Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MAASC others(598): Show |
chr12 | 82353529 | 82484239 |
| a0002 | 1/0 | 603 | 18 | 13 | 2 | 0 | 2 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | MAASC others(598): Show |
chr12 | 82353529 | 82484239 |
| a0003 | 0/0 | 603 | 12 | 2 | 3 | 1 | 2 | 4 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | MAASC others(598): Show |
chr12 | 82353529 | 82484239 |
| a0004 | 0/0 | 603 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | MAASC others(598): Show |
chr12 | 82353529 | 82484239 |
| a0005 | 0/0 | 603 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | MAASC others(598): Show |
chr12 | 82353529 | 82484239 |
| a0006 | 0/0 | 603 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | MAASC others(598): Show |
chr12 | 82353529 | 82484239 |
| a0007 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | MAASC others(598): Show |
chr12 | 82353529 | 82484239 |
| a0008 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | MAASC others(598): Show |
chr12 | 82353529 | 82484239 |
| a0009 | 0/1 | 603 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | MAASC others(598): Show |
chr12 | 82353529 | 82484239 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1809 | 80 | 33 | 17 | 12 | 6 | 12 | METTL25_chr12_82353529_82484239 | METTL25 | ATGGC others(1804): Show |
chr12 | 82353529 | 82484239 | ||
| a0001c0005 | 0/0 | 1809 | 6 | 6 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGGC others(1804): Show |
chr12 | 82353529 | 82484239 | ||
| a0002c0002 | 1/0 | 1809 | 13 | 12 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGGC others(1804): Show |
chr12 | 82353529 | 82484239 | ||
| a0002c0006 | 0/0 | 1809 | 5 | 1 | 2 | 0 | 2 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGGC others(1804): Show |
chr12 | 82353529 | 82484239 | ||
| a0003c0003 | 0/0 | 1809 | 11 | 2 | 3 | 1 | 2 | 3 | METTL25_chr12_82353529_82484239 | METTL25 | ATGGC others(1804): Show |
chr12 | 82353529 | 82484239 | ||
| a0003c0008 | 0/0 | 1809 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | ATGGC others(1804): Show |
chr12 | 82353529 | 82484239 | ||
| a0004c0004 | 0/0 | 1809 | 7 | 7 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGGC others(1804): Show |
chr12 | 82353529 | 82484239 | ||
| a0005c0007 | 0/0 | 1809 | 3 | 3 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGGC others(1804): Show |
chr12 | 82353529 | 82484239 | ||
| a0006c0012 | 0/0 | 1809 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGGC others(1804): Show |
chr12 | 82353529 | 82484239 | ||
| a0007c0011 | 0/0 | 1809 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGGC others(1804): Show |
chr12 | 82353529 | 82484239 | ||
| a0008c0009 | 0/0 | 1809 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGGC others(1804): Show |
chr12 | 82353529 | 82484239 | ||
| a0009c0010 | 0/1 | 1809 | 1 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGGC others(1804): Show |
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 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| a0001c0001t0003 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| a0001c0005t0001 | 0/0 | 2064 | 6 | 6 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| a0002c0002t0001 | 1/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| a0002c0002t0002 | 0/0 | 2064 | 12 | 12 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| a0002c0006t0002 | 0/0 | 2064 | 4 | 0 | 2 | 0 | 2 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| a0002c0006t0004 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| a0003c0003t0001 | 0/0 | 2064 | 9 | 1 | 2 | 1 | 2 | 3 | METTL25_chr12_82353529_82484239 | METTL25 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| a0003c0003t0002 | 0/0 | 2064 | 2 | 1 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| a0003c0008t0001 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| a0004c0004t0002 | 0/0 | 2064 | 7 | 7 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| a0005c0007t0001 | 0/0 | 2064 | 3 | 3 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| a0006c0012t0001 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| a0007c0011t0002 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| a0008c0009t0002 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| a0009c0010t0001 | 0/1 | 2064 | 1 | 0 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | ATGTT others(2059): Show |
chr12 | 82353529 | 82484239 |
| actghapid | grch38/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 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0001g0075 | 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 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0001t0003g0033 | 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 |
| a0001c0005t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0005t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0001c0005t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0002t0001g0104 | 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 |
| a0002c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0002c0002t0002g0107 | 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 |
| a0002c0006t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0003t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0003c0008t0001g0118 | 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 |
| a0005c0007t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0005c0007t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0006c0012t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0007c0011t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0008c0009t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| a0009c0010t0001g0005 | 0/1 | 1 | 0 | 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 | g0018 | EUR | GBR | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG00099 | hp2 | a0003 | c0003 | t0001 | g0111 | EUR | GBR | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | FIN | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0029 | 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 | g0040 | EAS | CHS | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG00738 | hp2 | a0003 | c0003 | t0001 | g0109 | AMR | PUR | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0069 | 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 | g0037 | 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 | g0112 | 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 | g0113 | AMR | CLM | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0034 | 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 | g0007 | AMR | CLM | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0017 | 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 | g0030 | 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 | g0016 | EUR | IBS | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0122 | 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 | g0108 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0120 | 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 | g0045 | AMR | PEL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02055 | hp1 | a0003 | c0003 | t0002 | g0125 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0031 | 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 | g0116 | 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 | g0028 | AMR | PEL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0011 | 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 | g0062 | AFR | ACB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0071 | 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 | g0046 | 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 | g0075 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0107 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02630 | hp2 | a0002 | c0006 | t0004 | g0106 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0052 | 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 | g0124 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02735 | hp2 | a0003 | c0008 | t0001 | g0118 | 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 | g0006 | 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 | g0042 | AFR | GWD | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0064 | 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 | g0060 | 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 | g0121 | 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 | g0055 | 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 | g0010 | AFR | ESN | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03139 | hp2 | a0001 | c0005 | t0001 | g0013 | AFR | ESN | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0105 | 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 | g0061 | AFR | MSL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03516 | hp1 | a0005 | c0007 | t0001 | g0047 | 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 | g0032 | SAS | PJL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03710 | hp1 | a0003 | c0003 | t0001 | g0117 | SAS | PJL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03927 | hp1 | a0003 | c0003 | t0001 | g0110 | SAS | BEB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0033 | SAS | BEB | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA18522 | hp1 | a0005 | c0007 | t0001 | g0048 | 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 | g0070 | AFR | YRI | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0074 | 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 | g0072 | EAS | JPT | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0066 | 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 | g0041 | AFR | ASW | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | TSI | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA20752 | hp2 | a0003 | c0003 | t0001 | g0114 | EUR | TSI | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA20905 | hp1 | a0003 | c0003 | t0001 | g0115 | SAS | GIH | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0027 | 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 | g0067 | 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 | g0008 | 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 | g0063 | AFR | USA | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | USA | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| NA21309 | hp2 | a0008 | c0009 | t0002 | g0091 | AFR | LWK | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| homoSapiens | chm13v2 | a0009 | c0010 | t0001 | g0005 | REF | REF | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0104 | REF | REF | METTL25_chr12_82353529_82484239 | METTL25 | chr12 | 82353529 | 82484239 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | 5 | a0001 a0003 a0005 others(2): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | |||
| chr12:82430950 | G | T | 2 | a0004 a0007 |
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 | a0008 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | 7 | a0001c0001 a0001c0005 a0003c0003 others(4): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0002c0002t0002 a0002c0006t0002 a0002c0006t0004 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:82358854 | G | A | 80 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
82 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(79): 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 | |||||||
| chr12:82359460 | C | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0006 | 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.259+949A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82359773 | |||||||
| chr12:82359867 | T | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0120 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.259+1696A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82360520 | |||||||
| chr12:82360602 | G | A | 1 | a0001c0001t0001g0007 | 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 others(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 | a0001c0005t0001g0008 | 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 | |||||||
| chr12:82361037 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0107 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | |||||||
| chr12:82361414 | 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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.259+2651C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82361475 | |||||||
| chr12:82361512 | G | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0008c0009t0002g0091 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0001g0108 | 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0001c0001t0001g0011 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.259+3512G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82362336 | |||||||
| 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 | a0001c0001t0001g0012 | 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 | a0001c0005t0001g0013 | 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 | |||||||
| chr12:82363731 | T | TA | 79 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(77): 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 | a0003c0003t0001g0109 a0003c0003t0001g0110 a0003c0003t0001g0111 others(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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0002c0006t0004g0106 | 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 | a0001c0001t0001g0010 | 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 | a0002c0002t0002g0092 a0002c0002t0002g0107 a0002c0006t0002g0100 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(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 | a0003c0003t0002g0125 | 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0001c0001t0001g0019 | 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 | a0003c0003t0002g0125 | 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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0001c0001t0001g0026 | 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | |||||||
| chr12:82366089 | T | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0003c0003t0001g0109 a0003c0003t0001g0110 a0003c0003t0001g0111 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 others(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 | a0001c0001t0001g0007 | 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 | a0002c0002t0002g0092 a0002c0002t0002g0107 a0002c0006t0002g0100 others(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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | |||||||
| chr12:82368030 | 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0001c0001t0001g0054 a0003c0003t0001g0108 a0003c0003t0001g0109 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0002c0002t0002g0105 | 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0064 | 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0002c0002t0002g0092 a0002c0002t0002g0107 a0002c0006t0002g0100 others(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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.259+10506G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82369330 | |||||||
| chr12:82369519 | A | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.259+10695A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82369519 | |||||||
| chr12:82369620 | G | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.259+10796G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82369620 | |||||||
| chr12:82369785 | TTG | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0002c0002t0002g0107 | 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 | a0002c0006t0004g0106 | 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 | a0002c0002t0002g0092 a0002c0002t0002g0107 a0002c0006t0002g0100 others(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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): 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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): 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 | a0002c0002t0002g0107 | 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.259+12220A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82371044 | |||||||
