geneid | 79828 |
---|---|
ensemblid | ENSG00000123600.21 |
hgncid | 25856 |
symbol | METTL8 |
name | methyltransferase 8, tRNA N3-cytidine |
refseq_nuc | NM_001321154.2 |
refseq_prot | NP_001308083.1 |
ensembl_nuc | ENST00000375258.9 |
ensembl_prot | ENSP00000364407.4 |
mane_status | MANE Select |
chr | chr2 |
start | 171315746 |
end | 171433990 |
strand | - |
ver | v1.2 |
region | chr2:171315746-171433990 |
region5000 | chr2:171310746-171438990 |
regionname0 | METTL8_chr2_171315746_171433990 |
regionname5000 | METTL8_chr2_171310746_171438990 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 407 | 310 | 72 | 59 | 139 | 8 | 30 | 104 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0002 | 0/0 | 407 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0003 | 0/0 | 407 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0004 | 0/0 | 407 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0005 | 0/0 | 327 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0006 | 0/0 | 407 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0007 | 0/0 | 407 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0008 | 0/0 | 378 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0009 | 0/0 | 407 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0010 | 0/0 | 407 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1224 | 226 | 34 | 43 | 118 | 5 | 24 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
c0002 | 0/0 | 1224 | 55 | 24 | 7 | 21 | 0 | 3 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
c0003 | 0/0 | 1224 | 25 | 10 | 9 | 0 | 3 | 3 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
c0004 | 0/0 | 1224 | 5 | 5 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
c0005 | 0/0 | 1224 | 4 | 4 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
c0006 | 0/0 | 1224 | 4 | 0 | 0 | 4 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
c0007 | 0/0 | 1267 | 3 | 3 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
c0008 | 0/0 | 1224 | 3 | 3 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
c0009 | 0/0 | 1224 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
c0010 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
c0011 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
c0012 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
c0013 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
c0014 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
c0015 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 8545 | 79 | 17 | 24 | 29 | 1 | 8 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0002 | 0/0 | 8545 | 31 | 0 | 0 | 31 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0003 | 0/0 | 8544 | 25 | 2 | 4 | 16 | 0 | 3 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0004 | 0/0 | 8545 | 21 | 1 | 2 | 17 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0005 | 0/0 | 8546 | 10 | 4 | 4 | 0 | 1 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0006 | 0/0 | 8545 | 9 | 0 | 0 | 9 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0007 | 0/0 | 8545 | 8 | 0 | 1 | 5 | 0 | 2 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0008 | 0/0 | 8546 | 7 | 2 | 3 | 1 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0009 | 0/0 | 8542 | 7 | 0 | 0 | 7 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0010 | 0/0 | 8546 | 6 | 0 | 2 | 2 | 0 | 2 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0011 | 0/0 | 8545 | 6 | 0 | 5 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0012 | 0/0 | 8547 | 5 | 5 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0013 | 0/0 | 8544 | 4 | 4 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0014 | 0/1 | 8546 | 4 | 0 | 2 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0015 | 0/0 | 8544 | 4 | 4 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0016 | 0/0 | 8545 | 3 | 0 | 0 | 3 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0017 | 0/0 | 8545 | 3 | 0 | 0 | 0 | 0 | 3 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0018 | 0/0 | 8545 | 3 | 3 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0019 | 0/0 | 8547 | 3 | 1 | 1 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0020 | 0/0 | 8544 | 3 | 0 | 0 | 2 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0021 | 0/0 | 8546 | 3 | 3 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0022 | 0/0 | 8546 | 3 | 3 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0023 | 0/0 | 8546 | 2 | 0 | 0 | 2 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0024 | 0/0 | 8545 | 2 | 2 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0025 | 0/0 | 8548 | 2 | 0 | 1 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0026 | 0/0 | 8544 | 2 | 0 | 0 | 2 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0027 | 0/0 | 8545 | 2 | 2 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0028 | 0/0 | 8545 | 2 | 0 | 0 | 1 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0029 | 0/0 | 8546 | 2 | 0 | 1 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0030 | 0/0 | 8544 | 2 | 0 | 0 | 1 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0031 | 0/0 | 8545 | 2 | 2 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0032 | 1/0 | 8547 | 2 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0033 | 0/0 | 8545 | 2 | 2 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0034 | 0/0 | 8545 | 2 | 2 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0035 | 0/0 | 8545 | 2 | 2 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0036 | 0/0 | 8545 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0037 | 0/0 | 8543 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0038 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0039 | 0/0 | 8547 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0040 | 0/0 | 8546 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0041 | 0/0 | 8545 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0042 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0043 | 0/0 | 8547 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0044 | 0/0 | 8548 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0045 | 0/0 | 8545 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0046 | 0/0 | 8545 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0047 | 0/0 | 8546 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0048 | 0/0 | 8546 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0049 | 0/0 | 8546 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0050 | 0/0 | 8546 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0051 | 0/0 | 8546 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0052 | 0/0 | 8546 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0053 | 0/0 | 8548 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0054 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0055 | 0/0 | 8547 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0056 | 0/0 | 8547 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0057 | 0/0 | 8547 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0058 | 0/0 | 8546 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0059 | 0/0 | 8546 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0060 | 0/0 | 8545 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0061 | 0/0 | 8545 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0062 | 0/0 | 8545 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0063 | 0/0 | 8555 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0064 | 0/0 | 8545 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0065 | 0/0 | 8545 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0066 | 0/0 | 8545 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0067 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0068 | 0/0 | 8545 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0069 | 0/0 | 8547 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0070 | 0/0 | 8546 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0071 | 0/0 | 8546 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0072 | 0/0 | 8546 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0073 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0074 | 0/0 | 8543 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0075 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0076 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0077 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0078 | 0/0 | 8543 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0079 | 0/0 | 8546 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0080 | 0/0 | 8546 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0081 | 0/0 | 8545 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0082 | 0/0 | 8545 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0083 | 0/0 | 8546 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0084 | 0/0 | 8545 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0085 | 0/0 | 8547 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0086 | 0/0 | 8547 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0087 | 0/0 | 8547 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0088 | 0/0 | 8547 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0089 | 0/0 | 8547 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0090 | 0/0 | 8546 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0091 | 0/0 | 8547 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0092 | 0/0 | 8545 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0093 | 0/0 | 8545 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
t0094 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1224 | 226 | 34 | 43 | 118 | 5 | 24 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002 | 0/0 | 1224 | 55 | 24 | 7 | 21 | 0 | 3 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0003 | 0/0 | 1224 | 25 | 10 | 9 | 0 | 3 | 3 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0005 | 0/0 | 1224 | 4 | 4 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0002c0004 | 0/0 | 1224 | 5 | 5 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0002c0009 | 0/0 | 1224 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0002c0014 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0003c0006 | 0/0 | 1224 | 4 | 0 | 0 | 4 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0004c0008 | 0/0 | 1224 | 3 | 3 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0005c0007 | 0/0 | 1267 | 3 | 3 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0006c0015 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0007c0013 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0008c0010 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0009c0011 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0010c0012 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9768 | 59 | 9 | 22 | 20 | 1 | 7 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0002 | 0/0 | 9768 | 28 | 0 | 0 | 28 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0003 | 0/0 | 9767 | 25 | 2 | 4 | 16 | 0 | 3 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0004 | 0/0 | 9768 | 20 | 1 | 2 | 16 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0006 | 0/0 | 9768 | 9 | 0 | 0 | 9 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0008 | 0/0 | 9769 | 4 | 1 | 1 | 1 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0010 | 0/0 | 9769 | 6 | 0 | 2 | 2 | 0 | 2 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0011 | 0/0 | 9768 | 6 | 0 | 5 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0012 | 0/0 | 9770 | 5 | 5 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0013 | 0/0 | 9767 | 4 | 4 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0014 | 0/1 | 9769 | 4 | 0 | 2 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0016 | 0/0 | 9768 | 3 | 0 | 0 | 3 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0017 | 0/0 | 9768 | 3 | 0 | 0 | 0 | 0 | 3 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0020 | 0/0 | 9767 | 3 | 0 | 0 | 2 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0023 | 0/0 | 9769 | 2 | 0 | 0 | 2 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0024 | 0/0 | 9768 | 2 | 2 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0026 | 0/0 | 9767 | 2 | 0 | 0 | 2 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0028 | 0/0 | 9768 | 2 | 0 | 0 | 1 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0029 | 0/0 | 9769 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0030 | 0/0 | 9767 | 2 | 0 | 0 | 1 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0032 | 1/0 | 9770 | 1 | 0 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0036 | 0/0 | 9768 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0037 | 0/0 | 9766 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0038 | 0/0 | 9767 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0039 | 0/0 | 9770 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0040 | 0/0 | 9769 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0041 | 0/0 | 9768 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0042 | 0/0 | 9767 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0043 | 0/0 | 9770 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0044 | 0/0 | 9771 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0045 | 0/0 | 9768 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0047 | 0/0 | 9769 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0050 | 0/0 | 9769 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0051 | 0/0 | 9769 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0052 | 0/0 | 9769 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0053 | 0/0 | 9771 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0059 | 0/0 | 9769 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0060 | 0/0 | 9768 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0062 | 0/0 | 9768 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0063 | 0/0 | 9778 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0064 | 0/0 | 9768 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0065 | 0/0 | 9768 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0067 | 0/0 | 9767 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0068 | 0/0 | 9768 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0069 | 0/0 | 9770 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0071 | 0/0 | 9769 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0073 | 0/0 | 9767 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0074 | 0/0 | 9766 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0075 | 0/0 | 9767 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0076 | 0/0 | 9767 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0077 | 0/0 | 9767 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0078 | 0/0 | 9766 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0079 | 0/0 | 9769 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0080 | 0/0 | 9769 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0081 | 0/0 | 9768 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0001t0084 | 0/0 | 9768 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0001 | 0/0 | 9768 | 13 | 5 | 2 | 5 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0002 | 0/0 | 9768 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0007 | 0/0 | 9768 | 8 | 0 | 1 | 5 | 0 | 2 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0008 | 0/0 | 9769 | 3 | 1 | 2 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0009 | 0/0 | 9765 | 7 | 0 | 0 | 7 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0022 | 0/0 | 9769 | 3 | 3 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0027 | 0/0 | 9768 | 2 | 2 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0029 | 0/0 | 9769 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0033 | 0/0 | 9768 | 2 | 2 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0035 | 0/0 | 9768 | 2 | 2 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0048 | 0/0 | 9769 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0049 | 0/0 | 9769 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0054 | 0/0 | 9771 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0057 | 0/0 | 9770 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0061 | 0/0 | 9768 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0072 | 0/0 | 9769 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0087 | 0/0 | 9770 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0089 | 0/0 | 9770 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0090 | 0/0 | 9769 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0091 | 0/0 | 9770 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0092 | 0/0 | 9768 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0093 | 0/0 | 9768 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0002t0094 | 0/0 | 9767 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0003t0005 | 0/0 | 9769 | 9 | 3 | 4 | 0 | 1 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0003t0019 | 0/0 | 9770 | 3 | 1 | 1 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0003t0021 | 0/0 | 9769 | 3 | 3 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0003t0025 | 0/0 | 9771 | 2 | 0 | 1 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0003t0055 | 0/0 | 9770 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0003t0056 | 0/0 | 9770 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0003t0058 | 0/0 | 9769 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0003t0070 | 0/0 | 9769 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0003t0083 | 0/0 | 9769 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0003t0085 | 0/0 | 9770 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0003t0086 | 0/0 | 9770 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0003t0088 | 0/0 | 9770 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0001c0005t0015 | 0/0 | 9767 | 4 | 4 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0002c0004t0018 | 0/0 | 9768 | 3 | 3 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0002c0004t0034 | 0/0 | 9768 | 2 | 2 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0002c0009t0066 | 0/0 | 9768 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0002c0014t0046 | 0/0 | 9768 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0003c0006t0001 | 0/0 | 9768 | 4 | 0 | 0 | 4 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0004c0008t0001 | 0/0 | 9768 | 3 | 3 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0005c0007t0005 | 0/0 | 9812 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0005c0007t0031 | 0/0 | 9811 | 2 | 2 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0006c0015t0002 | 0/0 | 9768 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0007c0013t0082 | 0/0 | 9768 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0008c0010t0032 | 0/0 | 9770 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0009c0011t0004 | 0/0 | 9768 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
a0010c0012t0002 | 0/0 | 9768 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | copy fasta | chr2 | 171310746 | 171438990 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0008g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0008g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0010g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0010g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0010g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0010g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0010g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0010g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0011g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0011g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0011g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0011g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0011g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0011g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0012g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0012g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0012g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0012g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0012g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0013g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0013g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0013g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0014g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0014g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0014g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0014g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0016g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0016g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0016g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0017g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0017g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0017g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0020g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0020g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0020g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0023g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0023g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0024g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0024g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0026g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0026g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0028g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0028g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0029g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0030g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0030g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0032g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0036g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0037g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0038g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0039g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0040g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0041g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0042g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0043g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0044g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0045g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0047g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0050g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0051g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0052g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0053g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0059g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0060g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0062g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0063g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0064g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0065g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0067g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0068g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0069g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0071g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0073g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0074g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0075g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0076g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0077g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0078g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0079g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0080g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0081g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0001t0084g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0007g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0007g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0007g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0007g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0007g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0007g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0007g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0007g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0008g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0008g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0008g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0009g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0009g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0009g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0009g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0009g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0009g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0009g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0022g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0022g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0022g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0027g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0027g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0029g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0033g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0033g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0035g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0035g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0048g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0049g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0054g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0057g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0061g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0072g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0087g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0089g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0090g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0091g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0092g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0093g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0002t0094g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0005g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0005g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0005g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0019g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0019g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0019g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0021g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0021g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0021g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0025g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0025g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0055g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0056g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0058g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0070g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0083g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0085g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0086g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0003t0088g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0005t0015g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0005t0015g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0005t0015g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0001c0005t0015g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0002c0004t0018g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0002c0004t0018g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0002c0004t0018g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0002c0004t0034g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0002c0004t0034g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0002c0009t0066g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0002c0014t0046g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0003c0006t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0003c0006t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0003c0006t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0003c0006t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0004c0008t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0004c0008t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0004c0008t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0005c0007t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0005c0007t0031g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0005c0007t0031g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0006c0015t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0007c0013t0082g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0008c0010t0032g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0009c0011t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
a0010c0012t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0003 | t0025 | g0030 | EUR | FIN | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00280 | hp2 | a0001 | c0001 | t0020 | g0112 | EUR | FIN | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00408 | hp1 | a0001 | c0002 | t0009 | g0290 | EAS | CHS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | CHS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00423 | hp1 | a0001 | c0001 | t0062 | g0045 | EAS | CHS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00423 | hp2 | a0001 | c0002 | t0048 | g0312 | EAS | CHS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00558 | hp1 | a0001 | c0001 | t0045 | g0241 | EAS | CHS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00597 | hp1 | a0001 | c0002 | t0009 | g0270 | EAS | CHS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | CHS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00621 | hp1 | a0001 | c0001 | t0047 | g0166 | EAS | CHS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00621 | hp2 | a0001 | c0001 | t0028 | g0231 | EAS | CHS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00642 | hp1 | a0001 | c0003 | t0005 | g0106 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00738 | hp1 | a0001 | c0003 | t0086 | g0028 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01074 | hp1 | a0002 | c0009 | t0066 | g0091 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01081 | hp1 | a0001 | c0002 | t0007 | g0308 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01106 | hp1 | a0001 | c0001 | t0064 | g0210 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01106 | hp2 | a0001 | c0003 | t0025 | g0031 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01109 | hp1 | a0001 | c0002 | t0029 | g0056 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01109 | hp2 | a0001 | c0001 | t0069 | g0248 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01168 | hp1 | a0001 | c0002 | t0008 | g0223 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01169 | hp2 | a0001 | c0002 | t0008 | g0217 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01175 | hp1 | a0001 | c0001 | t0008 | g0234 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0280 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01192 | hp2 | a0001 | c0001 | t0014 | g0131 | AMR | PUR | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01255 | hp1 | a0001 | c0001 | t0014 | g0137 | AMR | CLM | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0281 | AMR | CLM | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01256 | hp1 | a0001 | c0003 | t0005 | g0105 | AMR | CLM | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01258 | hp1 | a0001 | c0001 | t0010 | g0285 | AMR | CLM | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01258 | hp2 | a0001 | c0001 | t0081 | g0136 | AMR | CLM | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01261 | hp1 | a0001 | c0002 | t0092 | g0321 | AMR | CLM | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01261 | hp2 | a0001 | c0001 | t0071 | g0088 | AMR | CLM | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01346 | hp1 | a0001 | c0003 | t0019 | g0027 | AMR | CLM | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | CLM | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01433 | hp2 | a0001 | c0001 | t0010 | g0286 | AMR | CLM | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01496 | hp2 | a0001 | c0003 | t0005 | g0029 | AMR | CLM | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01515 | hp1 | a0001 | c0003 | t0070 | g0033 | EUR | IBS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01515 | hp2 | a0001 | c0001 | t0063 | g0139 | EUR | IBS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01517 | hp1 | a0001 | c0001 | t0060 | g0097 | EUR | IBS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01884 | hp1 | a0007 | c0013 | t0082 | g0297 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01884 | hp2 | a0001 | c0002 | t0027 | g0304 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01891 | hp1 | a0001 | c0001 | t0052 | g0071 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01891 | hp2 | a0001 | c0002 | t0008 | g0228 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01934 | hp2 | a0001 | c0001 | t0011 | g0202 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01952 | hp1 | a0001 | c0001 | t0011 | g0255 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01975 | hp2 | a0001 | c0001 | t0011 | g0260 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01978 | hp1 | a0001 | c0001 | t0053 | g0244 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01978 | hp2 | a0001 | c0003 | t0056 | g0253 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01981 | hp2 | a0001 | c0003 | t0005 | g0107 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02004 | hp2 | a0001 | c0001 | t0011 | g0258 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02015 | hp1 | a0001 | c0001 | t0050 | g0208 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02015 | hp2 | a0006 | c0015 | t0002 | g0190 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02027 | hp1 | a0001 | c0001 | t0023 | g0013 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02027 | hp2 | a0001 | c0002 | t0007 | g0310 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02040 | hp1 | a0001 | c0002 | t0009 | g0292 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02055 | hp1 | a0001 | c0002 | t0054 | g0016 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02055 | hp2 | a0001 | c0005 | t0015 | g0101 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02056 | hp2 | a0001 | c0001 | t0023 | g0179 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02080 | hp1 | a0001 | c0002 | t0049 | g0311 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02129 | hp1 | a0001 | c0001 | t0006 | g0181 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02129 | hp2 | a0001 | c0002 | t0061 | g0314 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02132 | hp1 | a0001 | c0001 | t0059 | g0188 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02132 | hp2 | a0001 | c0002 | t0007 | g0306 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02135 | hp2 | a0001 | c0001 | t0010 | g0287 | EAS | KHV | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02145 | hp1 | a0001 | c0001 | t0012 | g0051 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02145 | hp2 | a0001 | c0001 | t0008 | g0169 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | CDX | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | CDX | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02258 | hp1 | a0001 | c0003 | t0021 | g0239 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0227 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02280 | hp1 | a0005 | c0007 | t0005 | g0235 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02280 | hp2 | a0002 | c0004 | t0018 | g0073 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02293 | hp2 | a0001 | c0001 | t0011 | g0266 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02300 | hp2 | a0001 | c0003 | t0083 | g0032 | AMR | PEL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02451 | hp1 | a0001 | c0001 | t0078 | g0294 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0222 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02572 | hp1 | a0002 | c0014 | t0046 | g0089 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02572 | hp2 | a0001 | c0003 | t0005 | g0021 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0242 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02602 | hp2 | a0001 | c0001 | t0017 | g0204 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02615 | hp2 | a0001 | c0001 | t0013 | g0007 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02622 | hp1 | a0001 | c0001 | t0012 | g0049 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02647 | hp1 | a0005 | c0007 | t0031 | g0020 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02647 | hp2 | a0001 | c0002 | t0022 | g0317 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02717 | hp1 | a0001 | c0003 | t0055 | g0015 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02717 | hp2 | a0002 | c0004 | t0018 | g0092 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02735 | hp2 | a0001 | c0003 | t0005 | g0034 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02809 | hp1 | a0001 | c0005 | t0015 | g0100 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02818 | hp2 | a0004 | c0008 | t0001 | g0300 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02886 | hp2 | a0001 | c0001 | t0077 | g0116 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02895 | hp2 | a0001 | c0002 | t0089 | g0325 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02896 | hp1 | a0001 | c0001 | t0039 | g0004 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02896 | hp2 | a0001 | c0002 | t0022 | g0318 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02897 | hp2 | a0001 | c0002 | t0022 | g0320 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02922 | hp1 | a0001 | c0001 | t0013 | g0008 | AFR | ESN | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02922 | hp2 | a0001 | c0003 | t0005 | g0023 | AFR | ESN | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02965 | hp1 | a0001 | c0001 | t0037 | g0005 | AFR | ESN | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02965 | hp2 | a0001 | c0005 | t0015 | g0103 | AFR | ESN | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02970 | hp1 | a0001 | c0005 | t0015 | g0099 | AFR | ESN | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02970 | hp2 | a0002 | c0004 | t0034 | g0329 | AFR | ESN | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02976 | hp1 | a0001 | c0001 | t0024 | g0207 | AFR | ESN | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02976 | hp2 | a0001 | c0002 | t0033 | g0324 | AFR | ESN | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03041 | hp1 | a0001 | c0001 | t0013 | g0010 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03041 | hp2 | a0001 | c0001 | t0074 | g0090 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03098 | hp1 | a0001 | c0002 | t0057 | g0220 | AFR | MSL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03098 | hp2 | a0001 | c0003 | t0019 | g0019 | AFR | MSL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03139 | hp1 | a0004 | c0008 | t0001 | g0299 | AFR | ESN | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03139 | hp2 | a0001 | c0002 | t0027 | g0305 | AFR | ESN | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03195 | hp2 | a0001 | c0001 | t0012 | g0050 | AFR | ESN | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03209 | hp1 | a0001 | c0002 | t0090 | g0323 | AFR | MSL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03209 | hp2 | a0001 | c0003 | t0005 | g0022 | AFR | MSL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03225 | hp1 | a0002 | c0004 | t0018 | g0072 | AFR | MSL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03225 | hp2 | a0001 | c0001 | t0012 | g0236 | AFR | MSL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03239 | hp1 | a0001 | c0001 | t0065 | g0134 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03239 | hp2 | a0001 | c0001 | t0010 | g0265 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03453 | hp1 | a0001 | c0003 | t0088 | g0014 | AFR | MSL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0229 | AFR | MSL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03486 | hp1 | a0001 | c0002 | t0087 | g0219 | AFR | MSL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03486 | hp2 | a0001 | c0002 | t0091 | g0316 | AFR | MSL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03490 | hp2 | a0001 | c0001 | t0017 | g0212 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03492 | hp1 | a0001 | c0001 | t0051 | g0211 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03540 | hp1 | a0005 | c0007 | t0031 | g0018 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03540 | hp2 | a0001 | c0002 | t0035 | g0327 | AFR | GWD | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03654 | hp1 | a0001 | c0002 | t0007 | g0307 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0108 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0121 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0127 | SAS | STU | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03688 | hp2 | a0001 | c0001 | t0030 | g0254 | SAS | STU | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03704 | hp1 | a0001 | c0002 | t0007 | g0309 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0054 | SAS | BEB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03831 | hp2 | a0001 | c0003 | t0058 | g0104 | SAS | BEB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03834 | hp2 | a0001 | c0001 | t0029 | g0252 | SAS | BEB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03942 | hp1 | a0001 | c0001 | t0008 | g0047 | SAS | BEB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03942 | hp2 | a0001 | c0001 | t0017 | g0053 | SAS | BEB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG04184 | hp2 | a0001 | c0001 | t0028 | g0113 | SAS | BEB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG04199 | hp1 | a0001 | c0001 | t0010 | g0257 | SAS | STU | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG04199 | hp2 | a0001 | c0003 | t0019 | g0024 | SAS | STU | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG04228 | hp1 | a0001 | c0001 | t0014 | g0209 | SAS | STU | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG04228 | hp2 | a0001 | c0001 | t0084 | g0247 | SAS | STU | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | CHB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18906 | hp1 | a0002 | c0004 | t0034 | g0328 | AFR | YRI | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18906 | hp2 | a0001 | c0001 | t0041 | g0194 | AFR | YRI | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18941 | hp2 | a0001 | c0002 | t0007 | g0298 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18942 | hp1 | a0001 | c0002 | t0009 | g0291 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18942 | hp2 | a0001 | c0001 | t0026 | g0150 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18944 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18947 | hp1 | a0003 | c0006 | t0001 | g0129 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18947 | hp2 | a0001 | c0001 | t0075 | g0078 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18951 | hp1 | a0010 | c0012 | t0002 | g0167 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18952 | hp1 | a0001 | c0001 | t0020 | g0274 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18952 | hp2 | a0001 | c0001 | t0073 | g0063 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18953 | hp1 | a0001 | c0001 | t0016 | g0061 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18953 | hp2 | a0001 | c0001 | t0006 | g0193 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18962 | hp1 | a0001 | c0001 | t0080 | g0284 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18962 | hp2 | a0001 | c0001 | t0026 | g0149 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18963 | hp1 | a0001 | c0001 | t0006 | g0191 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18964 | hp2 | a0001 | c0001 | t0043 | g0171 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18969 | hp1 | a0001 | c0001 | t0006 | g0163 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18969 | hp2 | a0001 | c0002 | t0007 | g0303 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18971 | hp1 | a0003 | c0006 | t0001 | g0153 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18973 | hp1 | a0003 | c0006 | t0001 | g0130 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18975 | hp2 | a0001 | c0002 | t0009 | g0269 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18979 | hp2 | a0001 | c0001 | t0006 | g0199 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18982 | hp1 | a0001 | c0001 | t0020 | g0069 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18982 | hp2 | a0001 | c0001 | t0011 | g0259 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18984 | hp2 | a0001 | c0001 | t0067 | g0243 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18985 | hp2 | a0001 | c0001 | t0008 | g0046 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18987 | hp2 | a0001 | c0001 | t0079 | g0261 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18990 | hp1 | a0001 | c0001 | t0006 | g0165 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18992 | hp2 | a0003 | c0006 | t0001 | g0152 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19000 | hp1 | a0001 | c0002 | t0009 | g0249 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19001 | hp1 | a0001 | c0001 | t0044 | g0162 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19005 | hp2 | a0001 | c0002 | t0007 | g0313 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19006 | hp1 | a0001 | c0002 | t0002 | g0302 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19009 | hp1 | a0001 | c0001 | t0010 | g0245 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19010 | hp2 | a0001 | c0001 | t0016 | g0064 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19011 | hp2 | a0001 | c0001 | t0076 | g0074 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19030 | hp1 | a0001 | c0001 | t0040 | g0198 | AFR | LWK | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19030 | hp2 | a0001 | c0003 | t0021 | g0240 | AFR | LWK | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19043 | hp1 | a0008 | c0010 | t0032 | g0052 | AFR | LWK | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19043 | hp2 | a0001 | c0001 | t0012 | g0123 | AFR | LWK | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19054 | hp2 | a0001 | c0001 | t0030 | g0277 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19060 | hp2 | a0009 | c0011 | t0004 | g0196 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19063 | hp2 | a0001 | c0002 | t0009 | g0293 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19064 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19068 | hp1 | a0001 | c0001 | t0006 | g0200 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19080 | hp2 | a0001 | c0001 | t0042 | g0077 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19240 | hp1 | a0001 | c0002 | t0093 | g0322 | AFR | YRI | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA19240 | hp2 | a0001 | c0003 | t0085 | g0238 | AFR | YRI | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA20129 | hp1 | a0001 | c0002 | t0033 | g0330 | AFR | ASW | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ASW | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA20752 | hp1 | a0001 | c0001 | t0068 | g0026 | EUR | TSI | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA20752 | hp2 | a0001 | c0003 | t0005 | g0025 | EUR | TSI | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0295 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02486 | hp1 | a0001 | c0001 | t0036 | g0003 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0221 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02559 | hp1 | a0001 | c0001 | t0038 | g0006 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG02559 | hp2 | a0001 | c0003 | t0021 | g0237 | AFR | ACB | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG03471 | hp2 | a0001 | c0002 | t0094 | g0319 | AFR | MSL | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG06807 | hp1 | a0001 | c0001 | t0024 | g0102 | AFR | USA | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0279 | AFR | USA | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18955 | hp1 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA18955 | hp2 | a0001 | c0001 | t0016 | g0062 | EAS | JPT | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA20300 | hp1 | a0001 | c0002 | t0035 | g0326 | AFR | USA | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA20300 | hp2 | a0001 | c0002 | t0072 | g0017 | AFR | USA | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA21309 | hp1 | a0001 | c0001 | t0013 | g0009 | AFR | LWK | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
NA21309 | hp2 | a0004 | c0008 | t0001 | g0301 | AFR | LWK | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0014 | g0216 | REF | REF | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0032 | g0124 | REF | REF | METTL8_chr2_171310746_171438990 | METTL8 | chr2 | 171310746 | 171438990 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:171324261
|
G | A | 1 | a0008 | 1 | NA19043.hp1 | stop_gained | HIGH | c.1135C>T | p.Arg379* | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1255/9770 | 1135/1224 | 379/407 | chr2 | 171324261 | ||
chr2:171324264
|
G | A | 1 | a0009 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.1132C>T | p.His378Tyr | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1252/9770 | 1132/1224 | 378/407 | chr2 | 171324264 | ||
chr2:171324321
|
T | C | 1 | a0002 | 7 | HG01074.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
missense_variant | MODERATE | c.1075A>G | p.Lys359Glu | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1195/9770 | 1075/1224 | 359/407 | chr2 | 171324321 | ||
chr2:171324332
|
C | T | 1 | a0003 | 4 | NA18947.hp1 NA18971.hp1 NA18973.hp1 others(1): Show |
missense_variant | MODERATE | c.1064G>A | p.Ser355Asn | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1184/9770 | 1064/1224 | 355/407 | chr2 | 171324332 | ||
chr2:171325903
|
T | C | 1 | a0010 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.971A>G | p.His324Arg | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/10 | 1091/9770 | 971/1224 | 324/407 | chr2 | 171325903 | ||
chr2:171326140
|
C | CCTTGCAT others(36): Show |
1 | a0005 | 3 | HG02280.hp1 HG02647.hp1 HG03540.hp1 |
frameshift_variant | HIGH | c.861-35_868dupAAACT others(38): Show |
p.Gly290fs | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 8/10 | 988/9770 | 868/1224 | 290/407 | chr2 | 171326140 | ||
chr2:171330620
|
G | C | 1 | a0007 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.799C>G | p.Pro267Ala | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/10 | 919/9770 | 799/1224 | 267/407 | chr2 | 171330620 | ||
chr2:171339365
|
G | A | 1 | a0004 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.425C>T | p.Ser142Leu | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/10 | 545/9770 | 425/1224 | 142/407 | chr2 | 171339365 | ||
chr2:171392124
|
T | C | 1 | a0006 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.62A>G | p.Tyr21Cys | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/10 | 182/9770 | 62/1224 | 21/407 | chr2 | 171392124 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:171331810
|
G | A | 2 | a0002c0004a0002c0014 | 6 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(3): Show |
synonymous_variant | LOW | c.714C>T | p.Leu238Leu | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 6/10 | 834/9770 | 714/1224 | 238/407 | chr2 | 171331810 | ||
chr2:171331828
|
A | C | 2 | a0001c0005a0002c0009 | 5 | HG01074.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
synonymous_variant | LOW | c.696T>G | p.Ala232Ala | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 6/10 | 816/9770 | 696/1224 | 232/407 | chr2 | 171331828 | ||
chr2:171331858
|
C | T | 1 | a0001c0003 | 25 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(22): Show |
synonymous_variant | LOW | c.666G>A | p.Pro222Pro | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 6/10 | 786/9770 | 666/1224 | 222/407 | chr2 | 171331858 | ||
chr2:171360459
|
T | C | 5 | a0001c0002a0001c0003a0002c0004others(2): Show | 91 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(88): Show |
synonymous_variant | LOW | c.198A>G | p.Lys66Lys | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/10 | 318/9770 | 198/1224 | 66/407 | chr2 | 171360459 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:171315843
|
T | C | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8329A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8329 | chr2 | 171315843 | |||||
chr2:171315844
|
A | G | 1 | a0001c0001t0047 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8328T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8328 | chr2 | 171315844 | |||||
chr2:171315856
|
A | G | 17 | a0001c0001t0029a0001c0002t0022a0001c0002t0029others(14): Show | 32 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*8316T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8316 | chr2 | 171315856 | |||||
chr2:171315864
|
T | A | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8308A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8308 | chr2 | 171315864 | |||||
chr2:171315869
|
T | A | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8303A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8303 | chr2 | 171315869 | |||||
chr2:171315871
|
G | A | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8301C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8301 | chr2 | 171315871 | |||||
chr2:171315873
|
G | A | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8299C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8299 | chr2 | 171315873 | |||||
chr2:171315874
|
A | T | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8298T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8298 | chr2 | 171315874 | |||||
chr2:171315880
|
G | A | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8292C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8292 | chr2 | 171315880 | |||||
chr2:171315881
|
G | C | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8291C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8291 | chr2 | 171315881 | |||||
chr2:171315882
|
G | C | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8290C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8290 | chr2 | 171315882 | |||||
chr2:171315887
|
T | TAATATAC others(3): Show |
1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8284_*8285insGATG others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8284 | chr2 | 171315887 | |||||
chr2:171315895
|
G | C | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8277C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8277 | chr2 | 171315895 | |||||
chr2:171315897
|
G | A | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8275C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8275 | chr2 | 171315897 | |||||
chr2:171315898
|
G | A | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8274C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8274 | chr2 | 171315898 | |||||
chr2:171315902
|
C | T | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8270G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8270 | chr2 | 171315902 | |||||
chr2:171315905
|
A | T | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8267T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8267 | chr2 | 171315905 | |||||
chr2:171315911
|
A | C | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8261T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8261 | chr2 | 171315911 | |||||
chr2:171315918
|
C | G | 1 | a0001c0001t0063 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8254G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8254 | chr2 | 171315918 | |||||
chr2:171316025
|
A | C | 1 | a0001c0001t0084 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8147T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 8147 | chr2 | 171316025 | |||||
chr2:171316235
|
G | C | 1 | a0001c0001t0077 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7937C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 7937 | chr2 | 171316235 | |||||
chr2:171316354
|
G | A | 81 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(78): Show | 288 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*7818C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 7818 | chr2 | 171316354 | |||||
chr2:171316495
|
A | G | 4 | a0001c0002t0072a0001c0002t0087a0001c0003t0088others(1): Show | 5 | HG02647.hp1 HG03453.hp1 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7677T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 7677 | chr2 | 171316495 | |||||
chr2:171316599
|
T | A | 2 | a0001c0001t0016a0001c0001t0073 | 4 | NA18952.hp2 NA18953.hp1 NA18955.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7573A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 7573 | chr2 | 171316599 | |||||
chr2:171316737
|
C | A | 1 | a0001c0001t0050 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7435G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 7435 | chr2 | 171316737 | |||||
chr2:171316859
|
G | T | 1 | a0001c0002t0009 | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7313C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 7313 | chr2 | 171316859 | |||||
chr2:171316860
|
C | T | 2 | a0001c0001t0053a0001c0001t0069 | 2 | HG01109.hp2 HG01978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7312G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 7312 | chr2 | 171316860 | |||||
chr2:171316990
|
A | G | 1 | a0001c0002t0061 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7182T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 7182 | chr2 | 171316990 | |||||
chr2:171317091
|
A | C | 1 | a0001c0002t0091 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7081T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 7081 | chr2 | 171317091 | |||||
chr2:171317099
|
C | T | 2 | a0001c0002t0022a0001c0003t0055 | 4 | HG02647.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7073G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 7073 | chr2 | 171317099 | |||||
chr2:171317433
|
G | A | 1 | a0001c0001t0064 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6739C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 6739 | chr2 | 171317433 | |||||
chr2:171317640
|
A | G | 85 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(82): Show | 293 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*6532T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 6532 | chr2 | 171317640 | |||||
chr2:171317641
|
A | C | 85 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(82): Show | 293 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*6531T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 6531 | chr2 | 171317641 | |||||
chr2:171317672
|
G | A | 2 | a0001c0001t0017a0001c0001t0051 | 4 | HG02602.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6500C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 6500 | chr2 | 171317672 | |||||
chr2:171317684
|
C | T | 1 | a0001c0002t0009 | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6488G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 6488 | chr2 | 171317684 | |||||
chr2:171317753
|
T | C | 85 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(82): Show | 293 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*6419A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 6419 | chr2 | 171317753 | |||||
chr2:171318012
|
C | G | 1 | a0001c0001t0062 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6160G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 6160 | chr2 | 171318012 | |||||
chr2:171318249
|
A | G | 1 | a0001c0001t0076 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5923T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 5923 | chr2 | 171318249 | |||||
chr2:171318273
|
C | T | 2 | a0002c0004t0018a0002c0004t0034 | 5 | HG02280.hp2 HG02717.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5899G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 5899 | chr2 | 171318273 | |||||
chr2:171318558
|
G | A | 80 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(77): Show | 281 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*5614C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 5614 | chr2 | 171318558 | |||||
chr2:171318679
|
A | G | 1 | a0001c0003t0070 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5493T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 5493 | chr2 | 171318679 | |||||
chr2:171318737
|
T | C | 2 | a0001c0002t0072a0005c0007t0031 | 3 | HG02647.hp1 HG03540.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5435A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 5435 | chr2 | 171318737 | |||||
chr2:171318948
|
G | T | 11 | a0001c0001t0074a0001c0002t0007a0001c0002t0027others(8): Show | 20 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*5224C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 5224 | chr2 | 171318948 | |||||
chr2:171319026
|
C | G | 2 | a0001c0002t0087a0001c0003t0088 | 2 | HG03453.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5146G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 5146 | chr2 | 171319026 | |||||
chr2:171319254
|
G | A | 1 | a0001c0001t0065 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4918C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 4918 | chr2 | 171319254 | |||||
chr2:171319438
|
A | T | 2 | a0001c0003t0021a0001c0003t0085 | 4 | HG02258.hp1 HG02559.hp2 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4734T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 4734 | chr2 | 171319438 | |||||
chr2:171319455
|
G | T | 1 | a0001c0001t0080 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4717C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 4717 | chr2 | 171319455 | |||||
chr2:171319459
|
T | C | 1 | a0001c0002t0093 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4713A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 4713 | chr2 | 171319459 | |||||
chr2:171319467
|
A | G | 12 | a0001c0001t0074a0001c0002t0007a0001c0002t0027others(9): Show | 21 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4705T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 4705 | chr2 | 171319467 | |||||
chr2:171319470
|
A | C | 1 | a0001c0002t0022 | 3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4702T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 4702 | chr2 | 171319470 | |||||
chr2:171319546
|
C | T | 1 | a0001c0002t0092 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4626G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 4626 | chr2 | 171319546 | |||||
chr2:171319676
|
G | A | 1 | a0001c0001t0043 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4496C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 4496 | chr2 | 171319676 | |||||
chr2:171320658
|
A | C | 2 | a0001c0001t0011a0001c0001t0079 | 7 | HG01934.hp2 HG01952.hp1 HG01975.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3514T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 3514 | chr2 | 171320658 | |||||
chr2:171320728
|
G | A | 1 | a0001c0001t0037 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3444C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 3444 | chr2 | 171320728 | |||||
chr2:171320982
|
C | T | 2 | a0001c0002t0087a0001c0003t0088 | 2 | HG03453.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3190G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 3190 | chr2 | 171320982 | |||||
chr2:171321009
|
T | C | 5 | a0001c0001t0024a0001c0005t0015a0002c0004t0018others(2): Show | 12 | HG01074.hp1 HG02055.hp2 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3163A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 3163 | chr2 | 171321009 | |||||
chr2:171321048
|
G | A | 1 | a0001c0001t0041 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3124C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 3124 | chr2 | 171321048 | |||||
chr2:171321175
|
A | G | 1 | a0001c0001t0060 | 1 | HG01517.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2997T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 2997 | chr2 | 171321175 | |||||
chr2:171321962
|
A | AT | 12 | a0001c0001t0004a0001c0001t0010a0001c0001t0011others(9): Show | 41 | HG01109.hp2 HG01175.hp2 HG01255.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2209dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 2209 | chr2 | 171321962 | |||||
chr2:171321962
|
AT | A | 8 | a0001c0001t0037a0001c0001t0067a0001c0001t0074others(5): Show | 15 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2209delA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 2209 | chr2 | 171321962 | |||||
chr2:171321963
|
T | A | 1 | a0001c0002t0035 | 2 | HG03540.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2209A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 2209 | chr2 | 171321963 | |||||
chr2:171322056
|
G | A | 1 | a0001c0001t0038 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2116C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 2116 | chr2 | 171322056 | |||||
chr2:171322120
|
G | A | 3 | a0001c0001t0012a0001c0002t0087a0001c0003t0088 | 7 | HG02145.hp1 HG02622.hp1 HG03195.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2052C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 2052 | chr2 | 171322120 | |||||
chr2:171322193
|
T | G | 1 | a0001c0001t0068 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1979A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1979 | chr2 | 171322193 | |||||
chr2:171322254
|
C | T | 1 | a0001c0001t0075 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1918G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1918 | chr2 | 171322254 | |||||
chr2:171322307
|
C | T | 1 | a0001c0002t0009 | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1865G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1865 | chr2 | 171322307 | |||||
chr2:171322430
|
T | C | 13 | a0001c0001t0003a0001c0001t0013a0001c0001t0028others(10): Show | 41 | HG00408.hp2 HG00621.hp2 HG01167.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1742A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1742 | chr2 | 171322430 | |||||
chr2:171322431
|
G | A | 5 | a0001c0001t0013a0001c0001t0036a0001c0001t0037others(2): Show | 8 | HG02486.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1741C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1741 | chr2 | 171322431 | |||||
chr2:171322462
|
C | T | 3 | a0001c0001t0006a0001c0001t0047a0001c0001t0059 | 11 | HG00621.hp1 HG02129.hp1 HG02132.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1710G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1710 | chr2 | 171322462 | |||||
chr2:171322564
|
G | A | 1 | a0001c0001t0044 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1608C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1608 | chr2 | 171322564 | |||||
chr2:171322579
|
A | G | 1 | a0001c0002t0027 | 2 | HG01884.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1593T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1593 | chr2 | 171322579 | |||||
chr2:171322580
|
C | CA | 19 | a0001c0001t0004a0001c0001t0010a0001c0001t0011others(16): Show | 55 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1591dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1591 | chr2 | 171322580 | |||||
chr2:171322580
|
CA | C | 2 | a0001c0001t0026a0001c0002t0009 | 9 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1591delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1591 | chr2 | 171322580 | |||||
chr2:171322660
|
C | T | 1 | a0001c0002t0054 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1512G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1512 | chr2 | 171322660 | |||||
chr2:171322743
|
CAA | C | 26 | a0001c0001t0029a0001c0001t0043a0001c0001t0044others(23): Show | 42 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1427_*1428delTT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1427 | chr2 | 171322743 | |||||
chr2:171322743
|
CAAA | C | 75 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(72): Show | 282 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*1426_*1428delTTT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1426 | chr2 | 171322743 | |||||
chr2:171323116
|
C | G | 1 | a0001c0005t0015 | 4 | HG02055.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1056G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1056 | chr2 | 171323116 | |||||
chr2:171323169
|
A | C | 1 | a0001c0005t0015 | 4 | HG02055.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1003T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 1003 | chr2 | 171323169 | |||||
chr2:171323223
|
T | G | 1 | a0001c0001t0045 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*949A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 949 | chr2 | 171323223 | |||||
chr2:171323226
|
C | CT | 51 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(48): Show | 199 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*945dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 945 | chr2 | 171323226 | |||||
chr2:171323226
|
C | CTT | 24 | a0001c0001t0008a0001c0001t0023a0001c0001t0040others(21): Show | 31 | HG00280.hp1 HG00423.hp2 HG00621.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*944_*945dupAA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 945 | chr2 | 171323226 | |||||
chr2:171323226
|
CT | C | 5 | a0001c0001t0004a0001c0001t0011a0001c0001t0030others(2): Show | 30 | HG01175.hp2 HG01255.hp2 HG01934.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*945delA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 945 | chr2 | 171323226 | |||||
chr2:171323287
|
G | A | 1 | a0005c0007t0031 | 2 | HG02647.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*885C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 885 | chr2 | 171323287 | |||||
chr2:171323325
|
C | T | 1 | a0001c0001t0024 | 2 | HG02976.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*847G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 847 | chr2 | 171323325 | |||||
chr2:171323358
|
T | C | 2 | a0001c0003t0021a0001c0003t0085 | 4 | HG02258.hp1 HG02559.hp2 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*814A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 814 | chr2 | 171323358 | |||||
chr2:171323392
|
C | T | 1 | a0002c0014t0046 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*780G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 780 | chr2 | 171323392 | |||||
chr2:171323433
|
C | T | 8 | a0001c0001t0002a0001c0001t0023a0001c0001t0043others(5): Show | 36 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*739G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 739 | chr2 | 171323433 | |||||
chr2:171323470
|
C | G | 103 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(100): Show | 330 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(327): Show |
3_prime_UTR_variant | MODIFIER | c.*702G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 702 | chr2 | 171323470 | |||||
chr2:171323641
|
C | A | 1 | a0001c0003t0086 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*531G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 531 | chr2 | 171323641 | |||||
chr2:171323678
|
A | C | 1 | a0001c0001t0042 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*494T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 494 | chr2 | 171323678 | |||||
chr2:171323718
|
G | T | 2 | a0001c0001t0040a0001c0001t0041 | 2 | NA18906.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*454C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 454 | chr2 | 171323718 | |||||
chr2:171323822
|
T | C | 2 | a0001c0002t0087a0001c0003t0088 | 2 | HG03453.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*350A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 10/10 | 350 | chr2 | 171323822 | |||||
chr2:171433946
|
C | G | 5 | a0001c0001t0013a0001c0001t0036a0001c0001t0037others(2): Show | 8 | HG02486.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-76G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/10 | 41761 | chr2 | 171433946 | |||||
chr2:171433987
|
G | A | 10 | a0001c0002t0022a0001c0002t0033a0001c0002t0035others(7): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-117C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/10 | 41802 | chr2 | 171433987 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:171324424
|
G | A | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.1034-62C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171324424 | ||||||
chr2:171324680
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1034-318T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171324680 | ||||||
chr2:171324712
|
T | G | 37 | a0001c0001t0029g0252a0001c0002t0022g0317a0001c0002t0022g0318others(34): Show | 37 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1034-350A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171324712 | ||||||
chr2:171324964
|
C | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.1034-602G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171324964 | ||||||
chr2:171324981
|
TCAGCTAC others(17): Show |
T | 76 | a0001c0001t0001g0086a0001c0001t0001g0128a0001c0001t0001g0160others(73): Show | 76 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1034-643_1034-620d others(26): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171324981 | ||||||
chr2:171325047
|
G | A | 1 | a0001c0001t0003g0127 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1034-685C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171325047 | ||||||
chr2:171325049
|
G | A | 1 | a0001c0001t0003g0295 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1034-687C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171325049 | ||||||
chr2:171325051
|
G | A | 4 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1034-689C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171325051 | ||||||
chr2:171325121
|
C | CA | 49 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(46): Show | 49 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1033+719dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171325121 | ||||||
chr2:171325121
|
C | CAA | 25 | a0001c0001t0029g0252a0001c0001t0044g0162a0001c0002t0029g0056others(22): Show | 25 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1033+718_1033+719d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171325121 | ||||||
chr2:171325121
|
CA | C | 8 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(5): Show | 8 | HG01168.hp2 HG01993.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1033+719delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171325121 | ||||||
chr2:171325326
|
C | T | 97 | a0001c0001t0001g0038a0001c0001t0001g0059a0001c0001t0001g0086others(94): Show | 97 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1033+515G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171325326 | ||||||
chr2:171325344
|
C | T | 1 | a0007c0013t0082g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1033+497G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171325344 | ||||||
chr2:171325394
|
T | G | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.1033+447A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171325394 | ||||||
chr2:171325640
|
G | GT | 323 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(320): Show | 325 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(322): Show |
intron_variant | MODIFIER | c.1033+200dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171325640 | ||||||
chr2:171325782
|
G | A | 31 | a0001c0001t0029g0252a0001c0002t0054g0016a0001c0002t0072g0017others(28): Show | 31 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1033+59C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 9/9 | chr2 | 171325782 | ||||||
chr2:171325915
|
A | G | 1 | a0008c0010t0032g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.968-9T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 8/9 | chr2 | 171325915 | ||||||
chr2:171326447
|
T | C | 31 | a0001c0001t0029g0252a0001c0002t0054g0016a0001c0002t0072g0017others(28): Show | 31 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.861-299A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171326447 | ||||||
chr2:171326566
|
G | A | 1 | a0001c0003t0055g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.861-418C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171326566 | ||||||
chr2:171326587
|
C | T | 4 | a0001c0005t0015g0099a0001c0005t0015g0100a0001c0005t0015g0101others(1): Show | 4 | HG02055.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.861-439G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171326587 | ||||||
chr2:171326617
|
C | T | 1 | a0001c0001t0004g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.861-469G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171326617 | ||||||
chr2:171326618
|
G | A | 86 | a0001c0001t0024g0102a0001c0001t0024g0207a0001c0001t0074g0090others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.861-470C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171326618 | ||||||
chr2:171326702
|
TTTAA | T | 27 | a0001c0001t0074g0090a0001c0002t0007g0298a0001c0002t0007g0303others(24): Show | 27 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.861-558_861-555del others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171326702 | ||||||
chr2:171326774
|
C | A | 2 | a0001c0001t0002g0214a0001c0001t0002g0215 | 2 | NA19005.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.861-626G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171326774 | ||||||
chr2:171327427
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.861-1279A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171327427 | ||||||
chr2:171327463
|
G | C | 4 | a0003c0006t0001g0129a0003c0006t0001g0130a0003c0006t0001g0152others(1): Show | 4 | NA18947.hp1 NA18971.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-1315C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171327463 | ||||||
chr2:171327847
|
T | G | 1 | a0001c0005t0015g0099 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.861-1699A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171327847 | ||||||
chr2:171327870
|
C | T | 10 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(7): Show | 10 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.861-1722G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171327870 | ||||||
chr2:171327871
|
G | A | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.861-1723C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171327871 | ||||||
chr2:171328072
|
T | A | 1 | a0006c0015t0002g0190 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.861-1924A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171328072 | ||||||
