82461582 | ||||||
| chr12:82461710
|
C | CA | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1572+4899dupA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 82461710 | |||||
| chr12:82461859
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0067 | 2 | NA18959.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1572+5039A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82461859 | ||||||
| chr12:82461932
|
C | A | 1 | a0003c0008t0001g0117 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1572+5112C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82461932 | ||||||
| chr12:82462129
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0070 | 2 | HG01978.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1572+5309A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82462129 | ||||||
| chr12:82462175
|
G | A | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1572+5355G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82462175 | ||||||
| chr12:82462233
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1572+5413G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82462233 | ||||||
| chr12:82462401
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1572+5581A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82462401 | ||||||
| chr12:82462679
|
G | A | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+5859G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82462679 | ||||||
| chr12:82462825
|
G | C | 1 | a0008c0010t0001g0075 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1572+6005G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82462825 | ||||||
| chr12:82463131
|
C | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0070 | 2 | HG01978.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1572+6311C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82463131 | ||||||
| chr12:82463267
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1572+6447T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82463267 | ||||||
| chr12:82463340
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1572+6520G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82463340 | ||||||
| chr12:82463389
|
CAT | C | 2 | a0001c0005t0001g0001a0001c0005t0001g0069 | 4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+6570_1572+657 others(6): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82463389 | ||||||
| chr12:82463394
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1572+6574T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82463394 | ||||||
| chr12:82463395
|
G | A | 4 | a0001c0001t0001g0059a0001c0005t0001g0001a0001c0005t0001g0012others(1): Show | 6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1572+6575G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82463395 | ||||||
| chr12:82463696
|
C | A | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+6876C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82463696 | ||||||
| chr12:82463769
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1572+6949G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82463769 | ||||||
| chr12:82463820
|
T | G | 4 | a0003c0003t0001g0108a0003c0003t0001g0109a0003c0003t0001g0111others(1): Show | 4 | HG00738.hp2 HG01346.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572+7000T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82463820 | ||||||
| chr12:82463894
|
A | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0032others(1): Show | 4 | HG00280.hp2 HG01358.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572+7074A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82463894 | ||||||
| chr12:82463954
|
G | A | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1572+7134G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82463954 | ||||||
| chr12:82464150
|
C | T | 1 | a0002c0002t0002g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1572+7330C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82464150 | ||||||
| chr12:82464211
|
C | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1572+7391C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82464211 | ||||||
| chr12:82464213
|
A | T | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1572+7393A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82464213 | ||||||
| chr12:82464251
|
A | C | 1 | a0004c0004t0002g0097 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1572+7431A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82464251 | ||||||
| chr12:82464320
|
C | T | 1 | a0002c0002t0002g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1572+7500C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82464320 | ||||||
| chr12:82464486
|
C | A | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1572+7666C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82464486 | ||||||
| chr12:82464535
|
T | A | 1 | a0001c0001t0001g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1572+7715T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82464535 | ||||||
| chr12:82464645
|
G | A | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1572+7825G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82464645 | ||||||
| chr12:82464894
|
AT | A | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1572+8082delT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 82464894 | |||||
| chr12:82465134
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0120 | 3 | HG02572.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1572+8314T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82465134 | ||||||
| chr12:82465151
|
G | C | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(90): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1572+8331G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82465151 | ||||||
| chr12:82465168
|
C | A | 1 | a0005c0007t0001g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1572+8348C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82465168 | ||||||
| chr12:82465414
|
G | T | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1572+8594G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82465414 | ||||||
| chr12:82465838
|
T | C | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1572+9018T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82465838 | ||||||
| chr12:82465945
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0032others(1): Show | 4 | HG00280.hp2 HG01358.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572+9125G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82465945 | ||||||
| chr12:82465966
|
C | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1572+9146C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82465966 | ||||||
| chr12:82465991
|
G | GT | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1572+9184dupT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 82465991 | |||||
| chr12:82465991
|
G | GTT | 4 | a0001c0001t0003g0031a0002c0002t0002g0106a0002c0002t0002g0126others(1): Show | 4 | HG02630.hp1 HG03927.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572+9183_1572+918 others(6): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 82465991 | |||||
| chr12:82466063
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1572+9243T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82466063 | ||||||