| chr12:82371328 | C | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 others(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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0005c0007t0001g0047 a0005c0007t0001g0048 |
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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0002c0002t0002g0092 a0004c0004t0002g0093 a0004c0004t0002g0094 others(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 | a0001c0001t0001g0075 | 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 | a0006c0012t0001g0046 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.259+13113G>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82371937 | |||||||
| chr12:82372129 | C | T | 1 | a0002c0002t0002g0105 | 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0001c0001t0001g0011 a0001c0001t0001g0045 |
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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0001c0001t0001g0014 | 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0008c0009t0002g0091 | 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0001c0001t0001g0043 | 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): 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 | a0001c0005t0001g0013 | 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 | a0001c0001t0001g0011 | 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 | a0008c0009t0002g0091 | 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 | a0002c0002t0002g0107 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0012 | 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 | a0002c0002t0002g0107 | 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0001c0001t0001g0065 | 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | 84 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 others(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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0105 | 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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.260-10882G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82375921 | |||||||
| chr12:82375932 | A | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0001c0001t0001g0055 a0001c0001t0001g0064 |
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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0001c0001t0001g0042 | 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0055 a0001c0001t0001g0056 others(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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | |||||||
| chr12:82376418 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 |
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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.260-10088C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82376715 | |||||||
| chr12:82376854 | A | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0001c0001t0001g0040 | 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 | a0002c0002t0002g0092 a0002c0002t0002g0107 a0002c0006t0002g0100 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0071 others(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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0105 | 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 | a0002c0002t0002g0107 | 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 | a0002c0002t0002g0092 a0002c0002t0002g0107 a0002c0006t0002g0100 others(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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.260-8039C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82378764 | |||||||
| chr12:82378816 | T | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0064 |
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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0008c0009t0002g0091 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0105 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0121 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
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 | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(99): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): 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 | |||||||
| chr12:82380239 | G | C | 3 | a0003c0003t0001g0108 a0003c0003t0001g0114 a0003c0003t0001g0115 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(99): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): 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 | a0001c0001t0001g0055 | 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 | a0002c0002t0002g0107 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0002c0002t0002g0105 | 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 | a0001c0001t0001g0007 a0002c0002t0002g0126 |
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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0038 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 |
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 | a0001c0001t0001g0054 | 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0001c0005t0001g0001 a0001c0005t0001g0070 |
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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): 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 | a0008c0009t0002g0091 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0066 a0002c0006t0002g0100 a0002c0006t0002g0101 others(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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): 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 | a0008c0009t0002g0091 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0071 others(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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.260-2236A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 1/11 | chr12 | 82384567 | |||||||
| chr12:82384602 | A | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0002c0002t0002g0092 a0003c0003t0001g0108 a0003c0003t0001g0109 others(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 | a0003c0003t0001g0117 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0084 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0001c0001t0001g0075 | 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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0105 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | |||||||
| chr12:82385198 | C | A | 6 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0066 | 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | 56 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(53): Show |
56 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(53): 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0003c0003t0002g0125 | 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 | a0002c0002t0002g0087 a0002c0002t0002g0088 a0002c0002t0002g0089 others(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 | a0003c0003t0002g0125 | 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0001c0001t0001g0056 a0003c0003t0001g0108 a0003c0003t0001g0109 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | |||||||
| chr12:82386533 | T | G | 1 | a0003c0003t0001g0114 | 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 | a0001c0001t0001g0007 | 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 | a0002c0006t0004g0106 | 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 | a0001c0001t0001g0012 | 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0107 | 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 | 79 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(76): Show |
81 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(78): 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 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0023 a0003c0003t0001g0108 a0003c0003t0001g0109 others(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 | a0001c0001t0001g0055 a0003c0003t0001g0110 |