chr2:171328227
|
G | GGAAAA | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.861-2080_861-2079i others(7): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171328227 | ||||||
chr2:171328304
|
G | A | 4 | a0001c0005t0015g0099a0001c0005t0015g0100a0001c0005t0015g0101others(1): Show | 4 | HG02055.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.861-2156C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171328304 | ||||||
chr2:171328347
|
C | T | 1 | a0001c0001t0078g0294 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.861-2199G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171328347 | ||||||
chr2:171328406
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.860+2153A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171328406 | ||||||
chr2:171328572
|
G | A | 29 | a0001c0001t0024g0102a0001c0001t0024g0207a0001c0001t0074g0090others(26): Show | 29 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.860+1987C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171328572 | ||||||
chr2:171328699
|
T | G | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.860+1860A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171328699 | ||||||
chr2:171328751
|
A | G | 1 | a0001c0001t0002g0161 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.860+1808T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171328751 | ||||||
chr2:171328849
|
C | T | 30 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0005g0021others(27): Show | 30 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.860+1710G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171328849 | ||||||
chr2:171328888
|
C | G | 2 | a0002c0004t0034g0328a0002c0004t0034g0329 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.860+1671G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171328888 | ||||||
chr2:171328993
|
A | AT | 36 | a0001c0001t0024g0102a0001c0001t0024g0207a0001c0001t0074g0090others(33): Show | 36 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.860+1565dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171328993 | ||||||
chr2:171329012
|
G | T | 12 | a0001c0002t0001g0002a0001c0002t0001g0054a0001c0002t0001g0218others(9): Show | 13 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.860+1547C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171329012 | ||||||
chr2:171329086
|
A | G | 24 | a0001c0001t0074g0090a0001c0002t0007g0298a0001c0002t0007g0303others(21): Show | 24 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.860+1473T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171329086 | ||||||
chr2:171329092
|
T | G | 1 | a0001c0001t0016g0061 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.860+1467A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171329092 | ||||||
chr2:171329105
|
C | T | 1 | a0001c0005t0015g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.860+1454G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171329105 | ||||||
chr2:171329128
|
G | A | 29 | a0001c0001t0024g0102a0001c0001t0024g0207a0001c0001t0074g0090others(26): Show | 29 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.860+1431C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171329128 | ||||||
chr2:171329144
|
C | G | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.860+1415G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171329144 | ||||||
chr2:171329242
|
C | T | 29 | a0001c0001t0024g0102a0001c0001t0024g0207a0001c0001t0074g0090others(26): Show | 29 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.860+1317G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171329242 | ||||||
chr2:171329338
|
T | A | 1 | a0001c0001t0006g0200 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.860+1221A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171329338 | ||||||
chr2:171329417
|
C | T | 1 | a0001c0002t0001g0002 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.860+1142G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171329417 | ||||||
chr2:171329811
|
C | T | 11 | a0001c0001t0001g0037a0001c0002t0009g0249a0001c0002t0009g0269others(8): Show | 11 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.860+748G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171329811 | ||||||
chr2:171330105
|
G | A | 1 | a0001c0001t0013g0008 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.860+454C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171330105 | ||||||
chr2:171330400
|
G | A | 27 | a0001c0001t0074g0090a0001c0002t0007g0298a0001c0002t0007g0303others(24): Show | 27 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.860+159C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171330400 | ||||||
chr2:171330477
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.860+82A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171330477 | ||||||
chr2:171330531
|
T | G | 1 | a0001c0001t0004g0268 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.860+28A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171330531 | ||||||
chr2:171330534
|
A | G | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.860+25T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 7/9 | chr2 | 171330534 | ||||||
chr2:171331043
|
A | G | 5 | a0001c0002t0054g0016a0001c0002t0072g0017a0005c0007t0005g0235others(2): Show | 5 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-345T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 6/9 | chr2 | 171331043 | ||||||
chr2:171331160
|
G | C | 1 | a0001c0002t0048g0312 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.721-462C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 6/9 | chr2 | 171331160 | ||||||
chr2:171331172
|
G | A | 2 | a0001c0002t0008g0217a0001c0002t0008g0223 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.721-474C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 6/9 | chr2 | 171331172 | ||||||
chr2:171331375
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.720+429G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 6/9 | chr2 | 171331375 | ||||||
chr2:171331482
|
T | A | 1 | a0001c0001t0004g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.720+322A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 6/9 | chr2 | 171331482 | ||||||
chr2:171331519
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.720+285G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 6/9 | chr2 | 171331519 | ||||||
chr2:171331542
|
A | G | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+262T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 6/9 | chr2 | 171331542 | ||||||
chr2:171331918
|
C | T | 1 | a0001c0001t0003g0119 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.657-51G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171331918 | ||||||
chr2:171331919
|
G | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.657-52C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171331919 | ||||||
chr2:171332217
|
TACTC | T | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-354_657-351del others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171332217 | ||||||
chr2:171332313
|
C | T | 1 | a0001c0001t0010g0257 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.657-446G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171332313 | ||||||
chr2:171332440
|
G | A | 1 | a0001c0002t0093g0322 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.657-573C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171332440 | ||||||
chr2:171332633
|
C | A | 4 | a0001c0001t0012g0049a0001c0001t0012g0050a0001c0001t0012g0051others(1): Show | 4 | HG02145.hp1 HG02622.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-766G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171332633 | ||||||
chr2:171332791
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.657-924A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171332791 | ||||||
chr2:171332853
|
T | C | 1 | a0001c0001t0041g0194 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.657-986A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171332853 | ||||||
chr2:171332929
|
G | A | 1 | a0001c0002t0001g0221 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.657-1062C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171332929 | ||||||
chr2:171333010
|
T | TCTAAATA others(18): Show |
33 | a0001c0001t0001g0111a0001c0001t0003g0001a0001c0001t0003g0075others(30): Show | 34 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.657-1168_657-1144d others(27): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171333010 | ||||||
chr2:171333028
|
T | A | 89 | a0001c0001t0074g0090a0001c0002t0001g0002a0001c0002t0001g0044others(86): Show | 90 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.657-1161A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171333028 | ||||||
chr2:171333029
|
T | C | 89 | a0001c0001t0074g0090a0001c0002t0001g0002a0001c0002t0001g0044others(86): Show | 90 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.657-1162A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171333029 | ||||||
chr2:171333030
|
ATTT | A | 89 | a0001c0001t0074g0090a0001c0002t0001g0002a0001c0002t0001g0044others(86): Show | 90 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.657-1166_657-1164d others(5): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171333030 | ||||||
chr2:171333036
|
CTAA | C | 89 | a0001c0001t0074g0090a0001c0002t0001g0002a0001c0002t0001g0044others(86): Show | 90 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.657-1172_657-1170d others(5): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171333036 | ||||||
chr2:171333040
|
A | C | 89 | a0001c0001t0074g0090a0001c0002t0001g0002a0001c0002t0001g0044others(86): Show | 90 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.657-1173T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171333040 | ||||||
chr2:171333041
|
T | C | 89 | a0001c0001t0074g0090a0001c0002t0001g0002a0001c0002t0001g0044others(86): Show | 90 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.657-1174A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171333041 | ||||||
chr2:171333100
|
C | CT | 143 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(140): Show | 144 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.657-1234dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171333100 | ||||||
chr2:171333239
|
C | T | 41 | a0001c0001t0001g0264a0001c0001t0001g0288a0001c0001t0004g0242others(38): Show | 41 | HG01109.hp2 HG01175.hp2 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.657-1372G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171333239 | ||||||
chr2:171333255
|
C | T | 33 | a0001c0001t0001g0111a0001c0001t0003g0001a0001c0001t0003g0075others(30): Show | 34 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.657-1388G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171333255 | ||||||
chr2:171333533
|
G | A | 1 | a0001c0001t0037g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.657-1666C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171333533 | ||||||
chr2:171333917
|
A | G | 4 | a0001c0005t0015g0099a0001c0005t0015g0100a0001c0005t0015g0101others(1): Show | 4 | HG02055.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-2050T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171333917 | ||||||
chr2:171334071
|
T | TAAAAC | 15 | a0001c0001t0001g0037a0001c0001t0001g0315a0001c0001t0059g0188others(12): Show | 15 | HG00408.hp1 HG00597.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.657-2209_657-2205d others(7): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171334071 | ||||||
chr2:171334071
|
T | TAAAACAA others(3): Show |
2 | a0001c0001t0040g0198a0001c0001t0041g0194 | 2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.657-2214_657-2205d others(12): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171334071 | ||||||
chr2:171334071
|
T | TAAAACAA others(8): Show |
2 | a0001c0001t0001g0197a0001c0001t0008g0169 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.657-2219_657-2205d others(17): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171334071 | ||||||
chr2:171334071
|
TAAAAC | T | 52 | a0001c0001t0001g0055a0001c0001t0001g0145a0001c0002t0001g0002others(49): Show | 53 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.657-2209_657-2205d others(7): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171334071 | ||||||
chr2:171334071
|
TAAAACAA others(3): Show |
T | 1 | a0001c0001t0003g0082 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.657-2214_657-2205d others(12): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171334071 | ||||||
chr2:171334138
|
T | C | 1 | a0001c0002t0001g0226 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.657-2271A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171334138 | ||||||
chr2:171334223
|
T | C | 1 | a0005c0007t0031g0018 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.657-2356A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171334223 | ||||||
chr2:171334230
|
C | T | 1 | a0001c0001t0004g0279 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.657-2363G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171334230 | ||||||
chr2:171334262
|
A | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.657-2395T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171334262 | ||||||
chr2:171334331
|
G | C | 7 | a0002c0004t0018g0072a0002c0004t0018g0073a0002c0004t0018g0092others(4): Show | 7 | HG01074.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.657-2464C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171334331 | ||||||
chr2:171334418
|
G | A | 4 | a0001c0005t0015g0099a0001c0005t0015g0100a0001c0005t0015g0101others(1): Show | 4 | HG02055.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-2551C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171334418 | ||||||
chr2:171334672
|
G | A | 4 | a0001c0001t0001g0288a0001c0001t0010g0285a0001c0001t0010g0286others(1): Show | 4 | HG01258.hp1 HG01433.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+2781C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171334672 | ||||||
chr2:171334720
|
A | G | 1 | a0002c0014t0046g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.656+2733T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171334720 | ||||||
chr2:171334935
|
A | G | 1 | a0001c0001t0045g0241 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.656+2518T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171334935 | ||||||
chr2:171335039
|
C | T | 1 | a0001c0001t0011g0258 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.656+2414G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171335039 | ||||||
chr2:171335138
|
A | G | 1 | a0001c0001t0003g0125 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.656+2315T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171335138 | ||||||
chr2:171335184
|
T | C | 1 | a0001c0001t0002g0186 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.656+2269A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171335184 | ||||||
chr2:171335279
|
G | C | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.656+2174C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171335279 | ||||||
chr2:171335432
|
A | T | 1 | a0001c0002t0057g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.656+2021T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171335432 | ||||||
chr2:171335470
|
G | A | 1 | a0001c0002t0091g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.656+1983C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171335470 | ||||||
chr2:171335507
|
C | A | 4 | a0001c0001t0017g0053a0001c0001t0017g0204a0001c0001t0017g0212others(1): Show | 4 | HG02602.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+1946G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171335507 | ||||||
chr2:171335550
|
G | A | 1 | a0001c0001t0028g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.656+1903C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171335550 | ||||||
chr2:171335677
|
G | A | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.656+1776C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171335677 | ||||||
chr2:171335730
|
T | C | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.656+1723A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171335730 | ||||||
chr2:171335735
|
T | C | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.656+1718A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171335735 | ||||||
chr2:171336142
|
G | A | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.656+1311C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336142 | ||||||
chr2:171336191
|
G | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.656+1262C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336191 | ||||||
chr2:171336215
|
C | A | 1 | a0001c0001t0014g0216 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.656+1238G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336215 | ||||||
chr2:171336220
|
C | A | 3 | a0001c0002t0035g0326a0001c0002t0035g0327a0001c0002t0093g0322 | 3 | HG03540.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.656+1233G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336220 | ||||||
chr2:171336241
|
G | A | 1 | a0001c0002t0061g0314 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.656+1212C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336241 | ||||||
chr2:171336301
|
T | C | 1 | a0001c0001t0006g0199 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.656+1152A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336301 | ||||||
chr2:171336309
|
C | A | 1 | a0001c0001t0001g0098 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.656+1144G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336309 | ||||||
chr2:171336396
|
CT | C | 22 | a0001c0001t0001g0040a0001c0001t0001g0151a0001c0001t0002g0087others(19): Show | 22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.656+1056delA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336396 | ||||||
chr2:171336396
|
CTT | C | 218 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(215): Show | 219 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.656+1055_656+1056d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336396 | ||||||
chr2:171336396
|
CTTT | C | 76 | a0001c0001t0001g0138a0001c0001t0001g0157a0001c0001t0001g0205others(73): Show | 77 | HG00280.hp1 HG00423.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.656+1054_656+1056d others(5): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336396 | ||||||
chr2:171336441
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.656+1012C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336441 | ||||||
chr2:171336550
|
C | T | 3 | a0001c0001t0017g0204a0001c0001t0017g0212a0001c0001t0051g0211 | 3 | HG02602.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.656+903G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336550 | ||||||
chr2:171336863
|
C | CT | 46 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0155others(43): Show | 46 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.656+589dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336863 | ||||||
chr2:171336863
|
C | CTT | 24 | a0001c0001t0074g0090a0001c0002t0007g0298a0001c0002t0007g0306others(21): Show | 24 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.656+588_656+589dup others(2): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336863 | ||||||
chr2:171336863
|
C | CTTT | 10 | a0001c0002t0001g0002a0001c0002t0001g0054a0001c0002t0001g0218others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.656+587_656+589dup others(3): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336863 | ||||||
chr2:171336863
|
CT | C | 7 | a0001c0001t0001g0037a0001c0001t0001g0138a0001c0001t0002g0048others(4): Show | 7 | HG00280.hp2 HG01256.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.656+589delA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336863 | ||||||
chr2:171336863
|
CTT | C | 17 | a0001c0001t0003g0001a0001c0001t0003g0075a0001c0001t0003g0076others(14): Show | 18 | HG00408.hp2 HG00621.hp2 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.656+588_656+589del others(2): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336863 | ||||||
chr2:171336863
|
CTTTTT | C | 6 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(3): Show | 6 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.656+585_656+589del others(5): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171336863 | ||||||
chr2:171337251
|
C | T | 3 | a0001c0002t0035g0326a0001c0002t0035g0327a0001c0002t0093g0322 | 3 | HG03540.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.656+202G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171337251 | ||||||
chr2:171337298
|
T | C | 94 | a0001c0001t0024g0102a0001c0001t0024g0207a0001c0001t0029g0252others(91): Show | 95 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.656+155A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171337298 | ||||||
chr2:171337434
|
G | T | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.656+19C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 5/9 | chr2 | 171337434 | ||||||
chr2:171337618
|
G | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.607-116C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171337618 | ||||||
chr2:171337667
|
C | T | 1 | a0001c0001t0004g0273 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.607-165G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171337667 | ||||||
chr2:171337796
|
G | GA | 9 | a0001c0001t0002g0177a0001c0001t0002g0189a0001c0002t0009g0249others(6): Show | 9 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.607-295dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171337796 | ||||||
chr2:171337844
|
A | G | 1 | a0001c0002t0009g0292 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.607-342T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171337844 | ||||||
chr2:171337916
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.607-414G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171337916 | ||||||
chr2:171338297
|
T | C | 1 | a0002c0009t0066g0091 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.607-795A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171338297 | ||||||
chr2:171338408
|
C | A | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.606+776G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171338408 | ||||||
chr2:171338478
|
A | G | 12 | a0001c0002t0001g0002a0001c0002t0001g0054a0001c0002t0001g0218others(9): Show | 13 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.606+706T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171338478 | ||||||
chr2:171338481
|
T | C | 1 | a0001c0002t0061g0314 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.606+703A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171338481 | ||||||
chr2:171338483
|
CA | C | 4 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+700delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171338483 | ||||||
chr2:171338565
|
G | A | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.606+619C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171338565 | ||||||
chr2:171338614
|
C | T | 1 | a0001c0002t0029g0056 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.606+570G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171338614 | ||||||
chr2:171338640
|
CA | C | 6 | a0001c0001t0001g0283a0001c0001t0002g0048a0001c0001t0004g0273others(3): Show | 6 | NA18941.hp1 NA18951.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+543delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171338640 | ||||||
chr2:171338828
|
A | G | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.606+356T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171338828 | ||||||
chr2:171338911
|
T | C | 116 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(113): Show | 116 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.606+273A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171338911 | ||||||
chr2:171338967
|
A | T | 6 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0290others(3): Show | 6 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.606+217T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171338967 | ||||||
chr2:171339024
|
T | C | 3 | a0001c0001t0003g0121a0001c0001t0003g0127a0001c0001t0028g0113 | 3 | HG03669.hp1 HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.606+160A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171339024 | ||||||
chr2:171339035
|
G | A | 324 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(321): Show | 326 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(323): Show |
intron_variant | MODIFIER | c.606+149C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171339035 | ||||||
chr2:171339142
|
A | C | 1 | a0001c0001t0003g0093 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.606+42T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 4/9 | chr2 | 171339142 | ||||||
chr2:171339592
|
C | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-38G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171339592 | ||||||
chr2:171339635
|
C | G | 2 | a0001c0001t0011g0259a0001c0001t0079g0261 | 2 | NA18982.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.236-81G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171339635 | ||||||
chr2:171339921
|
A | G | 82 | a0001c0001t0029g0252a0001c0001t0074g0090a0001c0002t0001g0002others(79): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.236-367T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171339921 | ||||||
chr2:171339925
|
G | A | 2 | a0005c0007t0031g0018a0005c0007t0031g0020 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.236-371C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171339925 | ||||||
chr2:171339927
|
G | A | 1 | a0001c0001t0026g0150 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.236-373C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171339927 | ||||||
chr2:171340198
|
CA | C | 314 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(311): Show | 316 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.236-645delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171340198 | ||||||
chr2:171340386
|
C | T | 36 | a0001c0001t0001g0170a0001c0001t0002g0011a0001c0001t0002g0012others(33): Show | 36 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.236-832G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171340386 | ||||||
chr2:171340498
|
C | CA | 35 | a0001c0001t0001g0206a0001c0001t0002g0048a0001c0001t0002g0161others(32): Show | 36 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.236-945dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171340498 | ||||||
chr2:171340498
|
C | CAA | 7 | a0001c0001t0016g0062a0001c0002t0001g0227a0001c0002t0009g0249others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-946_236-945dup others(2): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171340498 | ||||||
chr2:171340498
|
CA | C | 11 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0095others(8): Show | 11 | HG01069.hp1 HG01081.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.236-945delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171340498 | ||||||
chr2:171340498
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0005t0015g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.236-956_236-945del others(12): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171340498 | ||||||
chr2:171340567
|
A | ATAAG | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-1014_236-1013i others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171340567 | ||||||
chr2:171340568
|
T | C | 120 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0057others(117): Show | 121 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(118): Show |
intron_variant | MODIFIER | c.236-1014A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171340568 | ||||||
chr2:171340572
|
TAAAC | T | 5 | a0001c0002t0054g0016a0001c0002t0072g0017a0005c0007t0005g0235others(2): Show | 5 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-1022_236-1019d others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171340572 | ||||||
chr2:171340678
|
C | G | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-1124G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171340678 | ||||||
chr2:171341095
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.236-1541G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341095 | ||||||
chr2:171341188
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-1634A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341188 | ||||||
chr2:171341201
|
G | A | 1 | a0001c0001t0050g0208 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.236-1647C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341201 | ||||||
chr2:171341285
|
G | A | 24 | a0001c0001t0074g0090a0001c0002t0007g0298a0001c0002t0007g0303others(21): Show | 24 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.236-1731C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341285 | ||||||
chr2:171341292
|
C | T | 1 | a0001c0001t0010g0257 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.236-1738G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341292 | ||||||
chr2:171341327
|
C | CA | 37 | a0001c0001t0002g0177a0001c0001t0011g0266a0001c0001t0078g0294others(34): Show | 37 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.236-1774dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341327 | ||||||
chr2:171341504
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.236-1950C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341504 | ||||||
chr2:171341555
|
C | CT | 10 | a0001c0001t0011g0266a0001c0002t0035g0326a0001c0002t0035g0327others(7): Show | 10 | HG01074.hp1 HG02280.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.236-2002dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341555 | ||||||
chr2:171341555
|
CT | C | 10 | a0001c0001t0001g0043a0001c0001t0047g0166a0001c0001t0059g0188others(7): Show | 10 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.236-2002delA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341555 | ||||||
chr2:171341573
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-2019A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341573 | ||||||
chr2:171341791
|
TAAG | T | 20 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(17): Show | 20 | HG01069.hp1 HG01433.hp1 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.236-2240_236-2238d others(5): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341791 | ||||||
chr2:171341804
|
C | T | 4 | a0001c0001t0016g0061a0001c0001t0016g0062a0001c0001t0016g0064others(1): Show | 4 | NA18952.hp2 NA18953.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-2250G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341804 | ||||||
chr2:171341834
|
T | TAC | 48 | a0001c0001t0001g0039a0001c0001t0001g0042a0001c0001t0001g0057others(45): Show | 48 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.236-2282_236-2281d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341834 | ||||||
chr2:171341834
|
T | TACAC | 17 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0043others(14): Show | 17 | HG02055.hp2 HG02056.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.236-2284_236-2281d others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341834 | ||||||
chr2:171341834
|
T | TACACAC | 4 | a0001c0002t0033g0324a0001c0002t0090g0323a0001c0002t0092g0321others(1): Show | 4 | HG01261.hp1 HG02280.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-2286_236-2281d others(8): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341834 | ||||||
chr2:171341834
|
TAC | T | 74 | a0001c0001t0001g0037a0001c0001t0001g0144a0001c0001t0001g0145others(71): Show | 74 | HG00280.hp1 HG00423.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.236-2282_236-2281d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341834 | ||||||
chr2:171341834
|
TACAC | T | 6 | a0001c0001t0001g0085a0001c0001t0001g0094a0001c0001t0014g0209others(3): Show | 6 | HG01099.hp2 HG02572.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.236-2284_236-2281d others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341834 | ||||||
chr2:171341834
|
TACACAC | T | 9 | a0001c0001t0004g0276a0001c0001t0004g0278a0001c0001t0004g0279others(6): Show | 9 | HG02818.hp2 HG03139.hp1 HG06807.hp2 others(6): Show |
intron_variant | MODIFIER | c.236-2286_236-2281d others(8): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171341834 | ||||||
chr2:171342077
|
A | C | 1 | a0001c0001t0078g0294 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.236-2523T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171342077 | ||||||
chr2:171342235
|
C | A | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-2681G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171342235 | ||||||
chr2:171342268
|
A | G | 1 | a0001c0001t0036g0003 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.236-2714T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171342268 | ||||||
chr2:171342421
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-2867A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171342421 | ||||||
chr2:171342466
|
T | G | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.236-2912A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171342466 | ||||||
chr2:171342567
|
G | A | 24 | a0001c0001t0074g0090a0001c0002t0007g0298a0001c0002t0007g0303others(21): Show | 24 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.236-3013C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171342567 | ||||||
chr2:171342595
|
T | C | 3 | a0001c0003t0019g0019a0001c0003t0055g0015a0001c0003t0088g0014 | 3 | HG02717.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.236-3041A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171342595 | ||||||
chr2:171342615
|
T | TA | 10 | a0001c0001t0001g0037a0001c0002t0035g0326a0001c0002t0035g0327others(7): Show | 10 | HG01074.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.236-3062dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171342615 | ||||||
chr2:171342615
|
TA | T | 112 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(109): Show | 112 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.236-3062delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171342615 | ||||||
chr2:171342660
|
G | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-3106C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171342660 | ||||||
chr2:171342894
|
G | A | 5 | a0001c0002t0001g0218a0001c0002t0001g0221a0001c0002t0001g0222others(2): Show | 5 | HG02451.hp2 HG02486.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-3340C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171342894 | ||||||
chr2:171343161
|
G | A | 7 | a0001c0001t0074g0090a0001c0002t0033g0324a0001c0002t0033g0330others(4): Show | 7 | HG01261.hp1 HG02895.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-3607C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343161 | ||||||
chr2:171343189
|
C | T | 1 | a0005c0007t0031g0018 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.236-3635G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343189 | ||||||
chr2:171343237
|
C | T | 2 | a0002c0004t0034g0328a0002c0004t0034g0329 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.236-3683G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343237 | ||||||
chr2:171343240
|
G | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-3686C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343240 | ||||||
chr2:171343248
|
T | A | 53 | a0001c0001t0001g0264a0001c0001t0001g0288a0001c0001t0003g0295others(50): Show | 53 | HG01109.hp2 HG01175.hp2 HG01255.hp2 others(50): Show |
intron_variant | MODIFIER | c.236-3694A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343248 | ||||||
chr2:171343266
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.236-3712G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343266 | ||||||
chr2:171343299
|
T | C | 319 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(316): Show | 321 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.236-3745A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343299 | ||||||
chr2:171343338
|
C | T | 1 | a0001c0002t0001g0221 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.236-3784G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343338 | ||||||
chr2:171343380
|
G | A | 3 | a0001c0002t0035g0326a0001c0002t0035g0327a0001c0002t0093g0322 | 3 | HG03540.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.236-3826C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343380 | ||||||
chr2:171343388
|
G | A | 3 | a0001c0002t0035g0326a0001c0002t0035g0327a0001c0002t0093g0322 | 3 | HG03540.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.236-3834C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343388 | ||||||
chr2:171343439
|
C | CAATAAAT others(9): Show |
3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.236-3901_236-3886d others(18): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343439 | ||||||
chr2:171343462
|
T | TAAATAAA others(21): Show |
3 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270 | 3 | HG00597.hp1 NA18975.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.236-3909_236-3908i others(30): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343462 | ||||||
chr2:171343462
|
T | TAAATAAA others(25): Show |
4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-3909_236-3908i others(34): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343462 | ||||||
chr2:171343535
|
C | T | 2 | a0001c0001t0002g0036a0001c0001t0002g0189 | 2 | NA18994.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.236-3981G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343535 | ||||||
chr2:171343589
|
T | G | 19 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(16): Show | 19 | HG01069.hp1 HG01109.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.236-4035A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343589 | ||||||
chr2:171343927
|
C | T | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.236-4373G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171343927 | ||||||
chr2:171344088
|
A | C | 1 | a0001c0001t0001g0213 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.236-4534T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171344088 | ||||||
chr2:171344358
|
C | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-4804G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171344358 | ||||||
chr2:171344389
|
G | A | 1 | a0001c0001t0073g0063 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.236-4835C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171344389 | ||||||
chr2:171344643
|
T | C | 2 | a0004c0008t0001g0299a0004c0008t0001g0300 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.236-5089A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171344643 | ||||||
chr2:171344774
|
G | T | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.236-5220C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171344774 | ||||||
chr2:171344989
|
C | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-5435G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171344989 | ||||||
chr2:171345336
|
T | C | 1 | a0001c0001t0059g0188 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.236-5782A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171345336 | ||||||
chr2:171345373
|
T | C | 92 | a0001c0001t0029g0252a0001c0001t0074g0090a0001c0002t0001g0002others(89): Show | 93 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.236-5819A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171345373 | ||||||