| chr12:82466332
|
GT | G | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1572+9524delT | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 82466332 | |||||
| chr12:82466501
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1572+9681G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82466501 | ||||||
| chr12:82466533
|
T | C | 2 | a0002c0002t0002g0104a0003c0003t0002g0124 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1572+9713T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82466533 | ||||||
| chr12:82467465
|
G | A | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1573-9179G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82467465 | ||||||
| chr12:82467482
|
T | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1573-9162T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82467482 | ||||||
| chr12:82467569
|
T | A | 1 | a0001c0001t0001g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1573-9075T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82467569 | ||||||
| chr12:82467648
|
C | T | 1 | a0002c0002t0002g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1573-8996C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82467648 | ||||||
| chr12:82467655
|
C | T | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1573-8989C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82467655 | ||||||
| chr12:82467761
|
G | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0032others(1): Show | 4 | HG00280.hp2 HG01358.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1573-8883G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82467761 | ||||||
| chr12:82467883
|
C | A | 1 | a0002c0002t0002g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1573-8761C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82467883 | ||||||
| chr12:82467949
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1573-8695G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82467949 | ||||||
| chr12:82468075
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1573-8569C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82468075 | ||||||
| chr12:82468424
|
C | G | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1573-8220C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82468424 | ||||||
| chr12:82468491
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1573-8153C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82468491 | ||||||
| chr12:82468714
|
G | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062 | 3 | HG02280.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1573-7930G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82468714 | ||||||
| chr12:82469309
|
C | T | 2 | a0002c0002t0002g0106a0002c0002t0002g0126 | 2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1573-7335C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82469309 | ||||||
| chr12:82469879
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1573-6765A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82469879 | ||||||
| chr12:82470047
|
A | G | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1573-6597A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82470047 | ||||||
| chr12:82470067
|
C | G | 42 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(39): Show | 44 | HG00099.hp2 HG00738.hp2 HG01256.hp2 others(41): Show |
intron_variant | MODIFIER | c.1573-6577C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82470067 | ||||||
| chr12:82470139
|
T | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(39): Show | 44 | HG00099.hp2 HG00738.hp2 HG01256.hp2 others(41): Show |
intron_variant | MODIFIER | c.1573-6505T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82470139 | ||||||
| chr12:82470353
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1573-6291G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82470353 | ||||||
| chr12:82470545
|
TACAGGGC others(13): Show |
T | 26 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(23): Show | 27 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.1573-6082_1573-606 others(24): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 82470545 | |||||
| chr12:82470623
|
C | G | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1573-6021C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82470623 | ||||||
| chr12:82470988
|
T | A | 2 | a0002c0002t0002g0106a0002c0002t0002g0126 | 2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1573-5656T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82470988 | ||||||
| chr12:82470995
|
G | A | 13 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(10): Show | 13 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.1573-5649G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82470995 | ||||||
| chr12:82471226
|
C | T | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1573-5418C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82471226 | ||||||
| chr12:82471513
|
A | C | 1 | a0001c0001t0001g0005 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1573-5131A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82471513 | ||||||
| chr12:82471793
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1573-4851C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82471793 | ||||||
| chr12:82471916
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1573-4728G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82471916 | ||||||
| chr12:82471983
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1573-4661A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82471983 | ||||||
| chr12:82472080
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1573-4564C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82472080 | ||||||
| chr12:82472086
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1573-4558G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82472086 | ||||||
| chr12:82472134
|
C | T | 26 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(23): Show | 27 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.1573-4510C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82472134 | ||||||
| chr12:82472295
|
T | C | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1573-4349T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82472295 | ||||||
| chr12:82472370
|
A | G | 42 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(39): Show | 44 | HG00099.hp2 HG00738.hp2 HG01256.hp2 others(41): Show |
intron_variant | MODIFIER | c.1573-4274A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82472370 | ||||||
| chr12:82472461
|
G | T | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1573-4183G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82472461 | ||||||
| chr12:82472526
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1573-4118A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82472526 | ||||||
| chr12:82472598
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1573-4046G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82472598 | ||||||
| chr12:82472601
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1573-4043A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82472601 | ||||||
| chr12:82472606
|