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 | a0003c0003t0001g0115 | 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 | a0002c0002t0002g0105 | 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 | a0001c0001t0001g0051 | 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0001c0001t0001g0027 | 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | |||||||
| chr12:82389281 | G | GA | 4 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(106): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(109): 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0011 | 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 | a0002c0002t0002g0105 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0018 | 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 | ATGTGTG | 23 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0105 | 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 | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(119): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0002c0006t0002g0100 a0002c0006t0002g0102 a0002c0006t0002g0103 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): 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 | a0008c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.531+2159T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82392081 | |||||||
| chr12:82392194 | C | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0001c0001t0001g0006 | 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | |||||||
| chr12:82393677 | TG | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0107 a0004c0004t0002g0093 a0004c0004t0002g0094 others(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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0045 | 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.531+4370A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82394292 | |||||||
| chr12:82394319 | A | G | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0001c0001t0001g0037 | 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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0002c0002t0002g0107 | 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 | a0002c0002t0002g0105 | 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0002c0002t0002g0107 a0004c0004t0002g0093 a0004c0004t0002g0094 others(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 | a0002c0002t0002g0107 | 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 | a0003c0003t0001g0109 a0003c0003t0001g0112 a0003c0003t0002g0113 |
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 | a0002c0002t0002g0107 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.532-1504A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 3/11 | chr12 | 82397291 | |||||||
| chr12:82397293 | A | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0008c0009t0002g0091 | 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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0008c0009t0002g0091 | 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 | a0002c0002t0002g0105 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0006 | 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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | 80 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
82 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(79): 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1131+749G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 4/11 | chr12 | 82400143 | |||||||
| chr12:82400175 | A | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(104): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(107): 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | 18 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0015 others(15): Show |
18 | HG00099.hp1 HG00673.hp1 HG01257.hp1 others(15): 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 | a0001c0001t0001g0061 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | TAAAAA | 55 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(52): Show |
55 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(52): 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0105 | 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0002c0002t0002g0105 | 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0001c0001t0001g0041 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0008c0009t0002g0091 | 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0005c0007t0001g0048 | 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0107 | 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 | a0002c0002t0002g0107 | 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0017 | 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 | a0003c0003t0001g0110 | 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0071 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | 88 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
90 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(87): 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0040 others(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 | |||||||
| chr12:82406749 | C | T | 1 | a0002c0002t0002g0107 | 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 | a0001c0001t0001g0057 | 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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): 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 | a0002c0002t0002g0105 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0001c0001t0001g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1279+4177G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82407307 | |||||||
| chr12:82407517 | C | G | 1 | a0002c0002t0002g0107 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0064 |
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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0002c0002t0002g0105 | 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 | a0001c0001t0001g0060 a0003c0003t0001g0108 a0003c0003t0001g0109 others(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 | CGTGTGTG others(1): Show |
21 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0026 others(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 | a0001c0005t0001g0070 a0002c0002t0002g0086 a0002c0002t0002g0092 others(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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | 80 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
82 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(79): 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 | a0002c0002t0002g0105 | 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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1279+6164G>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82409294 | |||||||
| chr12:82409404 | A | T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): 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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | 80 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
82 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(79): 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0002c0002t0002g0105 | 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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0001c0001t0001g0120 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0003c0003t0001g0109 a0003c0003t0001g0112 a0003c0003t0002g0113 |
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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0052 | 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 | a0002c0002t0002g0107 a0002c0006t0002g0100 a0002c0006t0002g0101 others(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 | a0005c0007t0001g0047 a0005c0007t0001g0048 |