chr2:171345467
|
T | C | 1 | a0001c0001t0001g0264 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.236-5913A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171345467 | ||||||
chr2:171345488
|
TAA | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-5936_236-5935d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171345488 | ||||||
chr2:171345529
|
A | T | 2 | a0001c0001t0024g0102a0001c0001t0024g0207 | 2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.236-5975T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171345529 | ||||||
chr2:171345609
|
A | C | 4 | a0001c0001t0002g0180a0001c0001t0002g0296a0001c0001t0017g0212others(1): Show | 4 | HG00438.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-6055T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171345609 | ||||||
chr2:171345630
|
C | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-6076G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171345630 | ||||||
chr2:171345634
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-6080A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171345634 | ||||||
chr2:171345844
|
T | C | 34 | a0001c0001t0074g0090a0001c0002t0007g0298a0001c0002t0007g0303others(31): Show | 34 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.236-6290A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171345844 | ||||||
chr2:171345864
|
A | C | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.236-6310T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171345864 | ||||||
chr2:171345934
|
T | C | 1 | a0001c0002t0072g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.236-6380A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171345934 | ||||||
chr2:171346009
|
C | G | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.236-6455G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171346009 | ||||||
chr2:171346023
|
TTTTTTG | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-6475_236-6470d others(8): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171346023 | ||||||
chr2:171346313
|
C | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-6759G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171346313 | ||||||
chr2:171346456
|
A | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG00438.hp2 HG02080.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.236-6902T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171346456 | ||||||
chr2:171346738
|
G | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-7184C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171346738 | ||||||
chr2:171346823
|
G | A | 1 | a0007c0013t0082g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.236-7269C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171346823 | ||||||
chr2:171346982
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-7428A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171346982 | ||||||
chr2:171347045
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-7491A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171347045 | ||||||
chr2:171347227
|
C | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-7673G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171347227 | ||||||
chr2:171347326
|
C | T | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-7772G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171347326 | ||||||
chr2:171347491
|
G | A | 1 | a0009c0011t0004g0196 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.236-7937C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171347491 | ||||||
chr2:171347513
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-7959A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171347513 | ||||||
chr2:171347528
|
T | C | 2 | a0001c0001t0002g0036a0001c0001t0002g0189 | 2 | NA18994.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.236-7974A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171347528 | ||||||
chr2:171347739
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-8185A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171347739 | ||||||
chr2:171347805
|
C | T | 2 | a0001c0002t0007g0308a0001c0002t0007g0309 | 2 | HG01081.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.236-8251G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171347805 | ||||||
chr2:171347847
|
C | T | 236 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(233): Show | 237 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.236-8293G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171347847 | ||||||
chr2:171347850
|
T | C | 1 | a0003c0006t0001g0153 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.236-8296A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171347850 | ||||||
chr2:171347869
|
G | A | 4 | a0001c0001t0012g0049a0001c0001t0012g0050a0001c0001t0012g0051others(1): Show | 4 | HG02145.hp1 HG02622.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-8315C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171347869 | ||||||
chr2:171348102
|
C | G | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-8548G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171348102 | ||||||
chr2:171348371
|
G | A | 86 | a0001c0001t0029g0252a0001c0001t0074g0090a0001c0002t0001g0002others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.236-8817C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171348371 | ||||||
chr2:171348435
|
A | G | 1 | a0001c0001t0004g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.236-8881T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171348435 | ||||||
chr2:171348453
|
C | T | 2 | a0005c0007t0031g0018a0005c0007t0031g0020 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.236-8899G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171348453 | ||||||
chr2:171348493
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.236-8939C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171348493 | ||||||
chr2:171348574
|
A | C | 7 | a0002c0004t0018g0072a0002c0004t0018g0073a0002c0004t0018g0092others(4): Show | 7 | HG01074.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-9020T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171348574 | ||||||
chr2:171348626
|
C | G | 1 | a0002c0004t0018g0073 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.236-9072G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171348626 | ||||||
chr2:171348947
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-9393A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171348947 | ||||||
chr2:171349077
|
T | C | 2 | a0001c0001t0004g0262a0001c0001t0004g0263 | 2 | NA18992.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.236-9523A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171349077 | ||||||
chr2:171349625
|
T | C | 1 | a0001c0002t0001g0002 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.236-10071A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171349625 | ||||||
chr2:171349833
|
T | C | 32 | a0001c0001t0001g0111a0001c0001t0003g0001a0001c0001t0003g0075others(29): Show | 33 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.236-10279A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171349833 | ||||||
chr2:171349867
|
T | C | 1 | a0001c0001t0050g0208 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.236-10313A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171349867 | ||||||
chr2:171349914
|
C | T | 1 | a0001c0003t0005g0107 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.236-10360G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171349914 | ||||||
chr2:171349948
|
C | G | 1 | a0001c0001t0001g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.236-10394G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171349948 | ||||||
chr2:171349958
|
G | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-10404C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171349958 | ||||||
chr2:171349970
|
A | G | 2 | a0001c0001t0003g0109a0001c0001t0003g0114 | 2 | NA18973.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.236-10416T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171349970 | ||||||
chr2:171349976
|
G | A | 85 | a0001c0001t0074g0090a0001c0002t0001g0002a0001c0002t0001g0044others(82): Show | 86 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.236-10422C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171349976 | ||||||
chr2:171349994
|
A | G | 319 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(316): Show | 321 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.235+10428T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171349994 | ||||||
chr2:171350061
|
C | T | 1 | a0001c0001t0045g0241 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.235+10361G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350061 | ||||||
chr2:171350069
|
C | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+10353G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350069 | ||||||
chr2:171350176
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+10246A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350176 | ||||||
chr2:171350204
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+10218A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350204 | ||||||
chr2:171350230
|
G | A | 38 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0132others(35): Show | 38 | HG00609.hp2 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.235+10192C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350230 | ||||||
chr2:171350362
|
C | T | 90 | a0001c0001t0074g0090a0001c0002t0001g0002a0001c0002t0001g0044others(87): Show | 91 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.235+10060G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350362 | ||||||
chr2:171350399
|
T | G | 1 | a0001c0001t0006g0193 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.235+10023A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350399 | ||||||
chr2:171350424
|
C | T | 1 | a0001c0002t0048g0312 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.235+9998G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350424 | ||||||
chr2:171350477
|
C | CA | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+9944dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350477 | ||||||
chr2:171350504
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.235+9918A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350504 | ||||||
chr2:171350578
|
G | A | 26 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0013g0009others(23): Show | 27 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.235+9844C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350578 | ||||||
chr2:171350584
|
T | G | 26 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0013g0009others(23): Show | 27 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.235+9838A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350584 | ||||||
chr2:171350607
|
C | G | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.235+9815G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350607 | ||||||
chr2:171350772
|
T | A | 8 | a0001c0001t0011g0202a0001c0001t0011g0255a0001c0001t0011g0258others(5): Show | 8 | HG01934.hp2 HG01952.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+9650A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350772 | ||||||
chr2:171350960
|
T | C | 114 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0057others(111): Show | 115 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.235+9462A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350960 | ||||||
chr2:171350988
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.235+9434A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171350988 | ||||||
chr2:171351077
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.235+9345A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171351077 | ||||||
chr2:171351441
|
T | C | 2 | a0001c0001t0004g0262a0001c0001t0004g0263 | 2 | NA18992.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.235+8981A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171351441 | ||||||
chr2:171351551
|
G | A | 18 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(15): Show | 18 | HG01069.hp1 HG01433.hp1 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.235+8871C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171351551 | ||||||
chr2:171351651
|
G | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+8771C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171351651 | ||||||
chr2:171351767
|
C | G | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+8655G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171351767 | ||||||
chr2:171351806
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.235+8616A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171351806 | ||||||
chr2:171351838
|
G | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+8584C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171351838 | ||||||
chr2:171352071
|
G | A | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+8351C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171352071 | ||||||
chr2:171352121
|
G | T | 1 | a0001c0001t0002g0201 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.235+8301C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171352121 | ||||||
chr2:171352345
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.235+8077G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171352345 | ||||||
chr2:171352473
|
C | A | 1 | a0001c0001t0002g0048 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.235+7949G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171352473 | ||||||
chr2:171352766
|
A | G | 33 | a0001c0001t0074g0090a0001c0002t0007g0298a0001c0002t0007g0303others(30): Show | 33 | HG00423.hp2 HG01074.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.235+7656T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171352766 | ||||||
chr2:171352838
|
ATC | A | 4 | a0001c0003t0021g0237a0001c0003t0021g0239a0001c0003t0021g0240others(1): Show | 4 | HG02258.hp1 HG02559.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+7582_235+7583d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171352838 | ||||||
chr2:171352884
|
G | T | 1 | a0001c0001t0043g0171 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.235+7538C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171352884 | ||||||
chr2:171352923
|
C | T | 1 | a0001c0001t0003g0081 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.235+7499G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171352923 | ||||||
chr2:171353052
|
T | C | 85 | a0001c0001t0029g0252a0001c0001t0074g0090a0001c0002t0001g0002others(82): Show | 86 | HG00280.hp1 HG00423.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.235+7370A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171353052 | ||||||
chr2:171353181
|
T | C | 1 | a0001c0002t0001g0002 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.235+7241A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171353181 | ||||||
chr2:171353238
|
C | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+7184G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171353238 | ||||||
chr2:171353263
|
G | A | 2 | a0001c0001t0002g0174a0002c0004t0018g0073 | 2 | HG02280.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.235+7159C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171353263 | ||||||
chr2:171353434
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+6988A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171353434 | ||||||
chr2:171353486
|
A | G | 1 | a0001c0002t0009g0290 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.235+6936T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171353486 | ||||||
chr2:171353521
|
G | A | 4 | a0001c0001t0001g0042a0004c0008t0001g0299a0004c0008t0001g0300others(1): Show | 4 | HG02109.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+6901C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171353521 | ||||||
chr2:171353710
|
C | T | 1 | a0001c0001t0003g0110 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.235+6712G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171353710 | ||||||
chr2:171353957
|
A | G | 1 | a0001c0001t0014g0209 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.235+6465T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171353957 | ||||||
chr2:171353988
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+6434A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171353988 | ||||||
chr2:171354026
|
C | T | 1 | a0001c0001t0078g0294 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.235+6396G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171354026 | ||||||
chr2:171354098
|
G | A | 1 | a0001c0001t0006g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.235+6324C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171354098 | ||||||
chr2:171354318
|
C | T | 1 | a0001c0001t0029g0252 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.235+6104G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171354318 | ||||||
chr2:171354369
|
T | C | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.235+6053A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171354369 | ||||||
chr2:171354399
|
T | C | 3 | a0001c0001t0006g0163a0001c0001t0006g0165a0001c0001t0006g0199 | 3 | NA18969.hp1 NA18979.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.235+6023A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171354399 | ||||||
chr2:171354605
|
G | C | 2 | a0001c0001t0047g0166a0001c0001t0059g0188 | 2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.235+5817C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171354605 | ||||||
chr2:171354680
|
A | C | 1 | a0001c0001t0084g0247 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.235+5742T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171354680 | ||||||
chr2:171354691
|
C | T | 32 | a0001c0001t0001g0111a0001c0001t0003g0001a0001c0001t0003g0075others(29): Show | 33 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.235+5731G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171354691 | ||||||
chr2:171354802
|
A | C | 30 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0005g0021others(27): Show | 30 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.235+5620T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171354802 | ||||||
chr2:171354834
|
G | A | 25 | a0001c0003t0005g0021a0001c0003t0005g0022a0001c0003t0005g0023others(22): Show | 25 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.235+5588C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171354834 | ||||||
chr2:171354863
|
A | AT | 114 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0057others(111): Show | 115 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.235+5558dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171354863 | ||||||
chr2:171354863
|
AT | A | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+5558delA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171354863 | ||||||
chr2:171354927
|
A | G | 1 | a0001c0001t0002g0177 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.235+5495T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171354927 | ||||||
chr2:171354945
|
G | A | 1 | a0001c0001t0003g0115 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.235+5477C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171354945 | ||||||
chr2:171355040
|
G | T | 2 | a0001c0001t0053g0244a0001c0001t0069g0248 | 2 | HG01109.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.235+5382C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171355040 | ||||||
chr2:171355118
|
C | T | 328 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(325): Show | 330 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.235+5304G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171355118 | ||||||
chr2:171355200
|
A | G | 7 | a0002c0004t0018g0072a0002c0004t0018g0073a0002c0004t0018g0092others(4): Show | 7 | HG01074.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+5222T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171355200 | ||||||
chr2:171355237
|
C | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+5185G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171355237 | ||||||
chr2:171355238
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.235+5184C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171355238 | ||||||
chr2:171355242
|
C | A | 2 | a0001c0003t0055g0015a0001c0003t0088g0014 | 2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.235+5180G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171355242 | ||||||
chr2:171355296
|
C | T | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+5126G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171355296 | ||||||
chr2:171355387
|
G | GTCC | 27 | a0001c0001t0074g0090a0001c0002t0007g0298a0001c0002t0007g0303others(24): Show | 27 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.235+5034_235+5035i others(5): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171355387 | ||||||
chr2:171355422
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+5000A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171355422 | ||||||
chr2:171355595
|
T | C | 5 | a0001c0001t0002g0048a0001c0001t0002g0161a0001c0001t0002g0185others(2): Show | 5 | NA18951.hp1 NA18985.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+4827A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171355595 | ||||||
chr2:171355632
|
G | A | 1 | a0002c0014t0046g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.235+4790C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171355632 | ||||||
chr2:171355636
|
G | A | 4 | a0001c0001t0004g0242a0001c0001t0004g0282a0001c0001t0004g0289others(1): Show | 4 | HG02602.hp1 NA18948.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+4786C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171355636 | ||||||
chr2:171355793
|
C | T | 37 | a0001c0001t0074g0090a0001c0002t0007g0298a0001c0002t0007g0303others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.235+4629G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171355793 | ||||||
chr2:171355860
|
G | A | 1 | a0001c0001t0003g0232 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.235+4562C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171355860 | ||||||
chr2:171356142
|
C | T | 113 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(110): Show | 113 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.235+4280G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356142 | ||||||
chr2:171356499
|
T | C | 4 | a0001c0001t0012g0049a0001c0001t0012g0050a0001c0001t0012g0051others(1): Show | 4 | HG02145.hp1 HG02622.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+3923A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356499 | ||||||
chr2:171356503
|
G | A | 112 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(109): Show | 112 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.235+3919C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356503 | ||||||
chr2:171356518
|
A | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+3904T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356518 | ||||||
chr2:171356522
|
T | TTCTA | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+3896_235+3899d others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356522 | ||||||
chr2:171356581
|
C | A | 30 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0005g0021others(27): Show | 30 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.235+3841G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356581 | ||||||
chr2:171356753
|
A | G | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+3669T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356753 | ||||||
chr2:171356827
|
C | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+3595G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356827 | ||||||
chr2:171356891
|
A | G | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.235+3531T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356891 | ||||||
chr2:171356950
|
A | ATTTTTTT others(7): Show |
3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0043 | 3 | HG02622.hp2 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.235+3471_235+3472i others(16): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356950 | ||||||
chr2:171356950
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0042 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.235+3471_235+3472i others(17): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356950 | ||||||
chr2:171356952
|
A | ATGTTTTG others(6): Show |
3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.235+3469_235+3470i others(15): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | ATGTTTTT others(1): Show |
29 | a0001c0001t0074g0090a0001c0002t0007g0298a0001c0002t0007g0303others(26): Show | 29 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.235+3469_235+3470i others(10): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | ATGTTTTT others(8): Show |
2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.235+3469_235+3470i others(17): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | ATGTTTTT others(4): Show |
8 | a0001c0001t0078g0294a0001c0002t0009g0249a0001c0002t0009g0269others(5): Show | 8 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.235+3469_235+3470i others(13): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | ATGTTTTT others(10): Show |
1 | a0001c0002t0001g0044 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.235+3469_235+3470i others(19): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | ATGTTTTT others(10): Show |
2 | a0001c0003t0005g0025a0001c0003t0005g0029 | 2 | HG01496.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.235+3469_235+3470i others(19): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | ATGTTTTT others(6): Show |
36 | a0001c0001t0001g0111a0001c0001t0001g0288a0001c0001t0003g0001others(33): Show | 37 | HG00280.hp2 HG00621.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.235+3469_235+3470i others(15): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | ATGTTTTT others(7): Show |
36 | a0001c0001t0001g0264a0001c0001t0003g0075a0001c0001t0003g0079others(33): Show | 36 | HG00408.hp2 HG01109.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.235+3469_235+3470i others(16): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | ATGTTTTT others(8): Show |
31 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0058others(28): Show | 31 | HG01069.hp1 HG01074.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.235+3469_235+3470i others(17): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | ATGTTTTT others(9): Show |
57 | a0001c0001t0001g0039a0001c0001t0001g0067a0001c0001t0001g0068others(54): Show | 57 | HG00558.hp1 HG00558.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.235+3469_235+3470i others(18): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | ATGTTTTT others(10): Show |
73 | a0001c0001t0001g0057a0001c0001t0001g0086a0001c0001t0001g0094others(70): Show | 74 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.235+3469_235+3470i others(19): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | ATGTTTTT others(11): Show |
23 | a0001c0001t0001g0128a0001c0001t0001g0146a0001c0001t0001g0154others(20): Show | 23 | HG01099.hp1 HG01106.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.235+3469_235+3470i others(20): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | ATGTTTTT others(12): Show |
10 | a0001c0001t0001g0038a0001c0001t0006g0181a0001c0001t0014g0209others(7): Show | 10 | HG02055.hp1 HG02129.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.235+3469_235+3470i others(21): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | ATGTTTTT others(13): Show |
1 | a0001c0002t0001g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.235+3469_235+3470i others(22): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | ATGTTTTT others(14): Show |
1 | a0001c0001t0008g0046 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.235+3469_235+3470i others(23): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | ATGTTTTT others(16): Show |
1 | a0007c0013t0082g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.235+3469_235+3470i others(25): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356952
|
A | T | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+3470T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356952 | ||||||
chr2:171356956
|
T | G | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+3466A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356956 | ||||||
chr2:171356960
|
T | C | 3 | a0001c0003t0019g0019a0001c0003t0055g0015a0001c0003t0088g0014 | 3 | HG02717.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.235+3462A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356960 | ||||||
chr2:171356960
|
T | G | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.235+3462A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356960 | ||||||
chr2:171356973
|
A | G | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+3449T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171356973 | ||||||
chr2:171357046
|
G | A | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.235+3376C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171357046 | ||||||
chr2:171357178
|
C | T | 1 | a0001c0001t0004g0250 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.235+3244G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171357178 | ||||||
chr2:171357239
|
G | C | 1 | a0001c0001t0003g0122 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.235+3183C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171357239 | ||||||
chr2:171357557
|
C | T | 1 | a0001c0002t0001g0002 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.235+2865G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171357557 | ||||||
chr2:171357700
|
C | CT | 6 | a0002c0004t0018g0072a0002c0004t0018g0073a0002c0004t0018g0092others(3): Show | 6 | HG01074.hp1 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+2721dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171357700 | ||||||
chr2:171357725
|
C | T | 1 | a0002c0014t0046g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.235+2697G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171357725 | ||||||
chr2:171357788
|
G | A | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG01099.hp1 HG01168.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+2634C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171357788 | ||||||
chr2:171357923
|
T | C | 1 | a0001c0001t0013g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.235+2499A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171357923 | ||||||
chr2:171358003
|
G | A | 328 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(325): Show | 330 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.235+2419C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358003 | ||||||
chr2:171358073
|
A | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+2349T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358073 | ||||||
chr2:171358076
|
T | A | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2346A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358076 | ||||||
chr2:171358109
|
G | T | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2313C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358109 | ||||||
chr2:171358112
|
A | G | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2310T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358112 | ||||||
chr2:171358113
|
G | A | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2309C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358113 | ||||||
chr2:171358114
|
G | A | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2308C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358114 | ||||||
chr2:171358117
|
G | T | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2305C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358117 | ||||||
chr2:171358125
|
C | T | 2 | a0001c0001t0002g0180a0001c0001t0002g0296 | 2 | HG00438.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.235+2297G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358125 | ||||||
chr2:171358156
|
G | A | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2266C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358156 | ||||||
chr2:171358172
|
A | T | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2250T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358172 | ||||||
chr2:171358176
|
C | A | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2246G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358176 | ||||||
chr2:171358177
|
G | C | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2245C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358177 | ||||||
chr2:171358200
|
C | A | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2222G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358200 | ||||||
chr2:171358205
|
G | T | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2217C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358205 | ||||||
chr2:171358208
|
G | A | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2214C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358208 | ||||||
chr2:171358209
|
G | A | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2213C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358209 | ||||||
chr2:171358214
|
G | T | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2208C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358214 | ||||||
chr2:171358220
|
G | T | 1 | a0001c0002t0002g0302 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.235+2202C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358220 | ||||||
chr2:171358306
|
C | G | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+2116G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358306 | ||||||
chr2:171358346
|
G | A | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.235+2076C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358346 | ||||||
chr2:171358353
|
G | GA | 8 | a0001c0001t0001g0135a0001c0001t0001g0197a0001c0001t0004g0242others(5): Show | 8 | HG00738.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+2068dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358353 | ||||||
chr2:171358353
|
GA | G | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+2068delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358353 | ||||||
chr2:171358633
|
T | C | 5 | a0001c0002t0054g0016a0001c0002t0072g0017a0005c0007t0005g0235others(2): Show | 5 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+1789A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358633 | ||||||
chr2:171358711
|
GA | G | 76 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0132others(73): Show | 76 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.235+1710delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358711 | ||||||
chr2:171358717
|
A | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+1705T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358717 | ||||||
chr2:171358769
|
A | G | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.235+1653T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358769 | ||||||
chr2:171358823
|
A | T | 33 | a0001c0001t0074g0090a0001c0002t0002g0302a0001c0002t0007g0298others(30): Show | 33 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.235+1599T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358823 | ||||||
chr2:171358843
|
A | G | 324 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(321): Show | 326 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(323): Show |
intron_variant | MODIFIER | c.235+1579T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358843 | ||||||
chr2:171358976
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.235+1446T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358976 | ||||||
chr2:171358977
|
G | A | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+1445C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171358977 | ||||||
chr2:171359068
|
C | T | 1 | a0001c0001t0003g0117 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.235+1354G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359068 | ||||||
chr2:171359142
|
A | G | 33 | a0001c0001t0029g0252a0001c0002t0029g0056a0001c0002t0054g0016others(30): Show | 33 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.235+1280T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359142 | ||||||
chr2:171359165
|
C | A | 1 | a0001c0003t0019g0024 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.235+1257G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359165 | ||||||
chr2:171359173
|
C | CA | 46 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(43): Show | 47 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.235+1248dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359173 | ||||||
chr2:171359173
|
C | CAA | 34 | a0001c0001t0029g0252a0001c0002t0009g0269a0001c0002t0009g0270others(31): Show | 34 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.235+1247_235+1248d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359173 | ||||||
chr2:171359173
|
CA | C | 7 | a0001c0001t0001g0315a0001c0001t0013g0007a0001c0001t0013g0010others(4): Show | 7 | HG02615.hp2 HG02818.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+1248delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359173 | ||||||
chr2:171359191
|
T | C | 1 | a0001c0001t0017g0053 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.235+1231A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359191 | ||||||
chr2:171359199
|
G | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+1223C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359199 | ||||||
chr2:171359357
|
T | G | 1 | a0001c0002t0001g0224 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.235+1065A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359357 | ||||||
chr2:171359369
|
G | A | 1 | a0001c0001t0071g0088 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.235+1053C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359369 | ||||||
chr2:171359370
|
C | T | 1 | a0001c0001t0071g0088 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.235+1052G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359370 | ||||||
chr2:171359440
|
T | C | 2 | a0001c0001t0002g0214a0001c0001t0002g0215 | 2 | NA19005.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.235+982A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359440 | ||||||
chr2:171359487
|
A | G | 1 | a0008c0010t0032g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.235+935T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359487 | ||||||
chr2:171359548
|
A | G | 19 | a0001c0001t0074g0090a0001c0002t0022g0317a0001c0002t0022g0318others(16): Show | 19 | HG01261.hp1 HG02280.hp2 HG02647.hp2 others(16): Show |
intron_variant | MODIFIER | c.235+874T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359548 | ||||||
chr2:171359618
|
G | A | 2 | a0001c0002t0008g0217a0001c0002t0008g0223 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.235+804C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359618 | ||||||
chr2:171359619
|
G | GT | 36 | a0001c0001t0001g0070a0001c0001t0004g0280a0001c0001t0008g0169others(33): Show | 36 | HG00423.hp1 HG01081.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.235+802dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359619 | ||||||
chr2:171359652
|
C | T | 1 | a0001c0001t0003g0117 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.235+770G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359652 | ||||||