A | G | 1 | a0003c0003t0001g0109 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1573-4038A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82472606 | ||||||
| chr12:82472644
|
A | G | 1 | a0002c0002t0002g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1573-4000A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82472644 | ||||||
| chr12:82472844
|
G | C | 14 | a0001c0001t0001g0040a0002c0006t0002g0100a0002c0006t0002g0101others(11): Show | 14 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.1573-3800G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82472844 | ||||||
| chr12:82472860
|
C | T | 27 | a0001c0001t0001g0040a0002c0002t0002g0002a0002c0002t0002g0085others(24): Show | 28 | HG01256.hp2 HG01361.hp1 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.1573-3784C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82472860 | ||||||
| chr12:82472864
|
G | A | 1 | a0009c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1573-3780G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82472864 | ||||||
| chr12:82473366
|
T | G | 10 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1573-3278T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82473366 | ||||||
| chr12:82473492
|
A | C | 1 | a0001c0001t0001g0067 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1573-3152A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82473492 | ||||||
| chr12:82473505
|
G | T | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1573-3139G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82473505 | ||||||
| chr12:82473578
|
T | C | 2 | a0002c0002t0002g0106a0002c0002t0002g0126 | 2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1573-3066T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82473578 | ||||||
| chr12:82473590
|
T | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1573-3054T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82473590 | ||||||
| chr12:82473688
|
A | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1573-2956A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82473688 | ||||||
| chr12:82474099
|
T | A | 1 | a0001c0001t0001g0055 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1573-2545T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82474099 | ||||||
| chr12:82474299
|
A | G | 2 | a0001c0001t0001g0058a0001c0005t0001g0007 | 2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1573-2345A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82474299 | ||||||
| chr12:82474496
|
T | C | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1573-2148T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82474496 | ||||||
| chr12:82474569
|
ACTT | A | 4 | a0002c0002t0002g0002a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1573-2071_1573-206 others(7): Show |
METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 82474569 | |||||
| chr12:82474717
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1573-1927T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82474717 | ||||||
| chr12:82474965
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1573-1679A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82474965 | ||||||
| chr12:82474994
|
G | A | 8 | a0004c0004t0002g0093a0004c0004t0002g0094a0004c0004t0002g0095others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1573-1650G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82474994 | ||||||
| chr12:82475381
|
G | C | 4 | a0003c0003t0001g0108a0003c0003t0001g0109a0003c0003t0001g0110others(1): Show | 4 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1573-1263G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82475381 | ||||||
| chr12:82475650
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1573-994G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82475650 | ||||||
| chr12:82475706
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1573-938A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82475706 | ||||||
| chr12:82475862
|
T | G | 3 | a0003c0003t0001g0107a0003c0003t0001g0113a0003c0003t0001g0114 | 3 | HG01891.hp1 NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1573-782T>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82475862 | ||||||
| chr12:82476204
|
T | C | 2 | a0002c0002t0002g0106a0002c0002t0002g0126 | 2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1573-440T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82476204 | ||||||
| chr12:82476218
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0030others(5): Show | 8 | HG01257.hp1 HG01516.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1573-426A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82476218 | ||||||
| chr12:82476419
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(39): Show | 44 | HG00099.hp2 HG00738.hp2 HG01256.hp2 others(41): Show |
intron_variant | MODIFIER | c.1573-225G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82476419 | ||||||
| chr12:82476763
|
C | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0120others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1647+45C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 10/11 | chr12 | 82476763 | ||||||
| chr12:82477376
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1719+24C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 11/11 | chr12 | 82477376 | ||||||
| chr12:82477454
|
A | T | 3 | a0002c0002t0002g0088a0002c0002t0002g0089a0002c0002t0002g0090 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1719+102A>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 11/11 | chr12 | 82477454 | ||||||
| chr12:82477605
|
G | T | 6 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(3): Show | 6 | HG01256.hp2 HG01358.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1719+253G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 11/11 | chr12 | 82477605 | ||||||
| chr12:82477656
|
G | T | 1 | a0002c0002t0002g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1719+304G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 11/11 | chr12 | 82477656 | ||||||
| chr12:82477949
|
C | T | 9 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(6): Show | 9 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1719+597C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 11/11 | chr12 | 82477949 | ||||||
| chr12:82478667
|
T | A | 9 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(6): Show | 9 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720-265T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 11/11 | chr12 | 82478667 | ||||||
| chr12:82478684
|
C | T | 9 | a0003c0003t0001g0107a0003c0003t0001g0108a0003c0003t0001g0109others(6): Show | 9 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720-248C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 11/11 | chr12 | 82478684 | ||||||
| chr12:82478797
|
TA | T | 6 | a0002c0006t0002g0100a0002c0006t0002g0101a0002c0006t0002g0102others(3): Show | 6 | HG01256.hp2 HG01358.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1720-133delA | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr12 | 82478797 | |||||
| chr12:82478919
|
T | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0052 | 2 | HG01433.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1720-13T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 11/11 | chr12 | 82478919 |