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 | a0008c0009t0002g0091 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): 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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0002c0002t0002g0107 a0002c0006t0002g0100 a0002c0006t0002g0101 others(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 | a0001c0001t0001g0056 | 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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0006c0012t0001g0046 | 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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0003c0003t0001g0109 a0003c0003t0001g0110 a0003c0003t0001g0111 others(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 | a0002c0002t0002g0105 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0071 |
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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): 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 | a0002c0002t0002g0107 a0002c0006t0002g0100 a0002c0006t0002g0101 others(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 | 81 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(78): Show |
83 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(80): 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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): 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 | a0008c0009t0002g0091 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0050 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0054 |
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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0052 a0002c0002t0002g0107 |
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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0034 others(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 | a0005c0007t0001g0048 | 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 | a0002c0002t0002g0107 | 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 | a0003c0003t0001g0117 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0008c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1280-12830A>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82418063 | |||||||
| chr12:82418368 | G | C | 1 | a0003c0003t0002g0125 | 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0002c0002t0002g0107 | 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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0002c0006t0002g0100 a0002c0006t0002g0102 a0002c0006t0002g0103 |
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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0042 others(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 | 92 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(89): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): 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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0068 |
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 | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): 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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0084 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): 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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1280-9842G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82421051 | |||||||
| chr12:82421208 | G | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1280-9685G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82421208 | |||||||
| chr12:82421518 | A | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1280-9375A>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82421518 | |||||||
| chr12:82421581 | T | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1280-9312T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82421581 | |||||||
| chr12:82421600 | C | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0041 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1280-8544C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82422349 | |||||||
| chr12:82422582 | A | G | 1 | a0006c0012t0001g0046 | 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 | a0002c0002t0002g0107 | 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 | a0001c0001t0001g0007 | 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 | a0003c0003t0002g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1280-7941G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 5/11 | chr12 | 82422952 | |||||||
| 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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0002c0002t0002g0107 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | |||||||
| chr12:82423495 | 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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0063 | 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 | a0002c0002t0002g0105 | 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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0005t0001g0013 | 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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0115 |
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 | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(91): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0080 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0080 |
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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0002c0002t0002g0105 | 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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0003c0003t0001g0110 | 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 | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): 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 | a0008c0009t0002g0091 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): 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 | a0002c0006t0004g0106 | 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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0034 others(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 | |||||||
| chr12:82427805 | AT | A | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 others(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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0001c0001t0001g0069 | 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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): 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 | a0001c0001t0001g0026 a0001c0001t0001g0049 a0001c0001t0001g0054 others(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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0001c0001t0001g0023 a0002c0002t0002g0092 a0002c0002t0002g0107 others(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 | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(87): Show |
93 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(90): 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 | a0008c0009t0002g0091 | 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 | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(115): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0052 | 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 | |||||||
| chr12:82431916 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0002c0002t0002g0107 | 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | |||||||
| chr12:82432811 | 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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
85 | HG00099.hp1 HG00673.hp1 HG00673.hp2 others(82): 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 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0038 others(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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0003c0003t0001g0116 | 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0003c0003t0001g0108 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | |||||||
| chr12:82435045 | C | T | 11 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0075 | 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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0036 | 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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1404+1231C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 7/11 | chr12 | 82435955 | |||||||