chr2:171359771
|
A | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+651T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359771 | ||||||
chr2:171359842
|
C | T | 18 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(15): Show | 18 | HG01261.hp1 HG02280.hp2 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.235+580G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359842 | ||||||
chr2:171359886
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.235+536C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359886 | ||||||
chr2:171359906
|
A | G | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+516T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 3/9 | chr2 | 171359906 | ||||||
chr2:171360681
|
G | A | 6 | a0001c0002t0033g0324a0001c0002t0033g0330a0001c0002t0089g0325others(3): Show | 6 | HG01261.hp1 HG02895.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-168C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171360681 | ||||||
chr2:171360788
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.144-275C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171360788 | ||||||
chr2:171360813
|
A | ATGGTT | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.144-301_144-300ins others(5): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171360813 | ||||||
chr2:171360844
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.144-331A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171360844 | ||||||
chr2:171360893
|
T | C | 5 | a0001c0005t0015g0099a0001c0005t0015g0100a0001c0005t0015g0101others(2): Show | 5 | HG01074.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.144-380A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171360893 | ||||||
chr2:171361253
|
C | CT | 133 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(130): Show | 134 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.144-741dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171361253 | ||||||
chr2:171361253
|
CT | C | 24 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(21): Show | 24 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.144-741delA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171361253 | ||||||
chr2:171361255
|
T | C | 1 | a0001c0001t0004g0268 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.144-742A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171361255 | ||||||
chr2:171361296
|
T | G | 1 | a0001c0001t0004g0275 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.144-783A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171361296 | ||||||
chr2:171361347
|
C | A | 1 | a0001c0001t0014g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.144-834G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171361347 | ||||||
chr2:171361369
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.144-856A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171361369 | ||||||
chr2:171361551
|
C | T | 3 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292 | 3 | HG00408.hp1 HG02040.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.144-1038G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171361551 | ||||||
chr2:171361835
|
C | A | 1 | a0001c0001t0012g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.144-1322G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171361835 | ||||||
chr2:171361846
|
A | G | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.144-1333T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171361846 | ||||||
chr2:171361935
|
G | A | 2 | a0005c0007t0031g0018a0005c0007t0031g0020 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.144-1422C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171361935 | ||||||
chr2:171362063
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.144-1550T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362063 | ||||||
chr2:171362114
|
C | T | 85 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(82): Show | 86 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.144-1601G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362114 | ||||||
chr2:171362335
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.144-1822C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362335 | ||||||
chr2:171362400
|
A | G | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.144-1887T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362400 | ||||||
chr2:171362497
|
G | A | 1 | a0001c0001t0030g0254 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.144-1984C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362497 | ||||||
chr2:171362542
|
G | A | 2 | a0005c0007t0031g0018a0005c0007t0031g0020 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.144-2029C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362542 | ||||||
chr2:171362566
|
A | AAAAT | 182 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(179): Show | 182 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.144-2057_144-2054d others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362566 | ||||||
chr2:171362566
|
A | AAAATAAA others(1): Show |
30 | a0001c0001t0001g0148a0001c0001t0001g0158a0001c0001t0002g0011others(27): Show | 30 | HG00597.hp2 HG00642.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.144-2061_144-2054d others(10): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362566 | ||||||
chr2:171362566
|
A | AAAATAAA others(5): Show |
4 | a0001c0001t0001g0187a0001c0002t0009g0270a0001c0002t0009g0290others(1): Show | 4 | HG00408.hp1 HG00597.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-2065_144-2054d others(14): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362566 | ||||||
chr2:171362595
|
A | AAATAAAT others(5): Show |
4 | a0001c0002t0054g0016a0005c0007t0005g0235a0005c0007t0031g0018others(1): Show | 4 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-2083_144-2082i others(14): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362595 | ||||||
chr2:171362643
|
A | G | 13 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(10): Show | 13 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.144-2130T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362643 | ||||||
chr2:171362785
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.144-2272A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362785 | ||||||
chr2:171362887
|
G | A | 42 | a0001c0001t0001g0264a0001c0001t0001g0288a0001c0001t0004g0242others(39): Show | 42 | HG01109.hp2 HG01175.hp2 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.144-2374C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362887 | ||||||
chr2:171362949
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.144-2436C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362949 | ||||||
chr2:171362955
|
A | C | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.144-2442T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362955 | ||||||
chr2:171362982
|
T | A | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.144-2469A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171362982 | ||||||
chr2:171363037
|
C | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0067 | 2 | NA18964.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.144-2524G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363037 | ||||||
chr2:171363218
|
A | AT | 8 | a0001c0002t0001g0229a0001c0002t0009g0249a0001c0002t0009g0269others(5): Show | 8 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.144-2706dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363218 | ||||||
chr2:171363288
|
T | C | 1 | a0002c0009t0066g0091 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.144-2775A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363288 | ||||||
chr2:171363573
|
A | C | 18 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(15): Show | 19 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.144-3060T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363573 | ||||||
chr2:171363623
|
T | C | 115 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(112): Show | 115 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.144-3110A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363623 | ||||||
chr2:171363792
|
T | TATATATA others(30): Show |
1 | a0001c0002t0007g0307 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.144-3280_144-3279i others(39): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTA | 57 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0041others(54): Show | 57 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.144-3281_144-3280d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATA | 65 | a0001c0001t0001g0068a0001c0001t0001g0085a0001c0001t0001g0126others(62): Show | 65 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.144-3283_144-3280d others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATATA | 5 | a0001c0001t0001g0039a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.144-3285_144-3280d others(8): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATATAT others(3): Show |
10 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.144-3289_144-3280d others(12): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATATAT others(5): Show |
4 | a0001c0002t0001g0221a0001c0002t0001g0222a0001c0002t0001g0225others(1): Show | 4 | HG02083.hp2 HG02451.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-3291_144-3280d others(14): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATATAT others(7): Show |
2 | a0001c0002t0008g0217a0001c0002t0008g0223 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.144-3293_144-3280d others(16): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATATAT others(11): Show |
3 | a0001c0002t0007g0306a0001c0002t0007g0310a0001c0002t0049g0311 | 3 | HG02027.hp2 HG02080.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.144-3297_144-3280d others(20): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATATAT others(13): Show |
1 | a0004c0008t0001g0300 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.144-3299_144-3280d others(22): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATATAT others(15): Show |
3 | a0001c0002t0007g0313a0001c0002t0027g0304a0001c0002t0027g0305 | 3 | HG01884.hp2 HG03139.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.144-3301_144-3280d others(24): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATATAT others(17): Show |
5 | a0001c0002t0007g0308a0004c0008t0001g0301a0005c0007t0031g0018others(2): Show | 5 | HG01081.hp1 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.144-3280_144-3279i others(26): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATATAT others(19): Show |
4 | a0001c0002t0007g0309a0001c0002t0054g0016a0004c0008t0001g0299others(1): Show | 4 | HG02055.hp1 HG02280.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-3280_144-3279i others(28): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATATAT others(21): Show |
1 | a0001c0002t0072g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.144-3280_144-3279i others(30): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATATAT others(21): Show |
7 | a0001c0002t0035g0326a0001c0002t0035g0327a0002c0004t0018g0072others(4): Show | 7 | HG02280.hp2 HG02717.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.144-3280_144-3279i others(30): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATATAT others(23): Show |
5 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(2): Show | 5 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-3280_144-3279i others(32): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATATAT others(45): Show |
4 | a0001c0002t0033g0324a0001c0002t0033g0330a0001c0002t0090g0323others(1): Show | 4 | HG01261.hp1 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-3280_144-3279i others(54): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATATAT others(47): Show |
1 | a0001c0002t0091g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.144-3280_144-3279i others(56): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
T | TTATATAT others(51): Show |
1 | a0001c0002t0089g0325 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.144-3280_144-3279i others(60): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
TTA | T | 10 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(7): Show | 10 | HG01069.hp1 HG01433.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.144-3281_144-3280d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363792
|
TTATA | T | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.144-3283_144-3280d others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363792 | ||||||
chr2:171363796
|
A | ATATATAT others(41): Show |
1 | a0001c0003t0058g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.144-3284_144-3283i others(50): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363796 | ||||||
chr2:171363796
|
A | ATATATAT others(37): Show |
2 | a0001c0003t0005g0029a0001c0003t0056g0253 | 2 | HG01496.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.144-3284_144-3283i others(46): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363796 | ||||||
chr2:171363796
|
A | ATATATAT others(35): Show |
2 | a0001c0003t0019g0019a0001c0003t0019g0024 | 2 | HG03098.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.144-3284_144-3283i others(44): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363796 | ||||||
chr2:171363796
|
A | ATATATAT others(33): Show |
2 | a0001c0003t0005g0034a0001c0003t0005g0105 | 2 | HG01256.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.144-3284_144-3283i others(42): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363796 | ||||||
chr2:171363796
|
A | ATATATAT others(31): Show |
6 | a0001c0003t0005g0025a0001c0003t0005g0106a0001c0003t0005g0107others(3): Show | 6 | HG00642.hp1 HG00738.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-3284_144-3283i others(40): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363796 | ||||||
chr2:171363796
|
A | ATATATAT others(29): Show |
8 | a0001c0002t0029g0056a0001c0003t0005g0021a0001c0003t0019g0027others(5): Show | 8 | HG00280.hp1 HG01106.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.144-3284_144-3283i others(38): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363796 | ||||||
chr2:171363796
|
A | ATATATAT others(27): Show |
2 | a0001c0003t0005g0022a0001c0003t0005g0023 | 2 | HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.144-3284_144-3283i others(36): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363796 | ||||||
chr2:171363796
|
A | ATATATAT others(25): Show |
1 | a0001c0003t0021g0239 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.144-3284_144-3283i others(34): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363796 | ||||||
chr2:171363796
|
A | ATATATAT others(23): Show |
2 | a0001c0003t0055g0015a0001c0003t0088g0014 | 2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.144-3284_144-3283i others(32): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363796 | ||||||
chr2:171363815
|
T | TATATATA others(18): Show |
3 | a0001c0002t0002g0302a0001c0002t0007g0303a0001c0002t0048g0312 | 3 | HG00423.hp2 NA18969.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.144-3303_144-3302i others(27): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363815 | ||||||
chr2:171363815
|
T | TATATATA others(14): Show |
1 | a0001c0002t0007g0298 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.144-3303_144-3302i others(23): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363815 | ||||||
chr2:171363816
|
C | A | 1 | a0001c0002t0001g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.144-3303G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363816 | ||||||
chr2:171363816
|
C | T | 4 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(1): Show | 4 | HG00423.hp2 NA18941.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-3303G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363816 | ||||||
chr2:171363817
|
T | C | 1 | a0001c0001t0016g0062 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.144-3304A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171363817 | ||||||
chr2:171364183
|
T | C | 7 | a0001c0002t0009g0249a0001c0002t0009g0269a0001c0002t0009g0270others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.144-3670A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171364183 | ||||||
chr2:171364692
|
A | C | 2 | a0001c0001t0003g0093a0001c0001t0003g0125 | 2 | NA18984.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.144-4179T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171364692 | ||||||
chr2:171364708
|
T | C | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.144-4195A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171364708 | ||||||
chr2:171364726
|
G | T | 13 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(10): Show | 13 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.144-4213C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171364726 | ||||||
chr2:171364896
|
G | A | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.144-4383C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171364896 | ||||||
chr2:171365002
|
G | T | 68 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(65): Show | 68 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.144-4489C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171365002 | ||||||
chr2:171365025
|
T | C | 30 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(27): Show | 31 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.144-4512A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171365025 | ||||||
chr2:171365125
|
G | A | 1 | a0007c0013t0082g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.144-4612C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171365125 | ||||||
chr2:171365340
|
T | C | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-4827A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171365340 | ||||||
chr2:171365398
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-4885G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171365398 | ||||||
chr2:171365438
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-4925G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171365438 | ||||||
chr2:171365462
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0020g0112 | 2 | HG00280.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.144-4949A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171365462 | ||||||
chr2:171365470
|
G | A | 1 | a0001c0002t0001g0054 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.144-4957C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171365470 | ||||||
chr2:171365626
|
T | C | 1 | a0001c0001t0002g0172 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.144-5113A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171365626 | ||||||
chr2:171365641
|
T | TAC | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-5130_144-5129d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171365641 | ||||||
chr2:171365753
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-5240C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171365753 | ||||||
chr2:171365777
|
T | A | 1 | a0002c0009t0066g0091 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.144-5264A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171365777 | ||||||
chr2:171365786
|
G | A | 1 | a0001c0001t0004g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.144-5273C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171365786 | ||||||
chr2:171366071
|
G | C | 1 | a0001c0001t0041g0194 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.144-5558C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171366071 | ||||||
chr2:171366123
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG00438.hp2 HG02080.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.144-5610G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171366123 | ||||||
chr2:171366124
|
G | A | 21 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0057others(18): Show | 21 | HG01069.hp1 HG01433.hp1 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.144-5611C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171366124 | ||||||
chr2:171366162
|
G | A | 1 | a0001c0003t0021g0237 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.144-5649C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171366162 | ||||||
chr2:171366174
|
G | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-5661C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171366174 | ||||||
chr2:171366315
|
A | G | 1 | a0001c0002t0001g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.144-5802T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171366315 | ||||||
chr2:171366362
|
T | G | 1 | a0001c0001t0006g0163 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.144-5849A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171366362 | ||||||
chr2:171366452
|
T | C | 116 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(113): Show | 116 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.144-5939A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171366452 | ||||||
chr2:171366809
|
G | A | 1 | a0001c0002t0001g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.144-6296C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171366809 | ||||||
chr2:171366888
|
C | CA | 32 | a0001c0001t0001g0042a0001c0001t0001g0126a0001c0001t0001g0141others(29): Show | 32 | HG00408.hp2 HG00642.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.144-6376dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171366888 | ||||||
chr2:171367096
|
A | G | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.144-6583T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171367096 | ||||||
chr2:171367113
|
A | G | 3 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0120 | 3 | HG01192.hp1 HG01346.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.144-6600T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171367113 | ||||||
chr2:171367320
|
T | C | 1 | a0007c0013t0082g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.144-6807A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171367320 | ||||||
chr2:171367366
|
AAGGAGAT others(6): Show |
A | 4 | a0001c0005t0015g0099a0001c0005t0015g0100a0001c0005t0015g0101others(1): Show | 4 | HG02055.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-6866_144-6854d others(15): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171367366 | ||||||
chr2:171367381
|
CAG | C | 4 | a0001c0005t0015g0099a0001c0005t0015g0100a0001c0005t0015g0101others(1): Show | 4 | HG02055.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-6870_144-6869d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171367381 | ||||||
chr2:171367561
|
C | T | 2 | a0005c0007t0031g0018a0005c0007t0031g0020 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.144-7048G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171367561 | ||||||
chr2:171367593
|
G | A | 1 | a0001c0001t0010g0265 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.144-7080C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171367593 | ||||||
chr2:171367713
|
C | T | 323 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(320): Show | 325 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(322): Show |
intron_variant | MODIFIER | c.144-7200G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171367713 | ||||||
chr2:171367888
|
T | A | 1 | a0001c0001t0003g0079 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.144-7375A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171367888 | ||||||
chr2:171367919
|
G | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-7406C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171367919 | ||||||
chr2:171368064
|
C | T | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.144-7551G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171368064 | ||||||
chr2:171368120
|
A | G | 1 | a0001c0003t0005g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.144-7607T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171368120 | ||||||
chr2:171368129
|
A | T | 6 | a0001c0002t0033g0324a0001c0002t0033g0330a0001c0002t0089g0325others(3): Show | 6 | HG01261.hp1 HG02895.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-7616T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171368129 | ||||||
chr2:171368155
|
C | G | 88 | a0001c0001t0001g0111a0001c0001t0001g0264a0001c0001t0001g0288others(85): Show | 89 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.144-7642G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171368155 | ||||||
chr2:171368250
|
A | T | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.144-7737T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171368250 | ||||||
chr2:171368265
|
C | T | 1 | a0007c0013t0082g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.144-7752G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171368265 | ||||||
chr2:171368280
|
G | T | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.144-7767C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171368280 | ||||||
chr2:171368325
|
A | G | 2 | a0005c0007t0031g0018a0005c0007t0031g0020 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.144-7812T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171368325 | ||||||
chr2:171368784
|
C | T | 1 | a0001c0001t0011g0260 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.144-8271G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171368784 | ||||||
chr2:171368878
|
T | A | 2 | a0001c0003t0021g0237a0001c0003t0085g0238 | 2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.144-8365A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171368878 | ||||||
chr2:171368988
|
C | A | 1 | a0001c0002t0001g0054 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.144-8475G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171368988 | ||||||
chr2:171369018
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.144-8505G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171369018 | ||||||
chr2:171369026
|
C | T | 51 | a0001c0001t0001g0086a0001c0001t0001g0128a0001c0001t0001g0160others(48): Show | 51 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.144-8513G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171369026 | ||||||
chr2:171369076
|
T | TA | 51 | a0001c0001t0029g0252a0001c0002t0022g0317a0001c0002t0022g0318others(48): Show | 51 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.144-8564dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171369076 | ||||||
chr2:171369163
|
G | A | 3 | a0001c0001t0006g0163a0001c0001t0006g0165a0001c0001t0006g0199 | 3 | NA18969.hp1 NA18979.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.144-8650C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171369163 | ||||||
chr2:171369238
|
G | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-8725C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171369238 | ||||||
chr2:171369254
|
C | T | 1 | a0001c0001t0017g0204 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.144-8741G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171369254 | ||||||
chr2:171369322
|
C | A | 1 | a0001c0001t0006g0184 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.144-8809G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171369322 | ||||||
chr2:171369602
|
A | G | 1 | a0007c0013t0082g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.144-9089T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171369602 | ||||||
chr2:171369641
|
G | A | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.144-9128C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171369641 | ||||||
chr2:171369822
|
T | C | 2 | a0001c0002t0027g0304a0001c0002t0027g0305 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.144-9309A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171369822 | ||||||
chr2:171369832
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.144-9319G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171369832 | ||||||
chr2:171369833
|
C | G | 76 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0132others(73): Show | 76 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.144-9320G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171369833 | ||||||
chr2:171369869
|
C | G | 1 | a0001c0003t0086g0028 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.144-9356G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171369869 | ||||||
chr2:171369895
|
G | A | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.144-9382C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171369895 | ||||||
chr2:171370026
|
A | T | 1 | a0001c0001t0001g0213 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.144-9513T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370026 | ||||||
chr2:171370089
|
T | C | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.144-9576A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370089 | ||||||
chr2:171370123
|
A | G | 8 | a0001c0001t0074g0090a0002c0004t0018g0072a0002c0004t0018g0073others(5): Show | 8 | HG01074.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.144-9610T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370123 | ||||||
chr2:171370211
|
T | C | 32 | a0001c0001t0029g0252a0001c0002t0029g0056a0001c0002t0054g0016others(29): Show | 32 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.144-9698A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370211 | ||||||
chr2:171370244
|
A | G | 45 | a0001c0001t0029g0252a0001c0002t0022g0317a0001c0002t0022g0318others(42): Show | 45 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.144-9731T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370244 | ||||||
chr2:171370358
|
G | A | 7 | a0001c0001t0011g0202a0001c0001t0011g0255a0001c0001t0011g0258others(4): Show | 7 | HG01934.hp2 HG01952.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.144-9845C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370358 | ||||||
chr2:171370518
|
A | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-10005T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370518 | ||||||
chr2:171370521
|
G | A | 1 | a0001c0002t0001g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.144-10008C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370521 | ||||||
chr2:171370557
|
C | T | 5 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0135others(2): Show | 5 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.144-10044G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370557 | ||||||
chr2:171370694
|
G | A | 1 | a0005c0007t0031g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.144-10181C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370694 | ||||||
chr2:171370716
|
G | A | 2 | a0001c0002t0035g0326a0001c0002t0035g0327 | 2 | HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.144-10203C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370716 | ||||||
chr2:171370770
|
A | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-10257T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370770 | ||||||
chr2:171370777
|
T | G | 4 | a0001c0005t0015g0099a0001c0005t0015g0100a0001c0005t0015g0101others(1): Show | 4 | HG02055.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-10264A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370777 | ||||||
chr2:171370786
|
G | A | 1 | a0001c0002t0007g0309 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.144-10273C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370786 | ||||||
chr2:171370873
|
A | G | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.144-10360T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370873 | ||||||
chr2:171370943
|
G | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-10430C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370943 | ||||||
chr2:171370977
|
T | A | 1 | a0001c0001t0001g0038 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.144-10464A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171370977 | ||||||
chr2:171371070
|
A | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-10557T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371070 | ||||||
chr2:171371128
|
A | C | 1 | a0001c0001t0001g0147 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.144-10615T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371128 | ||||||
chr2:171371332
|
A | AGTTTTT | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-10825_144-1082 others(10): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371332 | ||||||
chr2:171371443
|
G | A | 33 | a0001c0001t0001g0111a0001c0001t0003g0001a0001c0001t0003g0075others(30): Show | 34 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.144-10930C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371443 | ||||||
chr2:171371461
|
A | G | 2 | a0001c0003t0025g0030a0001c0003t0083g0032 | 2 | HG00280.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.144-10948T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371461 | ||||||
chr2:171371523
|
A | T | 1 | a0001c0001t0001g0187 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.144-11010T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371523 | ||||||
chr2:171371830
|
T | TTATTAC | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-11323_144-1131 others(10): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371830 | ||||||
chr2:171371836
|
C | CTAT | 48 | a0001c0001t0001g0085a0001c0001t0001g0142a0001c0001t0001g0146others(45): Show | 48 | HG00621.hp1 HG01081.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.144-11326_144-1132 others(7): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371836 | ||||||
chr2:171371836
|
C | CTATTAT | 33 | a0001c0001t0001g0145a0001c0001t0012g0123a0001c0001t0074g0090others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.144-11329_144-1132 others(10): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371836 | ||||||
chr2:171371836
|
C | CTATTATT others(2): Show |
10 | a0001c0001t0001g0144a0001c0001t0012g0050a0001c0001t0012g0051others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.144-11332_144-1132 others(13): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371836 | ||||||
chr2:171371836
|
C | CTATTATT others(5): Show |
4 | a0001c0001t0012g0049a0001c0002t0001g0054a0001c0002t0035g0327others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-11335_144-1132 others(16): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371836 | ||||||
chr2:171371836
|
C | CTATTATT others(8): Show |
1 | a0001c0002t0093g0322 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.144-11338_144-1132 others(19): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371836 | ||||||
chr2:171371836
|
CTAT | C | 47 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(44): Show | 47 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-11326_144-1132 others(7): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371836 | ||||||
chr2:171371836
|
CTATTAT | C | 111 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0094others(108): Show | 112 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.144-11329_144-1132 others(10): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371836 | ||||||
chr2:171371836
|
CTATTATT others(2): Show |
C | 5 | a0001c0005t0015g0099a0001c0005t0015g0100a0001c0005t0015g0101others(2): Show | 5 | HG01074.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.144-11332_144-1132 others(13): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371836 | ||||||
chr2:171371884
|
T | C | 2 | a0001c0001t0001g0140a0001c0001t0063g0139 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.144-11371A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371884 | ||||||
chr2:171371954
|
G | A | 1 | a0001c0001t0012g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.144-11441C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171371954 | ||||||
chr2:171372007
|
T | C | 3 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320 | 3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.144-11494A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171372007 | ||||||
chr2:171372158
|
C | A | 1 | a0001c0003t0005g0021 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.144-11645G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171372158 | ||||||
chr2:171372233
|
G | T | 31 | a0001c0001t0029g0252a0001c0002t0054g0016a0001c0002t0072g0017others(28): Show | 31 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.144-11720C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171372233 | ||||||
chr2:171372298
|
T | A | 31 | a0001c0001t0029g0252a0001c0002t0054g0016a0001c0002t0072g0017others(28): Show | 31 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.144-11785A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171372298 | ||||||
chr2:171372359
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-11846G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171372359 | ||||||
chr2:171372427
|
A | C | 2 | a0001c0003t0005g0025a0001c0003t0005g0029 | 2 | HG01496.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.144-11914T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171372427 | ||||||
chr2:171372560
|
C | T | 2 | a0001c0002t0001g0226a0001c0002t0001g0230 | 2 | HG02083.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.144-12047G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171372560 | ||||||
chr2:171372561
|
G | A | 1 | a0001c0001t0013g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.144-12048C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171372561 | ||||||
chr2:171372572
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.144-12059C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171372572 | ||||||
chr2:171372688
|
A | G | 1 | a0001c0001t0002g0195 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.144-12175T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171372688 | ||||||
chr2:171372739
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.144-12226A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171372739 | ||||||
chr2:171373058
|
T | C | 1 | a0001c0001t0050g0208 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.144-12545A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373058 | ||||||
chr2:171373060
|
C | G | 2 | a0001c0001t0017g0212a0001c0001t0051g0211 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.144-12547G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373060 | ||||||
chr2:171373264
|
C | T | 1 | a0001c0001t0004g0263 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.144-12751G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373264 | ||||||
chr2:171373477
|
T | C | 1 | a0001c0001t0003g0125 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.144-12964A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373477 | ||||||
chr2:171373505
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-12992G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373505 | ||||||
chr2:171373584
|
G | T | 112 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(109): Show | 112 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.144-13071C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373584 | ||||||
chr2:171373592
|
T | C | 5 | a0001c0005t0015g0099a0001c0005t0015g0100a0001c0005t0015g0101others(2): Show | 5 | HG01074.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.144-13079A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373592 | ||||||
chr2:171373649
|
T | A | 1 | a0001c0002t0007g0307 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.144-13136A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373649 | ||||||