| chr12:82436069 | G | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0002c0006t0002g0100 |
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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 |
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 | a0003c0003t0002g0125 | 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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 |
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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0120 a0003c0003t0002g0125 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 others(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 | ||||||
| chr12:82438673 | G | GT | 4 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0031 | 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 | a0008c0009t0002g0091 | 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 | |||||||
| chr12:82440097 | A | G | 1 | a0001c0001t0001g0043 | 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 | 93 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(90): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): 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 | a0001c0001t0001g0019 a0001c0001t0001g0068 |
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 | a0001c0001t0001g0038 | 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0002c0002t0002g0105 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0002c0002t0002g0126 a0003c0003t0001g0108 a0003c0003t0001g0109 others(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 | 79 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(76): Show |
81 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(78): 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 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0061 |
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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0001c0001t0001g0011 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1478+2676T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82441467 | |||||||
| 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 | a0002c0002t0002g0105 | 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 | a0001c0001t0001g0064 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0001c0001t0001g0042 a0004c0004t0002g0093 a0004c0004t0002g0094 others(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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0001c0001t0001g0031 a0002c0002t0002g0087 |
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 | a0001c0001t0001g0064 a0003c0003t0002g0125 a0003c0008t0001g0118 |
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 |
53 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(50): Show |
54 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(51): 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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0002c0002t0002g0002 others(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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0001c0001t0003g0033 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0066 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0022 |
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 | a0001c0001t0001g0061 | 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 | a0002c0002t0002g0107 | 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0111 others(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 | a0005c0007t0001g0024 a0005c0007t0001g0047 a0005c0007t0001g0048 |
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 | |||||||
| chr12:82442197 | 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 others(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 | 93 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(90): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): 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 | 93 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(90): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): 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 | ||||||
| chr12:82444503 | G | A | 1 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0065 |
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 | a0008c0009t0002g0091 | 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0008c0009t0002g0091 | 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 | a0008c0009t0002g0091 | 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 | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1478+7131G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82445922 | |||||||
| chr12:82446469 | C | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): 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 | a0001c0005t0001g0008 | 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 | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): 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 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0034 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0002c0002t0002g0107 | 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 | 92 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1478+7918C>T | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82446709 | |||||||
| 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1479-8790T>C | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82447937 | |||||||
| chr12:82447986 | A | G | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0071 |
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 | a0001c0001t0001g0006 | 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0001c0001t0001g0044 | 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 | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0054 | 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 | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(92): Show |
98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): 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 | a0005c0007t0001g0024 a0005c0007t0001g0047 a0005c0007t0001g0048 |
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 | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1479-6896delC | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82449830 | |||||||
| chr12:82449864 | A | G | 1 | a0001c0001t0001g0006 | 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 | a0002c0002t0002g0126 a0002c0006t0002g0100 a0002c0006t0002g0101 others(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 | a0002c0002t0002g0105 a0003c0003t0002g0125 |
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 | a0001c0001t0001g0058 a0001c0005t0001g0008 |
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 | a0001c0001t0001g0042 | 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 | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): 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 | a0005c0007t0001g0047 a0005c0007t0001g0048 |
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 | a0002c0006t0004g0106 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0008c0009t0002g0091 | 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 | a0002c0002t0002g0107 | 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 | a0001c0001t0003g0033 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0051 others(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 | a0002c0002t0002g0107 | 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 | a0008c0009t0002g0091 | 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 | a0008c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1479-2916C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 8/11 | chr12 | 82453811 | |||||||
| chr12:82454189 | AAAG | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0081 |