chr2:171373669
|
G | A | 46 | a0001c0001t0001g0264a0001c0001t0001g0288a0001c0001t0002g0214others(43): Show | 46 | HG00597.hp1 HG01109.hp2 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.144-13156C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373669 | ||||||
chr2:171373683
|
T | C | 1 | a0002c0014t0046g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.144-13170A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373683 | ||||||
chr2:171373686
|
G | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-13173C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373686 | ||||||
chr2:171373727
|
T | G | 2 | a0001c0003t0005g0105a0001c0003t0005g0106 | 2 | HG00642.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.144-13214A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373727 | ||||||
chr2:171373788
|
G | A | 1 | a0001c0001t0004g0250 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.144-13275C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373788 | ||||||
chr2:171373924
|
G | C | 3 | a0001c0001t0004g0250a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | NA18948.hp2 NA19060.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.144-13411C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373924 | ||||||
chr2:171373948
|
G | A | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.144-13435C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373948 | ||||||
chr2:171373993
|
G | A | 1 | a0002c0004t0018g0072 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.144-13480C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171373993 | ||||||
chr2:171374028
|
C | T | 324 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(321): Show | 326 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(323): Show |
intron_variant | MODIFIER | c.144-13515G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171374028 | ||||||
chr2:171374053
|
C | T | 31 | a0001c0001t0029g0252a0001c0002t0054g0016a0001c0002t0072g0017others(28): Show | 31 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.144-13540G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171374053 | ||||||
chr2:171374293
|
T | C | 1 | a0001c0002t0007g0313 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.144-13780A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171374293 | ||||||
chr2:171374339
|
GA | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-13827delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171374339 | ||||||
chr2:171374408
|
G | C | 18 | a0001c0001t0004g0281a0001c0002t0001g0002a0001c0002t0001g0044others(15): Show | 19 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.144-13895C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171374408 | ||||||
chr2:171374468
|
G | A | 31 | a0001c0001t0029g0252a0001c0002t0054g0016a0001c0002t0072g0017others(28): Show | 31 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.144-13955C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171374468 | ||||||
chr2:171374544
|
A | C | 1 | a0001c0001t0080g0284 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.144-14031T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171374544 | ||||||
chr2:171374581
|
G | A | 2 | a0005c0007t0031g0018a0005c0007t0031g0020 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.144-14068C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171374581 | ||||||
chr2:171374851
|
C | CT | 7 | a0001c0002t0001g0221a0001c0002t0001g0222a0002c0004t0018g0072others(4): Show | 7 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.144-14339dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171374851 | ||||||
chr2:171375078
|
C | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-14565G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171375078 | ||||||
chr2:171375214
|
C | T | 2 | a0002c0004t0018g0072a0002c0004t0018g0073 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.144-14701G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171375214 | ||||||
chr2:171375233
|
C | T | 1 | a0001c0001t0023g0179 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144-14720G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171375233 | ||||||
chr2:171375235
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.144-14722G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171375235 | ||||||
chr2:171375508
|
A | G | 2 | a0001c0001t0040g0198a0001c0001t0041g0194 | 2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.144-14995T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171375508 | ||||||
chr2:171375549
|
G | T | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.144-15036C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171375549 | ||||||
chr2:171375674
|
T | A | 1 | a0001c0001t0073g0063 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.144-15161A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171375674 | ||||||
chr2:171375782
|
A | C | 5 | a0001c0001t0002g0087a0001c0001t0002g0178a0001c0001t0002g0180others(2): Show | 5 | HG00438.hp1 HG00558.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-15269T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171375782 | ||||||
chr2:171375809
|
A | C | 111 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(108): Show | 111 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.144-15296T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171375809 | ||||||
chr2:171375855
|
T | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-15342A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171375855 | ||||||
chr2:171375884
|
A | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-15371T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171375884 | ||||||
chr2:171375904
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.144-15391A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171375904 | ||||||
chr2:171376071
|
T | A | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.144-15558A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171376071 | ||||||
chr2:171376142
|
C | A | 15 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(12): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.144-15629G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171376142 | ||||||
chr2:171376147
|
C | T | 15 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(12): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.144-15634G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171376147 | ||||||
chr2:171376163
|
A | G | 2 | a0001c0003t0005g0025a0001c0003t0005g0029 | 2 | HG01496.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.144-15650T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171376163 | ||||||
chr2:171376284
|
T | G | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.143+15759A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171376284 | ||||||
chr2:171376362
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+15681G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171376362 | ||||||
chr2:171376809
|
T | C | 2 | a0001c0001t0001g0256a0001c0001t0067g0243 | 2 | NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.143+15234A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171376809 | ||||||
chr2:171376902
|
G | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+15141C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171376902 | ||||||
chr2:171377352
|
A | AAAAAT | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+14686_143+1469 others(9): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171377352 | ||||||
chr2:171377524
|
C | T | 35 | a0001c0001t0029g0252a0001c0002t0054g0016a0001c0002t0072g0017others(32): Show | 35 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.143+14519G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171377524 | ||||||
chr2:171377851
|
C | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+14192G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171377851 | ||||||
chr2:171377939
|
A | T | 1 | a0001c0001t0001g0143 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.143+14104T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171377939 | ||||||
chr2:171377942
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+14101G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171377942 | ||||||
chr2:171378218
|
C | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0013g0009others(2): Show | 5 | HG02615.hp2 HG02896.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.143+13825G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171378218 | ||||||
chr2:171378280
|
T | C | 2 | a0001c0001t0010g0265a0001c0001t0030g0254 | 2 | HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.143+13763A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171378280 | ||||||
chr2:171378460
|
C | T | 2 | a0001c0001t0003g0075a0001c0001t0003g0232 | 2 | NA18966.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.143+13583G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171378460 | ||||||
chr2:171378556
|
C | T | 32 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(29): Show | 33 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.143+13487G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171378556 | ||||||
chr2:171378575
|
T | G | 2 | a0001c0002t0027g0304a0001c0002t0027g0305 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.143+13468A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171378575 | ||||||
chr2:171378627
|
T | C | 1 | a0007c0013t0082g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.143+13416A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171378627 | ||||||
chr2:171379038
|
T | C | 1 | a0001c0001t0002g0161 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.143+13005A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171379038 | ||||||
chr2:171379201
|
T | C | 2 | a0001c0003t0055g0015a0001c0003t0088g0014 | 2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.143+12842A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171379201 | ||||||
chr2:171379443
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+12600G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171379443 | ||||||
chr2:171379447
|
T | TA | 8 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(5): Show | 8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.143+12595dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171379447 | ||||||
chr2:171379447
|
TA | T | 44 | a0001c0001t0001g0111a0001c0001t0001g0197a0001c0001t0003g0115others(41): Show | 45 | HG00280.hp2 HG00423.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.143+12595delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171379447 | ||||||
chr2:171379522
|
T | TA | 19 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(16): Show | 19 | HG01069.hp1 HG01109.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.143+12520dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171379522 | ||||||
chr2:171379702
|
G | A | 2 | a0001c0002t0008g0217a0001c0002t0008g0223 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.143+12341C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171379702 | ||||||
chr2:171379864
|
T | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+12179A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171379864 | ||||||
chr2:171379897
|
T | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+12146A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171379897 | ||||||
chr2:171380177
|
G | C | 1 | a0001c0001t0069g0248 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.143+11866C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171380177 | ||||||
chr2:171380178
|
GC | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+11864delG | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171380178 | ||||||
chr2:171380231
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+11812G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171380231 | ||||||
chr2:171380422
|
T | A | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.143+11621A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171380422 | ||||||
chr2:171380445
|
G | C | 1 | a0001c0002t0009g0269 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.143+11598C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171380445 | ||||||
chr2:171380452
|
C | A | 2 | a0001c0001t0074g0090a0002c0014t0046g0089 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.143+11591G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171380452 | ||||||
chr2:171380654
|
A | G | 1 | a0001c0001t0002g0185 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.143+11389T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171380654 | ||||||
chr2:171380758
|
C | G | 38 | a0001c0001t0001g0213a0001c0001t0029g0252a0001c0001t0064g0210others(35): Show | 38 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.143+11285G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171380758 | ||||||
chr2:171380962
|
T | C | 208 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(205): Show | 209 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.143+11081A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171380962 | ||||||
chr2:171380992
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.143+11051G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171380992 | ||||||
chr2:171381052
|
T | C | 1 | a0001c0002t0001g0226 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.143+10991A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381052 | ||||||
chr2:171381079
|
C | T | 1 | a0001c0001t0050g0208 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.143+10964G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381079 | ||||||
chr2:171381096
|
A | G | 1 | a0001c0001t0008g0047 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.143+10947T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381096 | ||||||
chr2:171381102
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.143+10941G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381102 | ||||||
chr2:171381157
|
G | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+10886C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381157 | ||||||
chr2:171381218
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.143+10825T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381218 | ||||||
chr2:171381241
|
A | G | 1 | a0001c0002t0033g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.143+10802T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381241 | ||||||
chr2:171381358
|
C | T | 1 | a0001c0001t0003g0001 | 2 | NA19066.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.143+10685G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381358 | ||||||
chr2:171381449
|
T | G | 12 | a0001c0001t0029g0252a0001c0003t0005g0025a0001c0003t0005g0029others(9): Show | 12 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.143+10594A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381449 | ||||||
chr2:171381522
|
A | T | 1 | a0001c0001t0004g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.143+10521T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381522 | ||||||
chr2:171381561
|
A | T | 1 | a0001c0002t0057g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.143+10482T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381561 | ||||||
chr2:171381677
|
T | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.143+10366A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381677 | ||||||
chr2:171381711
|
G | A | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.143+10332C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381711 | ||||||
chr2:171381718
|
G | A | 10 | a0001c0001t0074g0090a0001c0002t0009g0290a0001c0002t0009g0291others(7): Show | 10 | HG00408.hp1 HG01074.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.143+10325C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381718 | ||||||
chr2:171381780
|
C | CT | 39 | a0001c0001t0001g0039a0001c0001t0001g0070a0001c0001t0001g0156others(36): Show | 39 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.143+10262dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381780 | ||||||
chr2:171381780
|
CT | C | 43 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(40): Show | 43 | HG00280.hp1 HG00408.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.143+10262delA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381780 | ||||||
chr2:171381815
|
C | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+10228G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381815 | ||||||
chr2:171381923
|
A | G | 32 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0029g0252others(29): Show | 32 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.143+10120T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381923 | ||||||
chr2:171381932
|
T | A | 31 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0029g0252others(28): Show | 31 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.143+10111A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381932 | ||||||
chr2:171381972
|
C | T | 1 | a0001c0001t0012g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143+10071G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171381972 | ||||||
chr2:171382024
|
C | T | 10 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0140others(7): Show | 10 | HG00738.hp2 HG01074.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.143+10019G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171382024 | ||||||
chr2:171382046
|
T | G | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.143+9997A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171382046 | ||||||
chr2:171382071
|
C | T | 76 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0029g0252others(73): Show | 77 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.143+9972G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171382071 | ||||||
chr2:171382108
|
C | A | 20 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(17): Show | 21 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.143+9935G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171382108 | ||||||
chr2:171382262
|
T | C | 1 | a0001c0002t0001g0002 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.143+9781A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171382262 | ||||||
chr2:171382448
|
G | A | 4 | a0001c0005t0015g0099a0001c0005t0015g0100a0001c0005t0015g0101others(1): Show | 4 | HG02055.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+9595C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171382448 | ||||||
chr2:171382528
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.143+9515C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171382528 | ||||||
chr2:171382762
|
A | C | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+9281T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171382762 | ||||||
chr2:171382774
|
C | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0189 | 2 | NA18994.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.143+9269G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171382774 | ||||||
chr2:171382793
|
C | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+9250G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171382793 | ||||||
chr2:171382816
|
T | C | 1 | a0001c0001t0001g0170 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.143+9227A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171382816 | ||||||
chr2:171382887
|
A | G | 19 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(16): Show | 19 | HG01074.hp1 HG01261.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.143+9156T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171382887 | ||||||
chr2:171383052
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.143+8991G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171383052 | ||||||
chr2:171383118
|
A | C | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.143+8925T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171383118 | ||||||
chr2:171383249
|
G | A | 111 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0057others(108): Show | 112 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.143+8794C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171383249 | ||||||
chr2:171383313
|
T | G | 2 | a0001c0001t0053g0244a0001c0001t0069g0248 | 2 | HG01109.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.143+8730A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171383313 | ||||||
chr2:171383431
|
G | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+8612C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171383431 | ||||||
chr2:171383651
|
T | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+8392A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171383651 | ||||||
chr2:171383653
|
A | C | 22 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0057others(19): Show | 22 | HG01069.hp1 HG01109.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.143+8390T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171383653 | ||||||
chr2:171383789
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0008g0046 | 2 | NA18951.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.143+8254G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171383789 | ||||||
chr2:171384010
|
A | G | 1 | a0001c0002t0001g0222 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.143+8033T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171384010 | ||||||
chr2:171384269
|
A | C | 4 | a0001c0001t0016g0061a0001c0001t0016g0062a0001c0001t0016g0064others(1): Show | 4 | NA18952.hp2 NA18953.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+7774T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171384269 | ||||||
chr2:171384608
|
C | T | 323 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(320): Show | 325 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(322): Show |
intron_variant | MODIFIER | c.143+7435G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171384608 | ||||||
chr2:171384691
|
T | C | 2 | a0005c0007t0005g0235a0007c0013t0082g0297 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.143+7352A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171384691 | ||||||
chr2:171384969
|
AT | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+7073delA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171384969 | ||||||
chr2:171384992
|
A | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.143+7051T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171384992 | ||||||
chr2:171385019
|
C | A | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.143+7024G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171385019 | ||||||
chr2:171385058
|
T | C | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.143+6985A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171385058 | ||||||
chr2:171385270
|
A | G | 2 | a0001c0001t0002g0214a0001c0001t0002g0215 | 2 | NA19005.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.143+6773T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171385270 | ||||||
chr2:171385334
|
C | A | 1 | a0001c0001t0001g0315 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.143+6709G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171385334 | ||||||
chr2:171385335
|
T | A | 1 | a0001c0001t0001g0315 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.143+6708A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171385335 | ||||||
chr2:171385336
|
C | A | 1 | a0001c0001t0001g0315 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.143+6707G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171385336 | ||||||
chr2:171385336
|
C | CA | 6 | a0001c0001t0001g0170a0001c0001t0043g0171a0001c0002t0009g0290others(3): Show | 6 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.143+6706dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171385336 | ||||||
chr2:171385336
|
CA | C | 16 | a0001c0001t0002g0296a0001c0002t0022g0317a0001c0002t0022g0318others(13): Show | 16 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(13): Show |
intron_variant | MODIFIER | c.143+6706delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171385336 | ||||||
chr2:171385469
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.143+6574C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171385469 | ||||||
chr2:171385620
|
A | G | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.143+6423T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171385620 | ||||||
chr2:171385669
|
T | C | 319 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(316): Show | 321 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.143+6374A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171385669 | ||||||
chr2:171386245
|
G | C | 2 | a0001c0003t0055g0015a0001c0003t0088g0014 | 2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.143+5798C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171386245 | ||||||
chr2:171386470
|
A | G | 4 | a0001c0001t0004g0242a0001c0001t0004g0282a0001c0001t0004g0289others(1): Show | 4 | HG02602.hp1 NA18948.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+5573T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171386470 | ||||||
chr2:171386598
|
T | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.143+5445A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171386598 | ||||||
chr2:171387034
|
A | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+5009T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387034 | ||||||
chr2:171387096
|
T | C | 56 | a0001c0001t0001g0256a0001c0001t0001g0264a0001c0001t0001g0288others(53): Show | 56 | HG00597.hp1 HG01109.hp2 HG01175.hp2 others(53): Show |
intron_variant | MODIFIER | c.143+4947A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387096 | ||||||
chr2:171387127
|
A | AGCCT | 328 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(325): Show | 330 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.143+4915_143+4916i others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387127 | ||||||
chr2:171387212
|
C | T | 1 | a0001c0001t0008g0046 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.143+4831G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387212 | ||||||
chr2:171387239
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.143+4804T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387239 | ||||||
chr2:171387274
|
G | A | 2 | a0001c0002t0001g0218a0001c0002t0057g0220 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.143+4769C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387274 | ||||||
chr2:171387331
|
A | G | 1 | a0001c0001t0006g0199 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.143+4712T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387331 | ||||||
chr2:171387516
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+4527G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387516 | ||||||
chr2:171387541
|
AT | A | 19 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(16): Show | 19 | HG00423.hp2 HG01081.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.143+4501delA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387541 | ||||||
chr2:171387543
|
T | A | 56 | a0001c0001t0029g0252a0001c0002t0001g0002a0001c0002t0001g0044others(53): Show | 57 | HG00280.hp1 HG00408.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.143+4500A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387543 | ||||||
chr2:171387543
|
T | TA | 18 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(15): Show | 18 | HG01261.hp1 HG02280.hp2 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.143+4499dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387543 | ||||||
chr2:171387554
|
T | A | 20 | a0001c0001t0002g0201a0001c0001t0012g0236a0001c0001t0044g0162others(17): Show | 20 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.143+4489A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387554 | ||||||
chr2:171387555
|
T | A | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.143+4488A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387555 | ||||||
chr2:171387557
|
T | C | 41 | a0001c0001t0029g0252a0001c0002t0001g0227a0001c0002t0001g0229others(38): Show | 41 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.143+4486A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387557 | ||||||
chr2:171387562
|
T | A | 1 | a0001c0001t0020g0274 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.143+4481A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387562 | ||||||
chr2:171387611
|
T | C | 1 | a0001c0003t0019g0019 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.143+4432A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387611 | ||||||
chr2:171387664
|
G | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.143+4379C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387664 | ||||||
chr2:171387679
|
T | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+4364A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387679 | ||||||
chr2:171387734
|
T | C | 1 | a0001c0001t0041g0194 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.143+4309A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387734 | ||||||
chr2:171387802
|
T | TA | 4 | a0001c0001t0016g0061a0001c0001t0016g0062a0001c0001t0016g0064others(1): Show | 4 | NA18952.hp2 NA18953.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+4240dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387802 | ||||||
chr2:171387883
|
C | T | 36 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0132others(33): Show | 36 | HG00609.hp2 HG00642.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.143+4160G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171387883 | ||||||
chr2:171388291
|
C | T | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.143+3752G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171388291 | ||||||
chr2:171388304
|
A | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+3739T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171388304 | ||||||
chr2:171388328
|
A | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+3715T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171388328 | ||||||
chr2:171388343
|
C | T | 15 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(12): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.143+3700G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171388343 | ||||||
chr2:171388397
|
T | C | 18 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(15): Show | 18 | HG01261.hp1 HG02280.hp2 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.143+3646A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171388397 | ||||||
chr2:171388494
|
A | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.143+3549T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171388494 | ||||||
chr2:171388501
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.143+3542G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171388501 | ||||||
chr2:171388567
|
G | T | 18 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(15): Show | 18 | HG01261.hp1 HG02280.hp2 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.143+3476C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171388567 | ||||||
chr2:171388597
|
C | T | 4 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(1): Show | 4 | HG00423.hp2 NA18941.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+3446G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171388597 | ||||||
chr2:171389013
|
C | T | 4 | a0001c0001t0012g0049a0001c0001t0012g0050a0001c0001t0012g0051others(1): Show | 4 | HG02145.hp1 HG02622.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+3030G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171389013 | ||||||
chr2:171389340
|
T | C | 2 | a0001c0001t0024g0102a0001c0001t0024g0207 | 2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.143+2703A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171389340 | ||||||
chr2:171389425
|
C | G | 5 | a0001c0001t0074g0090a0002c0004t0018g0072a0002c0004t0018g0073others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.143+2618G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171389425 | ||||||
chr2:171389453
|
T | C | 1 | a0001c0001t0028g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.143+2590A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171389453 | ||||||
chr2:171389514
|
C | CA | 15 | a0001c0001t0001g0264a0001c0001t0002g0177a0001c0001t0003g0076others(12): Show | 15 | HG01074.hp1 HG01106.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.143+2528dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171389514 | ||||||
chr2:171389514
|
CA | C | 107 | a0001c0001t0001g0038a0001c0001t0001g0055a0001c0001t0001g0058others(104): Show | 108 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.143+2528delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171389514 | ||||||
chr2:171389514
|
CAA | C | 92 | a0001c0001t0001g0039a0001c0001t0001g0059a0001c0001t0001g0067others(89): Show | 92 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.143+2527_143+2528d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171389514 | ||||||
chr2:171389514
|
CAAA | C | 14 | a0001c0001t0001g0132a0001c0002t0022g0317a0001c0002t0022g0318others(11): Show | 14 | HG01169.hp1 HG01261.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.143+2526_143+2528d others(5): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171389514 | ||||||
chr2:171389578
|
T | C | 1 | a0001c0001t0068g0026 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.143+2465A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171389578 | ||||||
chr2:171389582
|
A | T | 1 | a0001c0002t0091g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.143+2461T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171389582 | ||||||
chr2:171389890
|
T | TA | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.143+2152dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171389890 | ||||||
chr2:171390036
|
T | C | 1 | a0001c0001t0050g0208 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.143+2007A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171390036 | ||||||
chr2:171390162
|
A | G | 1 | a0001c0003t0021g0239 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.143+1881T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171390162 | ||||||
chr2:171390290
|
G | C | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+1753C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171390290 | ||||||
chr2:171390387
|
A | T | 1 | a0001c0001t0001g0156 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.143+1656T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171390387 | ||||||
chr2:171390405
|
G | A | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.143+1638C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171390405 | ||||||
chr2:171390405
|
G | C | 4 | a0001c0002t0001g0224a0001c0002t0001g0225a0001c0002t0001g0226others(1): Show | 4 | HG02056.hp1 HG02083.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+1638C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171390405 | ||||||
chr2:171390771
|
T | C | 329 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(326): Show | 331 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(328): Show |
intron_variant | MODIFIER | c.143+1272A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171390771 | ||||||
chr2:171390794
|
T | C | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.143+1249A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171390794 | ||||||
chr2:171390848
|
C | T | 1 | a0001c0001t0003g0082 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.143+1195G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171390848 | ||||||
chr2:171391180
|
C | T | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.143+863G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171391180 | ||||||
chr2:171391302
|
T | C | 1 | a0001c0003t0019g0024 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.143+741A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171391302 | ||||||
chr2:171391679
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+364G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171391679 | ||||||
chr2:171391735
|
C | A | 5 | a0001c0005t0015g0099a0001c0005t0015g0100a0001c0005t0015g0101others(2): Show | 5 | HG01074.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.143+308G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171391735 | ||||||
chr2:171391763
|
G | A | 4 | a0001c0003t0021g0237a0001c0003t0021g0239a0001c0003t0021g0240others(1): Show | 4 | HG02258.hp1 HG02559.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+280C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171391763 | ||||||
chr2:171391944
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+99G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 2/9 | chr2 | 171391944 | ||||||
chr2:171392487
|
G | A | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12-290C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171392487 | ||||||
chr2:171392523
|
A | AT | 5 | a0001c0001t0024g0102a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG02040.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-327dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171392523 | ||||||
chr2:171392694
|
A | C | 1 | a0001c0001t0004g0250 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-12-497T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171392694 | ||||||
chr2:171392806
|
T | G | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-12-609A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171392806 | ||||||
chr2:171392895
|
G | A | 15 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(12): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12-698C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171392895 | ||||||
chr2:171392942
|
C | CA | 38 | a0001c0001t0002g0177a0001c0001t0004g0275a0001c0001t0011g0202others(35): Show | 38 | HG00280.hp1 HG00408.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12-746dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171392942 | ||||||
chr2:171392942
|
CA | C | 25 | a0001c0001t0077g0116a0001c0002t0022g0317a0001c0002t0022g0318others(22): Show | 25 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-12-746delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171392942 | ||||||
chr2:171393033
|
G | T | 1 | a0001c0001t0003g0295 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-12-836C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171393033 | ||||||
chr2:171393074
|
C | T | 114 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(111): Show | 114 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-12-877G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171393074 | ||||||
chr2:171393075
|
G | A | 1 | a0001c0002t0027g0305 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-12-878C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171393075 | ||||||
chr2:171393123
|
A | G | 26 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(23): Show | 27 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-12-926T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171393123 | ||||||
chr2:171393310
|
G | A | 2 | a0001c0001t0003g0093a0001c0001t0003g0125 | 2 | NA18984.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-12-1113C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171393310 | ||||||
chr2:171393337
|
G | A | 90 | a0001c0001t0001g0111a0001c0001t0001g0256a0001c0001t0001g0264others(87): Show | 91 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.-12-1140C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171393337 | ||||||
chr2:171393407
|
C | CA | 249 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(246): Show | 250 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.-12-1211dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171393407 | ||||||
chr2:171393407
|
C | CAA | 52 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(49): Show | 53 | HG00280.hp1 HG00621.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.-12-1212_-12-1211d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171393407 | ||||||
chr2:171393407
|
C | CAAA | 14 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0005g0106others(11): Show | 14 | HG00642.hp1 HG01884.hp1 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12-1213_-12-1211d others(5): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171393407 | ||||||
chr2:171393587
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-1390G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171393587 | ||||||
chr2:171393659
|
A | T | 1 | a0001c0001t0004g0263 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-12-1462T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171393659 | ||||||
chr2:171393732
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-12-1535T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171393732 | ||||||
chr2:171393853
|
C | G | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12-1656G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171393853 | ||||||
chr2:171394295
|
G | A | 15 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(12): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12-2098C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171394295 | ||||||
chr2:171394534
|
T | C | 92 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0086others(89): Show | 92 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.-12-2337A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171394534 | ||||||
chr2:171394667
|
T | C | 19 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(16): Show | 19 | HG01074.hp1 HG01261.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-12-2470A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171394667 | ||||||
chr2:171395048
|
G | A | 1 | a0001c0002t0001g0222 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-12-2851C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171395048 | ||||||
chr2:171395358
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-12-3161G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171395358 | ||||||
chr2:171395490
|
A | C | 1 | a0001c0002t0001g0224 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-12-3293T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171395490 | ||||||
chr2:171395707
|
C | T | 112 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(109): Show | 112 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.-12-3510G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171395707 | ||||||
chr2:171395875
|
C | T | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-3678G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171395875 | ||||||
chr2:171396213
|
G | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-4016C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171396213 | ||||||
chr2:171396265
|
G | GAATA | 7 | a0001c0001t0001g0068a0001c0001t0014g0209a0001c0002t0009g0290others(4): Show | 7 | HG00408.hp1 HG02040.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-4072_-12-4069d others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171396265 | ||||||
chr2:171396265
|
G | GAATAAAT others(1): Show |
17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-4076_-12-4069d others(10): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171396265 | ||||||
chr2:171396489
|
G | C | 19 | a0001c0001t0001g0038a0001c0001t0001g0094a0001c0001t0001g0126others(16): Show | 19 | HG00423.hp1 HG00438.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-12-4292C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171396489 | ||||||
chr2:171396550
|
C | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-4353G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171396550 | ||||||
chr2:171396586
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-12-4389A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171396586 | ||||||
chr2:171396724
|
A | G | 4 | a0001c0001t0012g0049a0001c0001t0012g0050a0001c0001t0012g0051others(1): Show | 4 | HG02145.hp1 HG02622.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-4527T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171396724 | ||||||
chr2:171396851
|
CT | C | 9 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-4655delA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171396851 | ||||||
chr2:171396990
|
C | CT | 21 | a0001c0001t0074g0090a0001c0002t0022g0317a0001c0002t0022g0318others(18): Show | 21 | HG01074.hp1 HG01261.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-4794dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171396990 | ||||||
chr2:171397020
|
C | T | 1 | a0001c0001t0003g0108 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-12-4823G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397020 | ||||||
chr2:171397050
|
A | G | 328 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(325): Show | 330 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.-12-4853T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397050 | ||||||
chr2:171397123
|
C | T | 18 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(15): Show | 18 | HG01069.hp1 HG01433.hp1 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12-4926G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397123 | ||||||
chr2:171397185
|
A | G | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-12-4988T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397185 | ||||||
chr2:171397187
|
G | A | 1 | a0001c0001t0071g0088 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-12-4990C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397187 | ||||||
chr2:171397206
|
A | C | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-5009T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397206 | ||||||
chr2:171397206
|
A | G | 21 | a0001c0001t0002g0011a0001c0001t0002g0048a0001c0001t0002g0087others(18): Show | 21 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-5009T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397206 | ||||||
chr2:171397352
|
T | TA | 85 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0058others(82): Show | 86 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.-12-5156dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397352 | ||||||
chr2:171397352
|
T | TAA | 81 | a0001c0001t0001g0038a0001c0001t0001g0057a0001c0001t0001g0070others(78): Show | 81 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.-12-5157_-12-5156d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397352 | ||||||
chr2:171397352
|
T | TAAA | 58 | a0001c0001t0001g0055a0001c0001t0001g0086a0001c0001t0001g0098others(55): Show | 58 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-12-5158_-12-5156d others(5): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397352 | ||||||
chr2:171397352
|
T | TAAAA | 18 | a0001c0001t0001g0039a0001c0001t0001g0094a0001c0001t0002g0011others(15): Show | 18 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12-5159_-12-5156d others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397352 | ||||||
chr2:171397352
|
TA | T | 11 | a0001c0002t0022g0318a0001c0002t0022g0320a0001c0002t0033g0324others(8): Show | 11 | HG02895.hp2 HG02896.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-5156delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397352 | ||||||
chr2:171397377
|
A | AC | 5 | a0001c0002t0001g0044a0001c0002t0001g0229a0001c0002t0008g0217others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-5181_-12-5180i others(3): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397377 | ||||||
chr2:171397377
|
A | C | 12 | a0001c0002t0001g0002a0001c0002t0001g0054a0001c0002t0001g0218others(9): Show | 13 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12-5180T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397377 | ||||||
chr2:171397512
|
C | T | 1 | a0001c0001t0003g0093 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-12-5315G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397512 | ||||||
chr2:171397521
|
T | C | 2 | a0001c0001t0004g0276a0001c0001t0030g0277 | 2 | NA18998.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-12-5324A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397521 | ||||||
chr2:171397535
|
CAG | C | 33 | a0001c0001t0001g0111a0001c0001t0003g0001a0001c0001t0003g0075others(30): Show | 34 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.-12-5340_-12-5339d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397535 | ||||||
chr2:171397543
|
A | T | 62 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(59): Show | 63 | HG00408.hp1 HG00423.hp2 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.-12-5346T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397543 | ||||||
chr2:171397553
|
C | CA | 35 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(32): Show | 35 | HG00408.hp1 HG00609.hp1 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.-12-5357dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397553 | ||||||
chr2:171397553
|
CA | C | 52 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0041others(49): Show | 52 | HG00423.hp2 HG01069.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.-12-5357delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397553 | ||||||
chr2:171397574
|
AAGAG | A | 6 | a0001c0001t0002g0168a0001c0002t0001g0218a0001c0002t0001g0221others(3): Show | 6 | HG02451.hp2 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-5381_-12-5378d others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397574 | ||||||
chr2:171397680
|
A | T | 1 | a0001c0003t0005g0029 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-12-5483T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397680 | ||||||
chr2:171397973
|
A | G | 2 | a0001c0002t0035g0326a0001c0002t0035g0327 | 2 | HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-12-5776T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171397973 | ||||||
chr2:171398012
|
T | A | 1 | a0001c0001t0003g0110 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-12-5815A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171398012 | ||||||
chr2:171398263
|
G | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-6066C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171398263 | ||||||
chr2:171398400
|
G | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-6203C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171398400 | ||||||
chr2:171398451
|
T | C | 1 | a0002c0004t0018g0092 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12-6254A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171398451 | ||||||
chr2:171398651
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12-6454T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171398651 | ||||||
chr2:171398742
|
A | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-6545T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171398742 | ||||||
chr2:171398790
|
A | G | 2 | a0001c0001t0002g0182a0001c0001t0002g0183 | 2 | NA18986.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-12-6593T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171398790 | ||||||
chr2:171398961
|
G | C | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-6764C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171398961 | ||||||
chr2:171399172
|
C | T | 91 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0086others(88): Show | 91 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.-12-6975G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171399172 | ||||||
chr2:171399238
|
C | T | 33 | a0001c0001t0001g0111a0001c0001t0003g0001a0001c0001t0003g0075others(30): Show | 34 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.-12-7041G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171399238 | ||||||
chr2:171399273
|
G | A | 328 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(325): Show | 330 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.-12-7076C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171399273 | ||||||
chr2:171399383
|
T | C | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-7186A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171399383 | ||||||
chr2:171399606
|
T | C | 1 | a0001c0003t0086g0028 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-12-7409A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171399606 | ||||||
chr2:171399609
|
C | G | 4 | a0001c0001t0004g0242a0001c0001t0004g0282a0001c0001t0004g0289others(1): Show | 4 | HG02602.hp1 NA18948.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-7412G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171399609 | ||||||
chr2:171399719
|
C | T | 9 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-7522G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171399719 | ||||||
chr2:171399941
|
T | A | 112 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(109): Show | 112 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.-12-7744A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171399941 | ||||||
chr2:171400029
|
T | C | 1 | a0001c0001t0023g0013 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-12-7832A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171400029 | ||||||
chr2:171400048
|
T | A | 7 | a0001c0001t0001g0041a0001c0001t0004g0280a0001c0001t0004g0281others(4): Show | 7 | HG01109.hp2 HG01175.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-7851A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171400048 | ||||||
chr2:171400049
|
A | T | 21 | a0001c0002t0009g0249a0001c0002t0009g0290a0001c0002t0009g0291others(18): Show | 21 | HG00408.hp1 HG01261.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12-7852T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171400049 | ||||||
chr2:171400452
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-8255G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171400452 | ||||||
chr2:171400608
|
T | C | 6 | a0001c0001t0074g0090a0002c0004t0018g0072a0002c0004t0018g0073others(3): Show | 6 | HG01074.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-8411A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171400608 | ||||||
chr2:171400845
|
G | T | 1 | a0001c0001t0004g0280 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-12-8648C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171400845 | ||||||
chr2:171401054
|
G | A | 36 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(33): Show | 36 | HG00408.hp1 HG00423.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.-12-8857C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171401054 | ||||||
chr2:171401197
|
G | A | 15 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(12): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12-9000C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171401197 | ||||||
chr2:171401767
|
A | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-9570T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171401767 | ||||||
chr2:171401841
|
T | TG | 328 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(325): Show | 330 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.-12-9645dupC | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171401841 | ||||||
chr2:171402190
|
G | A | 1 | a0001c0001t0011g0255 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-12-9993C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171402190 | ||||||
chr2:171402290
|
T | C | 1 | a0001c0001t0002g0201 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-12-10093A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171402290 | ||||||
chr2:171402329
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-12-10132T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171402329 | ||||||
chr2:171402476
|
G | A | 1 | a0001c0003t0005g0029 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-12-10279C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171402476 | ||||||
chr2:171402588
|
T | A | 3 | a0004c0008t0001g0299a0004c0008t0001g0300a0004c0008t0001g0301 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-12-10391A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171402588 | ||||||
chr2:171402688
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-12-10491G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171402688 | ||||||
chr2:171402785
|
C | G | 62 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(59): Show | 63 | HG00408.hp1 HG00423.hp2 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.-12-10588G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171402785 | ||||||
chr2:171402842
|
C | T | 1 | a0001c0002t0001g0225 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-12-10645G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171402842 | ||||||
chr2:171402990
|
A | G | 7 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(4): Show | 7 | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-10793T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171402990 | ||||||
chr2:171403054
|
C | T | 9 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-10857G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171403054 | ||||||
chr2:171403133
|
G | C | 1 | a0001c0002t0029g0056 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-12-10936C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171403133 | ||||||
chr2:171403177
|
G | A | 56 | a0001c0001t0001g0256a0001c0001t0001g0264a0001c0001t0001g0288others(53): Show | 56 | HG00597.hp1 HG01109.hp2 HG01175.hp2 others(53): Show |
intron_variant | MODIFIER | c.-12-10980C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171403177 | ||||||
chr2:171403242
|
A | C | 18 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(15): Show | 18 | HG01261.hp1 HG02280.hp2 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12-11045T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171403242 | ||||||
chr2:171403334
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-11137G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171403334 | ||||||
chr2:171403463
|
C | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0155 | 2 | HG01952.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-12-11266G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171403463 | ||||||
chr2:171403463
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-11266G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171403463 | ||||||
chr2:171403517
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-12-11320C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171403517 | ||||||
chr2:171403667
|
G | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-11470C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171403667 | ||||||
chr2:171404035
|
T | C | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-11838A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404035 | ||||||
chr2:171404052
|
C | CAT | 32 | a0001c0001t0001g0060a0001c0001t0001g0095a0001c0001t0001g0096others(29): Show | 32 | HG01081.hp1 HG01109.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.-12-11857_-12-1185 others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
C | CATAT | 39 | a0001c0001t0001g0037a0001c0001t0001g0065a0001c0001t0001g0070others(36): Show | 39 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.-12-11859_-12-1185 others(8): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
C | CATATAT | 43 | a0001c0001t0001g0038a0001c0001t0001g0055a0001c0001t0001g0058others(40): Show | 44 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.-12-11861_-12-1185 others(10): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
C | CATATATA others(1): Show |
46 | a0001c0001t0001g0057a0001c0001t0001g0066a0001c0001t0001g0111others(43): Show | 47 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.-12-11863_-12-1185 others(12): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
C | CATATATA others(3): Show |
7 | a0001c0001t0010g0257a0001c0001t0010g0286a0001c0001t0084g0247others(4): Show | 7 | HG01433.hp2 HG02970.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-11865_-12-1185 others(14): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
C | CATATATA others(5): Show |
5 | a0001c0001t0001g0288a0001c0001t0003g0081a0001c0001t0012g0050others(2): Show | 5 | HG01993.hp2 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12-11867_-12-1185 others(16): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
C | CATATATA others(7): Show |
1 | a0001c0002t0001g0227 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-12-11869_-12-1185 others(18): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
C | CATATATA others(11): Show |
1 | a0001c0002t0007g0310 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-12-11873_-12-1185 others(22): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
C | CATATATA others(17): Show |
1 | a0001c0001t0003g0110 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-12-11879_-12-1185 others(28): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
C | CATATATA others(25): Show |
1 | a0001c0001t0003g0080 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-12-11887_-12-1185 others(36): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
CAT | C | 4 | a0001c0001t0001g0043a0001c0001t0017g0204a0001c0002t0007g0309others(1): Show | 4 | HG02602.hp2 HG03195.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-11857_-12-1185 others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
CATAT | C | 6 | a0001c0001t0001g0041a0001c0001t0004g0276a0001c0001t0038g0006others(3): Show | 6 | HG02559.hp1 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-11859_-12-1185 others(8): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
CATATAT | C | 3 | a0001c0001t0003g0117a0001c0001t0030g0277a0001c0002t0001g0044 | 3 | HG02615.hp1 NA19000.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-12-11861_-12-1185 others(10): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
CATATATA others(1): Show |
C | 4 | a0001c0001t0004g0278a0001c0001t0004g0279a0001c0001t0013g0007others(1): Show | 4 | HG02615.hp2 HG03041.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-11863_-12-1185 others(12): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
CATATATA others(3): Show |
C | 12 | a0001c0001t0001g0170a0001c0001t0002g0173a0001c0001t0002g0174others(9): Show | 12 | HG00642.hp1 HG02717.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.-12-11865_-12-1185 others(14): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
CATATATA others(5): Show |
C | 15 | a0001c0001t0001g0039a0001c0001t0001g0132a0001c0001t0001g0133others(12): Show | 15 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12-11867_-12-1185 others(16): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
CATATATA others(7): Show |
C | 50 | a0001c0001t0001g0086a0001c0001t0001g0128a0001c0001t0001g0135others(47): Show | 50 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-12-11869_-12-1185 others(18): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
CATATATA others(9): Show |
C | 25 | a0001c0001t0001g0085a0001c0001t0001g0142a0001c0001t0001g0143others(22): Show | 25 | HG01074.hp2 HG01099.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.-12-11871_-12-1185 others(20): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
CATATATA others(13): Show |
C | 4 | a0001c0001t0016g0061a0001c0001t0016g0062a0001c0001t0016g0064others(1): Show | 4 | NA18952.hp2 NA18953.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-11875_-12-1185 others(24): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
CATATATA others(17): Show |
C | 2 | a0001c0003t0055g0015a0001c0003t0088g0014 | 2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-12-11879_-12-1185 others(28): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
CATATATA others(19): Show |
C | 7 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(4): Show | 7 | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-11881_-12-1185 others(30): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
CATATATA others(23): Show |
C | 1 | a0001c0001t0001g0042 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-12-11885_-12-1185 others(34): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404052
|
CATATATA others(27): Show |
C | 1 | a0002c0004t0018g0073 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-12-11889_-12-1185 others(38): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404052 | ||||||
chr2:171404295
|
T | G | 1 | a0001c0001t0002g0195 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-12-12098A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404295 | ||||||
chr2:171404349
|
C | T | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12-12152G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404349 | ||||||
chr2:171404514
|
C | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-12317G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404514 | ||||||
chr2:171404562
|
T | C | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-12365A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404562 | ||||||
chr2:171404595
|
G | A | 2 | a0001c0001t0074g0090a0002c0014t0046g0089 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-12-12398C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404595 | ||||||
chr2:171404770
|
C | A | 18 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(15): Show | 18 | HG01261.hp1 HG02280.hp2 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12-12573G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171404770 | ||||||
chr2:171405367
|
G | A | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12-13170C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171405367 | ||||||
chr2:171405558
|
G | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-13361C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171405558 | ||||||
chr2:171405658
|
GA | G | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-13462delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171405658 | ||||||
chr2:171406151
|
C | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-13954G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171406151 | ||||||
chr2:171406343
|
A | G | 1 | a0001c0001t0002g0012 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-12-14146T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171406343 | ||||||
chr2:171406372
|
T | A | 1 | a0001c0001t0001g0213 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-12-14175A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171406372 | ||||||
chr2:171406540
|
G | A | 1 | a0001c0001t0003g0121 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-12-14343C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171406540 | ||||||
chr2:171406585
|
C | T | 1 | a0001c0003t0058g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-12-14388G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171406585 | ||||||
chr2:171406590
|
G | T | 1 | a0001c0001t0078g0294 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12-14393C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171406590 | ||||||
chr2:171406938
|
T | A | 47 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(44): Show | 48 | HG00408.hp1 HG00423.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.-12-14741A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171406938 | ||||||
chr2:171407199
|
T | A | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-15002A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171407199 | ||||||
chr2:171407338
|
C | T | 1 | a0001c0001t0002g0172 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-12-15141G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171407338 | ||||||
chr2:171407486
|
G | A | 1 | a0001c0001t0002g0201 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-12-15289C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171407486 | ||||||
chr2:171407983
|
A | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-15786T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171407983 | ||||||
chr2:171407994
|
C | T | 1 | a0001c0001t0043g0171 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-12-15797G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171407994 | ||||||
chr2:171408053
|
C | T | 328 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(325): Show | 330 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.-12-15856G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171408053 | ||||||
chr2:171408287
|
AGTTTTTT others(1): Show |
A | 15 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(12): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12-16098_-12-1609 others(12): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171408287 | ||||||
chr2:171408296
|
G | GT | 8 | a0001c0001t0001g0058a0001c0001t0001g0256a0001c0001t0001g0283others(5): Show | 8 | HG01934.hp2 HG02027.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-16100dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171408296 | ||||||
chr2:171408296
|
G | T | 2 | a0001c0002t0009g0290a0001c0002t0009g0291 | 2 | HG00408.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.-12-16099C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171408296 | ||||||
chr2:171408296
|
GT | G | 40 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(37): Show | 41 | HG00423.hp2 HG01069.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.-12-16100delA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171408296 | ||||||
chr2:171408299
|
T | TG | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-16103_-12-1610 others(5): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171408299 | ||||||
chr2:171408451
|
C | T | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-16254G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171408451 | ||||||
chr2:171408504
|
T | C | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-16307A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171408504 | ||||||
chr2:171408512
|
A | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-16315T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171408512 | ||||||
chr2:171408527
|
C | A | 1 | a0001c0001t0001g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-12-16330G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171408527 | ||||||
chr2:171408745
|
T | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-16548A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171408745 | ||||||
chr2:171408871
|
C | T | 1 | a0001c0001t0011g0255 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-12-16674G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171408871 | ||||||
chr2:171408898
|
G | GT | 26 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(23): Show | 27 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-12-16702dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171408898 | ||||||
chr2:171408991
|
A | T | 2 | a0004c0008t0001g0299a0004c0008t0001g0300 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-12-16794T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171408991 | ||||||
chr2:171409006
|
T | C | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-16809A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171409006 | ||||||
chr2:171409010
|
G | T | 2 | a0004c0008t0001g0299a0004c0008t0001g0300 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-12-16813C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171409010 | ||||||
chr2:171409163
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-12-16966T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171409163 | ||||||
chr2:171409237
|
G | A | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12-17040C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171409237 | ||||||
chr2:171409363
|
C | G | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-17166G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171409363 | ||||||
chr2:171409378
|
G | GA | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-17182dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171409378 | ||||||
chr2:171409571
|
C | T | 1 | a0001c0002t0087g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-12-17374G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171409571 | ||||||
chr2:171409821
|
T | C | 1 | a0001c0001t0003g0093 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-12-17624A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171409821 | ||||||
chr2:171409904
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-12-17707G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171409904 | ||||||
chr2:171409987
|
A | G | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-17790T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171409987 | ||||||
chr2:171410097
|
C | A | 1 | a0001c0001t0001g0315 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-12-17900G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171410097 | ||||||
chr2:171410100
|
A | T | 1 | a0001c0001t0001g0315 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-12-17903T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171410100 | ||||||
chr2:171410211
|
T | C | 1 | a0001c0003t0025g0031 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-12-18014A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171410211 | ||||||
chr2:171410390
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-12-18193C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171410390 | ||||||
chr2:171410900
|
T | C | 1 | a0001c0001t0002g0168 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-12-18703A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171410900 | ||||||
chr2:171411160
|
A | G | 1 | a0001c0001t0030g0254 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-12-18963T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171411160 | ||||||
chr2:171411225
|
A | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-12-19028T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171411225 | ||||||
chr2:171411511
|
G | A | 1 | a0001c0001t0008g0169 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-12-19314C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171411511 | ||||||
chr2:171411551
|
T | C | 235 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(232): Show | 236 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(233): Show |
intron_variant | MODIFIER | c.-12-19354A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171411551 | ||||||
chr2:171411721
|
G | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-19524C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171411721 | ||||||
chr2:171412070
|
C | T | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12-19873G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171412070 | ||||||
chr2:171412225
|
C | T | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-20028G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171412225 | ||||||
chr2:171412329
|
G | A | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12-20132C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171412329 | ||||||
chr2:171412543
|
A | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-20346T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171412543 | ||||||
chr2:171412581
|
TA | T | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12-20385delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171412581 | ||||||
chr2:171412597
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-12-20400A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171412597 | ||||||
chr2:171412647
|
A | G | 121 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(118): Show | 121 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.-12-20450T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171412647 | ||||||
chr2:171412901
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-12-20704T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171412901 | ||||||
chr2:171413091
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-13+20792G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171413091 | ||||||
chr2:171413340
|
A | G | 1 | a0004c0008t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-13+20543T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171413340 | ||||||
chr2:171413435
|
G | A | 6 | a0001c0001t0001g0057a0001c0001t0001g0066a0001c0001t0001g0067others(3): Show | 6 | HG02083.hp1 NA18964.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+20448C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171413435 | ||||||
chr2:171413501
|
T | C | 19 | a0001c0001t0004g0246a0001c0001t0004g0250a0001c0001t0004g0251others(16): Show | 19 | HG00597.hp1 HG06807.hp2 NA18941.hp1 others(16): Show |
intron_variant | MODIFIER | c.-13+20382A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171413501 | ||||||
chr2:171413628
|
G | A | 1 | a0001c0001t0003g0122 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-13+20255C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171413628 | ||||||
chr2:171413763
|
T | C | 1 | a0007c0013t0082g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-13+20120A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171413763 | ||||||
chr2:171413958
|
C | T | 1 | a0001c0001t0040g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-13+19925G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171413958 | ||||||
chr2:171413982
|
A | T | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+19901T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171413982 | ||||||
chr2:171414178
|
G | A | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+19705C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171414178 | ||||||
chr2:171414179
|
A | G | 4 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292others(1): Show | 4 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+19704T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171414179 | ||||||
chr2:171414189
|
G | A | 9 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+19694C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171414189 | ||||||
chr2:171414331
|
T | C | 323 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(320): Show | 325 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(322): Show |
intron_variant | MODIFIER | c.-13+19552A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171414331 | ||||||
chr2:171414372
|
G | A | 27 | a0001c0001t0001g0038a0001c0001t0001g0094a0001c0001t0001g0126others(24): Show | 27 | HG00423.hp1 HG00438.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-13+19511C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171414372 | ||||||
chr2:171414417
|
C | CA | 27 | a0001c0001t0001g0157a0001c0001t0002g0296a0001c0001t0004g0251others(24): Show | 27 | HG00423.hp2 HG01081.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.-13+19465dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171414417 | ||||||
chr2:171414417
|
CA | C | 16 | a0001c0002t0001g0002a0001c0002t0001g0054a0001c0002t0001g0218others(13): Show | 17 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-13+19465delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171414417 | ||||||
chr2:171414592
|