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 | a0001c0001t0001g0041 | 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 | a0001c0005t0001g0008 | 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0001g0083 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): 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 | a0001c0001t0001g0031 | 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 | |||||||
| chr12:82457576 | A | G | 1 | a0008c0009t0002g0091 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0002g0125 | 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 | a0001c0001t0001g0058 a0001c0005t0001g0008 |
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 | a0001c0001t0001g0072 | 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 | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0003c0003t0001g0108 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0065 |
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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0006c0012t0001g0046 | 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0001c0001t0001g0040 | 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 | a0005c0007t0001g0024 a0005c0007t0001g0047 a0005c0007t0001g0048 |
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 | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0002c0002t0002g0126 a0002c0006t0002g0100 a0002c0006t0002g0101 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0105 a0003c0003t0002g0125 |
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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0002c0002t0002g0105 a0003c0003t0002g0125 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0040 | 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 | a0008c0009t0002g0091 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | |||||||
| chr12:82461422 | A | G | 92 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0052 | 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 | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): 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 | a0001c0001t0001g0019 a0001c0001t0001g0068 |
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 | a0003c0008t0001g0118 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0071 |
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 | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0008c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+5859G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82462679 | |||||||
| chr12:82463131 | C | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0071 |
2 | HG01978.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1572+6311C>G | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82463131 | |||||||
| chr12:82463340 | G | A | 1 | a0001c0001t0001g0043 | 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 | a0001c0005t0001g0001 a0001c0005t0001g0070 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
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 | a0001c0001t0001g0059 a0001c0005t0001g0001 a0001c0005t0001g0013 others(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 | a0008c0009t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1572+6876C>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82463696 | |||||||
| chr12:82463820 | T | G | 4 | a0003c0003t0001g0109 a0003c0003t0001g0110 a0003c0003t0001g0112 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0034 others(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 | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0107 | 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 | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): 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 | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.1572+7825G>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 9/11 | chr12 | 82464645 | |||||||
| chr12:82464894 | AT | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): 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 | a0001c0001t0001g0003 a0001c0001t0001g0121 |
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 | 92 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0002c0002t0002g0107 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0034 others(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 | 114 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(111): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): 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 | a0001c0001t0003g0033 a0002c0002t0002g0107 a0002c0002t0002g0126 others(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 | a0001c0001t0001g0055 | 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 | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): 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 | a0001c0001t0001g0054 | 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 | a0002c0002t0002g0105 a0003c0003t0002g0125 |
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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0052 | 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0019 | 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 | a0001c0001t0001g0031 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
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 | a0002c0002t0002g0107 a0002c0002t0002g0126 |
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 | a0001c0001t0001g0043 | 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 | a0002c0002t0002g0107 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0075 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0002c0002t0002g0107 a0002c0002t0002g0126 |
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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0002c0002t0002g0107 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0029 | 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 | a0003c0003t0001g0110 | 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 | a0001c0001t0001g0041 a0002c0006t0002g0100 a0002c0006t0002g0101 others(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 | a0001c0001t0001g0041 a0002c0002t0002g0002 a0002c0002t0002g0085 others(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 | a0008c0009t0002g0091 | 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0001c0001t0001g0068 | 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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0002c0002t0002g0107 a0002c0002t0002g0126 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0058 a0001c0005t0001g0008 |
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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0002c0002t0002g0002 a0002c0002t0002g0085 a0002c0002t0002g0086 others(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 | a0001c0001t0001g0010 | 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 | a0004c0004t0002g0093 a0004c0004t0002g0094 a0004c0004t0002g0095 others(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 | a0003c0003t0001g0109 a0003c0003t0001g0110 a0003c0003t0001g0111 others(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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0114 a0003c0003t0001g0115 |
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 | a0002c0002t0002g0107 a0002c0002t0002g0126 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0120 | 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 | a0002c0002t0002g0088 a0002c0002t0002g0089 a0002c0002t0002g0090 |
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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0002c0002t0002g0107 | 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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0003c0003t0001g0108 a0003c0003t0001g0109 a0003c0003t0001g0110 others(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 | a0002c0006t0002g0100 a0002c0006t0002g0101 a0002c0006t0002g0102 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0053 |
2 | HG01433.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1720-13T>A | METTL25 | ENSG00000127720.8 | transcript | ENST00000248306.8 | protein_coding | 11/11 | chr12 | 82478919 |