G | A | 5 | a0001c0001t0012g0049a0001c0001t0012g0050a0001c0001t0012g0051others(2): Show | 5 | HG02145.hp1 HG02622.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+19291C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171414592 | ||||||
chr2:171414704
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-13+19179C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171414704 | ||||||
chr2:171414729
|
G | GA | 13 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(10): Show | 13 | HG00408.hp1 HG00558.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-13+19153dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171414729 | ||||||
chr2:171414791
|
G | C | 2 | a0001c0001t0074g0090a0002c0014t0046g0089 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-13+19092C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171414791 | ||||||
chr2:171414845
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-13+19038C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171414845 | ||||||
chr2:171414937
|
T | G | 4 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(1): Show | 4 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+18946A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171414937 | ||||||
chr2:171414969
|
A | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0170 | 2 | NA18944.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-13+18914T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171414969 | ||||||
chr2:171414992
|
C | T | 4 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(1): Show | 4 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+18891G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171414992 | ||||||
chr2:171415110
|
A | C | 2 | a0001c0001t0003g0295a0001c0001t0078g0294 | 2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-13+18773T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171415110 | ||||||
chr2:171415194
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-13+18689C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171415194 | ||||||
chr2:171415283
|
G | A | 1 | a0001c0001t0004g0281 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-13+18600C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171415283 | ||||||
chr2:171415284
|
C | A | 1 | a0001c0001t0004g0281 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-13+18599G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171415284 | ||||||
chr2:171415349
|
C | CT | 58 | a0001c0001t0001g0037a0001c0001t0001g0094a0001c0001t0001g0126others(55): Show | 58 | HG00621.hp1 HG00621.hp2 HG01074.hp1 others(55): Show |
intron_variant | MODIFIER | c.-13+18533dupA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171415349 | ||||||
chr2:171415349
|
C | CTT | 23 | a0001c0001t0003g0108a0001c0001t0004g0246a0001c0001t0010g0245others(20): Show | 23 | HG00408.hp1 HG00558.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.-13+18532_-13+1853 others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171415349 | ||||||
chr2:171415349
|
C | CTTTTT | 12 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(9): Show | 12 | HG01081.hp1 HG01884.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.-13+18529_-13+1853 others(9): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171415349 | ||||||
chr2:171415349
|
CT | C | 8 | a0001c0001t0001g0038a0001c0001t0012g0123a0001c0001t0013g0010others(5): Show | 8 | HG02258.hp1 HG02559.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+18533delA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171415349 | ||||||
chr2:171415412
|
G | A | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+18471C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171415412 | ||||||
chr2:171415413
|
C | A | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+18470G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171415413 | ||||||
chr2:171415597
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+18286C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171415597 | ||||||
chr2:171415678
|
A | G | 1 | a0001c0001t0012g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-13+18205T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171415678 | ||||||
chr2:171415772
|
G | A | 11 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(8): Show | 11 | HG02647.hp2 HG02895.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+18111C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171415772 | ||||||
chr2:171415934
|
G | A | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-13+17949C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171415934 | ||||||
chr2:171416091
|
A | G | 2 | a0001c0002t0001g0227a0001c0002t0008g0228 | 2 | HG01891.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-13+17792T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171416091 | ||||||
chr2:171416118
|
A | G | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+17765T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171416118 | ||||||
chr2:171416146
|
G | A | 5 | a0001c0001t0052g0071a0002c0004t0018g0072a0002c0004t0018g0073others(2): Show | 5 | HG01074.hp1 HG01891.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+17737C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171416146 | ||||||
chr2:171416180
|
A | C | 48 | a0001c0001t0045g0241a0001c0002t0001g0002a0001c0002t0001g0044others(45): Show | 49 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-13+17703T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171416180 | ||||||
chr2:171416593
|
C | A | 46 | a0001c0001t0045g0241a0001c0002t0001g0002a0001c0002t0001g0044others(43): Show | 47 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.-13+17290G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171416593 | ||||||
chr2:171416793
|
C | T | 22 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(19): Show | 22 | HG01069.hp1 HG01099.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-13+17090G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171416793 | ||||||
chr2:171416920
|
G | T | 1 | a0001c0001t0053g0244 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-13+16963C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171416920 | ||||||
chr2:171417270
|
A | C | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+16613T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171417270 | ||||||
chr2:171417318
|
C | T | 7 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+16565G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171417318 | ||||||
chr2:171417470
|
GCACA | G | 5 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+16409_-13+1641 others(8): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171417470 | ||||||
chr2:171417675
|
T | C | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-13+16208A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171417675 | ||||||
chr2:171417762
|
C | A | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+16121G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171417762 | ||||||
chr2:171417800
|
C | T | 3 | a0001c0002t0009g0290a0001c0002t0009g0291a0001c0002t0009g0292 | 3 | HG00408.hp1 HG02040.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.-13+16083G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171417800 | ||||||
chr2:171418044
|
C | T | 32 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(29): Show | 32 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.-13+15839G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171418044 | ||||||
chr2:171418063
|
C | A | 1 | a0001c0001t0004g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-13+15820G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171418063 | ||||||
chr2:171418139
|
G | T | 32 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(29): Show | 32 | HG00423.hp2 HG01081.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.-13+15744C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171418139 | ||||||
chr2:171418428
|
T | A | 1 | a0001c0005t0015g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-13+15455A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171418428 | ||||||
chr2:171418450
|
T | A | 4 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0107others(1): Show | 4 | HG00642.hp1 HG01256.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+15433A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171418450 | ||||||
chr2:171418507
|
C | CGGGT | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+15375_-13+1537 others(8): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171418507 | ||||||
chr2:171418509
|
A | C | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+15374T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171418509 | ||||||
chr2:171418510
|
T | A | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+15373A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171418510 | ||||||
chr2:171418513
|
G | C | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+15370C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171418513 | ||||||
chr2:171418517
|
C | CCCA | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+15365_-13+1536 others(7): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171418517 | ||||||
chr2:171418586
|
T | C | 29 | a0001c0001t0045g0241a0001c0002t0002g0302a0001c0002t0007g0298others(26): Show | 29 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.-13+15297A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171418586 | ||||||
chr2:171418975
|
C | T | 7 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+14908G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171418975 | ||||||
chr2:171419021
|
C | CA | 13 | a0001c0001t0006g0199a0001c0001t0040g0198a0001c0001t0052g0071others(10): Show | 13 | HG01074.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-13+14861dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171419021 | ||||||
chr2:171419021
|
CA | C | 25 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(22): Show | 25 | HG00408.hp1 HG00558.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.-13+14861delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171419021 | ||||||
chr2:171419058
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-13+14825A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171419058 | ||||||
chr2:171419059
|
A | G | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-13+14824T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171419059 | ||||||
chr2:171419060
|
T | A | 15 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(12): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.-13+14823A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171419060 | ||||||
chr2:171419345
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-13+14538A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171419345 | ||||||
chr2:171419379
|
C | A | 3 | a0001c0001t0002g0201a0001c0001t0006g0035a0001c0001t0006g0200 | 3 | NA19064.hp1 NA19068.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-13+14504G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171419379 | ||||||
chr2:171419516
|
G | C | 1 | a0001c0001t0001g0159 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-13+14367C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171419516 | ||||||
chr2:171419522
|
T | G | 1 | a0001c0001t0003g0295 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-13+14361A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171419522 | ||||||
chr2:171419618
|
T | G | 1 | a0001c0002t0001g0002 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-13+14265A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171419618 | ||||||
chr2:171419635
|
C | G | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+14248G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171419635 | ||||||
chr2:171419647
|
T | C | 1 | a0001c0001t0012g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-13+14236A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171419647 | ||||||
chr2:171419681
|
A | C | 5 | a0001c0002t0001g0218a0001c0002t0001g0221a0001c0002t0001g0222others(2): Show | 5 | HG02451.hp2 HG02486.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+14202T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171419681 | ||||||
chr2:171419768
|
C | T | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-13+14115G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171419768 | ||||||
chr2:171419841
|
A | G | 2 | a0004c0008t0001g0299a0004c0008t0001g0300 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-13+14042T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171419841 | ||||||
chr2:171420026
|
C | T | 1 | a0001c0001t0010g0285 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-13+13857G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171420026 | ||||||
chr2:171420232
|
G | A | 7 | a0001c0001t0052g0071a0001c0001t0074g0090a0002c0004t0018g0072others(4): Show | 7 | HG01074.hp1 HG01891.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+13651C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171420232 | ||||||
chr2:171420310
|
C | T | 2 | a0001c0003t0055g0015a0001c0003t0088g0014 | 2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-13+13573G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171420310 | ||||||
chr2:171420311
|
G | A | 1 | a0001c0001t0004g0084 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-13+13572C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171420311 | ||||||
chr2:171420518
|
A | G | 7 | a0001c0001t0052g0071a0001c0001t0074g0090a0002c0004t0018g0072others(4): Show | 7 | HG01074.hp1 HG01891.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+13365T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171420518 | ||||||
chr2:171420528
|
C | A | 4 | a0001c0003t0021g0237a0001c0003t0021g0239a0001c0003t0021g0240others(1): Show | 4 | HG02258.hp1 HG02559.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+13355G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171420528 | ||||||
chr2:171420754
|
T | C | 90 | a0001c0001t0001g0111a0001c0001t0001g0256a0001c0001t0001g0264others(87): Show | 91 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.-13+13129A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171420754 | ||||||
chr2:171420895
|
C | A | 7 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+12988G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171420895 | ||||||
chr2:171421096
|
C | A | 1 | a0001c0002t0054g0016 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-13+12787G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421096 | ||||||
chr2:171421117
|
C | G | 95 | a0001c0001t0001g0256a0001c0001t0001g0264a0001c0001t0001g0283others(92): Show | 95 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.-13+12766G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421117 | ||||||
chr2:171421181
|
T | G | 1 | a0001c0001t0004g0282 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-13+12702A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421181 | ||||||
chr2:171421270
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-13+12613G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421270 | ||||||
chr2:171421384
|
C | T | 7 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+12499G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421384 | ||||||
chr2:171421416
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-13+12467G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421416 | ||||||
chr2:171421443
|
T | C | 29 | a0001c0001t0045g0241a0001c0002t0002g0302a0001c0002t0007g0298others(26): Show | 29 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.-13+12440A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421443 | ||||||
chr2:171421449
|
CA | C | 323 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(320): Show | 325 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(322): Show |
intron_variant | MODIFIER | c.-13+12433delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421449 | ||||||
chr2:171421468
|
C | T | 2 | a0001c0001t0003g0093a0001c0001t0003g0125 | 2 | NA18984.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-13+12415G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421468 | ||||||
chr2:171421476
|
TAC | T | 300 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(297): Show | 302 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(299): Show |
intron_variant | MODIFIER | c.-13+12405_-13+1240 others(6): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421476 | ||||||
chr2:171421476
|
TACAC | T | 7 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+12403_-13+1240 others(8): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421476 | ||||||
chr2:171421539
|
T | C | 7 | a0001c0001t0052g0071a0001c0001t0074g0090a0002c0004t0018g0072others(4): Show | 7 | HG01074.hp1 HG01891.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+12344A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421539 | ||||||
chr2:171421550
|
G | C | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-13+12333C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421550 | ||||||
chr2:171421608
|
T | G | 1 | a0001c0001t0001g0213 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-13+12275A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421608 | ||||||
chr2:171421740
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-13+12143A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421740 | ||||||
chr2:171421748
|
G | A | 7 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+12135C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171421748 | ||||||
chr2:171422001
|
T | C | 1 | a0001c0001t0001g0283 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-13+11882A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171422001 | ||||||
chr2:171422173
|
A | G | 7 | a0001c0001t0052g0071a0001c0001t0074g0090a0002c0004t0018g0072others(4): Show | 7 | HG01074.hp1 HG01891.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+11710T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171422173 | ||||||
chr2:171422184
|
C | T | 35 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0132others(32): Show | 35 | HG00438.hp2 HG00609.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-13+11699G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171422184 | ||||||
chr2:171422253
|
T | G | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+11630A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171422253 | ||||||
chr2:171422516
|
A | G | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+11367T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171422516 | ||||||
chr2:171422583
|
C | CGGAGAAA others(4): Show |
1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-13+11289_-13+1129 others(15): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171422583 | ||||||
chr2:171422592
|
A | G | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-13+11291T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171422592 | ||||||
chr2:171422921
|
T | C | 1 | a0001c0001t0014g0216 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-13+10962A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171422921 | ||||||
chr2:171422984
|
T | C | 14 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(11): Show | 14 | HG00408.hp1 HG00558.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+10899A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171422984 | ||||||
chr2:171424119
|
G | C | 1 | a0001c0001t0080g0284 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-13+9764C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424119 | ||||||
chr2:171424184
|
A | G | 1 | a0001c0002t0029g0056 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-13+9699T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424184 | ||||||
chr2:171424237
|
T | A | 1 | a0001c0001t0003g0125 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-13+9646A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424237 | ||||||
chr2:171424251
|
T | C | 1 | a0001c0002t0001g0002 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-13+9632A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424251 | ||||||
chr2:171424336
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-13+9547C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424336 | ||||||
chr2:171424486
|
G | A | 7 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+9397C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424486 | ||||||
chr2:171424487
|
C | A | 48 | a0001c0001t0001g0256a0001c0001t0001g0264a0001c0001t0001g0283others(45): Show | 48 | HG00597.hp1 HG01109.hp2 HG01175.hp2 others(45): Show |
intron_variant | MODIFIER | c.-13+9396G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424487 | ||||||
chr2:171424861
|
C | T | 109 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(106): Show | 109 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.-13+9022G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424861 | ||||||
chr2:171424924
|
C | T | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-13+8959G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424924 | ||||||
chr2:171424940
|
T | C | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-13+8943A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424940 | ||||||
chr2:171424942
|
G | T | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-13+8941C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424942 | ||||||
chr2:171424944
|
G | C | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-13+8939C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424944 | ||||||
chr2:171424945
|
G | C | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-13+8938C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424945 | ||||||
chr2:171424946
|
G | A | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-13+8937C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424946 | ||||||
chr2:171424948
|
G | A | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-13+8935C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424948 | ||||||
chr2:171424949
|
G | C | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-13+8934C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424949 | ||||||
chr2:171424950
|
G | C | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-13+8933C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424950 | ||||||
chr2:171424964
|
T | C | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-13+8919A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424964 | ||||||
chr2:171424967
|
C | A | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-13+8916G>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424967 | ||||||
chr2:171424969
|
G | C | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-13+8914C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424969 | ||||||
chr2:171424973
|
CATGGGGG others(5): Show |
C | 1 | a0001c0002t0009g0293 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-13+8898_-13+8909d others(14): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171424973 | ||||||
chr2:171425048
|
G | A | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+8835C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171425048 | ||||||
chr2:171425207
|
C | T | 4 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+8676G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171425207 | ||||||
chr2:171425239
|
G | C | 2 | a0001c0001t0001g0086a0001c0001t0011g0202 | 2 | HG01934.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-13+8644C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171425239 | ||||||
chr2:171425286
|
G | A | 1 | a0001c0001t0036g0003 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-13+8597C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171425286 | ||||||
chr2:171425578
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-13+8305T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171425578 | ||||||
chr2:171425581
|
G | A | 1 | a0001c0002t0061g0314 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-13+8302C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171425581 | ||||||
chr2:171425797
|
C | T | 1 | a0001c0003t0005g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-13+8086G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171425797 | ||||||
chr2:171425827
|
G | T | 15 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(12): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.-13+8056C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171425827 | ||||||
chr2:171425951
|
G | A | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+7932C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171425951 | ||||||
chr2:171425953
|
T | C | 19 | a0001c0001t0001g0038a0001c0001t0001g0126a0001c0001t0001g0203others(16): Show | 19 | HG00423.hp1 HG00438.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-13+7930A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171425953 | ||||||
chr2:171426014
|
G | A | 1 | a0001c0001t0003g0127 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-13+7869C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171426014 | ||||||
chr2:171426104
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-13+7779G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171426104 | ||||||
chr2:171426277
|
G | A | 7 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+7606C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171426277 | ||||||
chr2:171426312
|
A | G | 1 | a0001c0001t0036g0003 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-13+7571T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171426312 | ||||||
chr2:171426590
|
A | G | 1 | a0001c0003t0019g0024 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-13+7293T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171426590 | ||||||
chr2:171426605
|
C | T | 1 | a0001c0001t0067g0243 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-13+7278G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171426605 | ||||||
chr2:171427003
|
G | A | 108 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(105): Show | 108 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-13+6880C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171427003 | ||||||
chr2:171427094
|
T | C | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-13+6789A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171427094 | ||||||
chr2:171427109
|
C | T | 1 | a0001c0002t0001g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-13+6774G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171427109 | ||||||
chr2:171427202
|
A | C | 1 | a0001c0001t0071g0088 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-13+6681T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171427202 | ||||||
chr2:171427207
|
C | T | 29 | a0001c0001t0045g0241a0001c0002t0002g0302a0001c0002t0007g0298others(26): Show | 29 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.-13+6676G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171427207 | ||||||
chr2:171427248
|
C | T | 2 | a0002c0004t0034g0328a0002c0004t0034g0329 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-13+6635G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171427248 | ||||||
chr2:171427311
|
C | T | 2 | a0004c0008t0001g0299a0004c0008t0001g0300 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-13+6572G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171427311 | ||||||
chr2:171427494
|
T | C | 14 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(11): Show | 14 | HG00408.hp1 HG00558.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+6389A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171427494 | ||||||
chr2:171427666
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-13+6217G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171427666 | ||||||
chr2:171427676
|
T | C | 2 | a0002c0004t0034g0328a0002c0004t0034g0329 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-13+6207A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171427676 | ||||||
chr2:171427722
|
C | T | 1 | a0001c0002t0033g0330 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-13+6161G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171427722 | ||||||
chr2:171427885
|
C | T | 1 | a0001c0002t0054g0016 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-13+5998G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171427885 | ||||||
chr2:171428048
|
A | C | 1 | a0001c0002t0091g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-13+5835T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171428048 | ||||||
chr2:171428145
|
T | C | 2 | a0001c0001t0002g0214a0001c0001t0002g0215 | 2 | NA19005.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-13+5738A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171428145 | ||||||
chr2:171428493
|
TA | T | 23 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0003g0001others(20): Show | 24 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.-13+5389delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171428493 | ||||||
chr2:171428525
|
T | G | 4 | a0001c0001t0001g0288a0001c0001t0010g0285a0001c0001t0010g0286others(1): Show | 4 | HG01258.hp1 HG01433.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+5358A>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171428525 | ||||||
chr2:171428542
|
T | C | 1 | a0001c0002t0001g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-13+5341A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171428542 | ||||||
chr2:171428634
|
C | G | 15 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(12): Show | 15 | HG01109.hp1 HG01975.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.-13+5249G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171428634 | ||||||
chr2:171428981
|
C | T | 1 | a0007c0013t0082g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-13+4902G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171428981 | ||||||
chr2:171429122
|
C | CA | 18 | a0001c0001t0004g0289a0001c0002t0002g0302a0001c0002t0007g0298others(15): Show | 18 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-13+4760dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171429122 | ||||||
chr2:171429122
|
CA | C | 20 | a0001c0001t0001g0055a0001c0001t0078g0294a0001c0002t0008g0217others(17): Show | 20 | HG01069.hp1 HG01169.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-13+4760delT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171429122 | ||||||
chr2:171429503
|
T | A | 1 | a0001c0001t0014g0216 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-13+4380A>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171429503 | ||||||
chr2:171429531
|
T | C | 17 | a0001c0002t0001g0002a0001c0002t0001g0044a0001c0002t0001g0054others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-13+4352A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171429531 | ||||||
chr2:171429660
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-13+4223G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171429660 | ||||||
chr2:171429823
|
T | C | 1 | a0001c0001t0028g0231 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-13+4060A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171429823 | ||||||
chr2:171429889
|
A | T | 1 | a0001c0001t0004g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-13+3994T>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171429889 | ||||||
chr2:171430024
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-13+3859C>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171430024 | ||||||
chr2:171430071
|
C | T | 1 | a0001c0002t0007g0298 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-13+3812G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171430071 | ||||||
chr2:171430186
|
C | T | 1 | a0001c0001t0017g0053 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-13+3697G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171430186 | ||||||
chr2:171430286
|
A | C | 4 | a0001c0001t0012g0049a0001c0001t0012g0050a0001c0001t0012g0051others(1): Show | 4 | HG02145.hp1 HG02622.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+3597T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171430286 | ||||||
chr2:171430294
|
G | A | 1 | a0001c0001t0003g0232 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-13+3589C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171430294 | ||||||
chr2:171430307
|
G | A | 1 | a0001c0003t0083g0032 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-13+3576C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171430307 | ||||||
chr2:171430388
|
T | C | 22 | a0001c0001t0045g0241a0001c0002t0002g0302a0001c0002t0007g0298others(19): Show | 22 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.-13+3495A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171430388 | ||||||
chr2:171430568
|
T | C | 1 | a0001c0001t0002g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-13+3315A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171430568 | ||||||
chr2:171430577
|
G | A | 1 | a0001c0001t0008g0234 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-13+3306C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171430577 | ||||||
chr2:171430940
|
A | C | 5 | a0001c0001t0045g0241a0001c0002t0009g0290a0001c0002t0009g0291others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+2943T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171430940 | ||||||
chr2:171431029
|
A | C | 37 | a0001c0001t0045g0241a0001c0002t0002g0302a0001c0002t0007g0298others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.-13+2854T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431029 | ||||||
chr2:171431030
|
A | C | 37 | a0001c0001t0045g0241a0001c0002t0002g0302a0001c0002t0007g0298others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.-13+2853T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431030 | ||||||
chr2:171431058
|
G | A | 17 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(14): Show | 17 | HG01261.hp1 HG01515.hp1 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.-13+2825C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431058 | ||||||
chr2:171431208
|
A | G | 1 | a0001c0001t0002g0048 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-13+2675T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431208 | ||||||
chr2:171431244
|
CAT | C | 15 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0022g0320others(12): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.-13+2637_-13+2638d others(4): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431244 | ||||||
chr2:171431377
|
G | A | 2 | a0005c0007t0005g0235a0007c0013t0082g0297 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-13+2506C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431377 | ||||||
chr2:171431400
|
T | C | 7 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+2483A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431400 | ||||||
chr2:171431555
|
A | C | 1 | a0001c0001t0008g0047 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-13+2328T>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431555 | ||||||
chr2:171431569
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0008g0046a0001c0001t0062g0045 | 3 | HG00423.hp1 NA18951.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.-13+2314G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431569 | ||||||
chr2:171431665
|
C | T | 48 | a0001c0001t0001g0256a0001c0001t0001g0264a0001c0001t0001g0283others(45): Show | 48 | HG00597.hp1 HG01109.hp2 HG01175.hp2 others(45): Show |
intron_variant | MODIFIER | c.-13+2218G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431665 | ||||||
chr2:171431690
|
C | T | 1 | a0001c0002t0001g0044 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-13+2193G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431690 | ||||||
chr2:171431691
|
G | T | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+2192C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431691 | ||||||
chr2:171431757
|
G | A | 1 | a0001c0001t0012g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-13+2126C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431757 | ||||||
chr2:171431827
|
A | G | 48 | a0001c0001t0001g0256a0001c0001t0001g0264a0001c0001t0001g0283others(45): Show | 48 | HG00597.hp1 HG01109.hp2 HG01175.hp2 others(45): Show |
intron_variant | MODIFIER | c.-13+2056T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431827 | ||||||
chr2:171431834
|
CT | C | 11 | a0001c0001t0068g0026a0001c0003t0005g0025a0001c0003t0005g0029others(8): Show | 11 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+2048delA | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431834 | ||||||
chr2:171431931
|
G | A | 7 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+1952C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431931 | ||||||
chr2:171431939
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-13+1944G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431939 | ||||||
chr2:171431969
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-13+1914G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431969 | ||||||
chr2:171431994
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-13+1889G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171431994 | ||||||
chr2:171432135
|
A | G | 1 | a0001c0001t0045g0241 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-13+1748T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171432135 | ||||||
chr2:171432140
|
T | C | 4 | a0001c0003t0021g0237a0001c0003t0021g0239a0001c0003t0021g0240others(1): Show | 4 | HG02258.hp1 HG02559.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+1743A>G | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171432140 | ||||||
chr2:171432192
|
C | G | 1 | a0001c0001t0002g0036 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-13+1691G>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171432192 | ||||||
chr2:171432226
|
C | CA | 66 | a0001c0001t0001g0256a0001c0001t0001g0264a0001c0001t0001g0283others(63): Show | 66 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-13+1656dupT | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171432226 | ||||||
chr2:171432637
|
C | T | 1 | a0001c0001t0006g0035 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-13+1246G>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171432637 | ||||||
chr2:171433087
|
G | A | 17 | a0001c0002t0002g0302a0001c0002t0007g0298a0001c0002t0007g0303others(14): Show | 17 | HG00423.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-13+796C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171433087 | ||||||
chr2:171433301
|
CTCA | C | 14 | a0001c0001t0068g0026a0001c0003t0005g0021a0001c0003t0005g0022others(11): Show | 14 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.-13+579_-13+581del others(3): Show |
METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171433301 | ||||||
chr2:171433473
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-13+410C>T | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171433473 | ||||||
chr2:171433664
|
G | T | 7 | a0001c0002t0054g0016a0001c0002t0072g0017a0001c0003t0019g0019others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+219C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171433664 | ||||||
chr2:171433706
|
A | G | 2 | a0001c0001t0002g0012a0001c0001t0023g0013 | 2 | HG02027.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-13+177T>C | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171433706 | ||||||
chr2:171433773
|
G | T | 1 | a0001c0001t0002g0011 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-13+110C>A | METTL8 | ENSG00000123600.21 | transcript | ENST00000375258.9 | protein_coding | 1/9 | chr2 | 171433773 |