Item | Value |
---|---|
geneid | 154743 |
ensemblid | ENSG00000164603.12 |
hgncid | 26475 |
symbol | BMT2 |
name | base methyltransferase of 25S rRNA 2 homolog |
refseq_nuc | NM_152556.3 |
refseq_prot | NP_689769.2 |
ensembl_nuc | ENST00000297145.9 |
ensembl_prot | ENSP00000297145.4 |
mane_status | MANE Select |
chr | chr7 |
start | 112819147 |
end | 112939875 |
strand | - |
ver | v1.2 |
region | chr7:112819147-112939875 |
region5000 | chr7:112814147-112944875 |
regionname0 | BMT2_chr7_112819147_112939875 |
regionname5000 | BMT2_chr7_112814147_112944875 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 405 | 206 | 90 | 46 | 34 | 8 | 26 | 22 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2723 | 84 | 23 | 21 | 21 | 4 | 13 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
t0002 | 0/0 | 2723 | 36 | 12 | 14 | 6 | 1 | 3 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
t0003 | 0/0 | 2723 | 21 | 16 | 2 | 0 | 0 | 3 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
t0004 | 0/0 | 2723 | 16 | 16 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
t0005 | 0/0 | 2723 | 15 | 1 | 4 | 0 | 3 | 7 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
t0006 | 0/0 | 2723 | 9 | 9 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
t0007 | 0/0 | 2723 | 6 | 2 | 4 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
t0008 | 0/0 | 2723 | 5 | 4 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
t0009 | 0/0 | 2723 | 5 | 5 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
t0010 | 0/0 | 2723 | 4 | 0 | 0 | 4 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
t0011 | 0/0 | 2723 | 3 | 0 | 0 | 3 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
t0012 | 0/0 | 2723 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
t0013 | 0/0 | 2723 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1218 | 200 | 85 | 45 | 34 | 8 | 26 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 | |
a0001c0002 | 0/0 | 1218 | 6 | 5 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3940 | 84 | 23 | 21 | 21 | 4 | 13 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
a0001c0001t0002 | 0/0 | 3940 | 36 | 12 | 14 | 6 | 1 | 3 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
a0001c0001t0003 | 0/0 | 3940 | 20 | 15 | 2 | 0 | 0 | 3 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
a0001c0001t0004 | 0/0 | 3940 | 16 | 16 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
a0001c0001t0005 | 0/0 | 3940 | 15 | 1 | 4 | 0 | 3 | 7 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
a0001c0001t0006 | 0/0 | 3940 | 9 | 9 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
a0001c0001t0007 | 0/0 | 3940 | 6 | 2 | 4 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
a0001c0001t0009 | 0/0 | 3940 | 5 | 5 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
a0001c0001t0010 | 0/0 | 3940 | 4 | 0 | 0 | 4 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
a0001c0001t0011 | 0/0 | 3940 | 3 | 0 | 0 | 3 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
a0001c0001t0012 | 0/0 | 3940 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
a0001c0001t0013 | 0/0 | 3940 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
a0001c0002t0003 | 0/0 | 3940 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
a0001c0002t0008 | 0/0 | 3940 | 5 | 4 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | copy fasta | chr7 | 112814147 | 112944875 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0005g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0005g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0007g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0007g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0007g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0007g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0009g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0009g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0009g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0010g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0010g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0010g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0011g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0011g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0012g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0001t0013g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0002t0008g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0002t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0002t0008g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
a0001c0002t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0199 | EUR | GBR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | GBR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG00639 | hp2 | a0001 | c0001 | t0007 | g0009 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG00673 | hp2 | a0001 | c0001 | t0010 | g0105 | EAS | CHS | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01099 | hp1 | a0001 | c0001 | t0005 | g0196 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01175 | hp1 | a0001 | c0001 | t0007 | g0012 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01192 | hp2 | a0001 | c0002 | t0008 | g0036 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01257 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01258 | hp2 | a0001 | c0001 | t0007 | g0011 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0194 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0195 | EUR | IBS | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0197 | EUR | IBS | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | IBS | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01884 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0193 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02056 | hp1 | a0001 | c0001 | t0010 | g0109 | EAS | KHV | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0064 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02148 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CDX | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0061 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0085 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02622 | hp1 | a0001 | c0002 | t0008 | g0002 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02630 | hp1 | a0001 | c0002 | t0008 | g0034 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0087 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0198 | SAS | PJL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0070 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02896 | hp2 | a0001 | c0002 | t0008 | g0037 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02922 | hp2 | a0001 | c0001 | t0013 | g0038 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | GWD | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0086 | AFR | MSL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03098 | hp2 | a0001 | c0002 | t0003 | g0035 | AFR | MSL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | MSL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0090 | AFR | MSL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0191 | SAS | PJL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | MSL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03490 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03492 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03516 | hp1 | a0001 | c0002 | t0008 | g0002 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03704 | hp2 | a0001 | c0001 | t0005 | g0192 | SAS | PJL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | BEB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0030 | SAS | BEB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0189 | SAS | BEB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | STU | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0190 | SAS | STU | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | STU | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA18522 | hp1 | a0001 | c0001 | t0009 | g0091 | AFR | YRI | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | YRI | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | YRI | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | YRI | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA18950 | hp1 | a0001 | c0001 | t0011 | g0071 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA18951 | hp1 | a0001 | c0001 | t0010 | g0104 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19009 | hp2 | a0001 | c0001 | t0010 | g0103 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | LWK | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19060 | hp1 | a0001 | c0001 | t0011 | g0073 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19066 | hp2 | a0001 | c0001 | t0011 | g0072 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | ASW | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ASW | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | TSI | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0068 | EUR | TSI | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | GIH | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | GIH | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02109 | hp1 | a0001 | c0001 | t0012 | g0028 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0059 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02486 | hp1 | a0001 | c0001 | t0006 | g0062 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02486 | hp2 | a0001 | c0001 | t0009 | g0089 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG02559 | hp2 | a0001 | c0001 | t0009 | g0088 | AFR | ACB | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0060 | AFR | MSL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | USA | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | USA | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | USA | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | USA | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0184 | REF | REF | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0092 | REF | REF | BMT2_chr7_112814147_112944875 | BMT2 | chr7 | 112814147 | 112944875 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:112822146 | T | C | 1 | a0001c0002 | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
synonymous_variant | LOW | c.816A>G | p.Leu272Leu | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 5/5 | 941/3940 | 816/1218 | 272/405 | chr7 | 112822146 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:112819580 | G | A | 2 | a0001c0001t0006a0001c0001t0007 | 15 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2164C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 5/5 | 2164 | chr7 | 112819580 | |||||
chr7:112819597 | T | A | 4 | a0001c0001t0002a0001c0001t0004a0001c0001t0010others(1): Show | 57 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2147A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 5/5 | 2147 | chr7 | 112819597 | |||||
chr7:112819715 | T | C | 1 | a0001c0001t0011 | 3 | NA18950.hp1 NA19060.hp1 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2029A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 5/5 | 2029 | chr7 | 112819715 | |||||
chr7:112819804 | G | A | 1 | a0001c0002t0008 | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1940C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 5/5 | 1940 | chr7 | 112819804 | |||||
chr7:112821553 | A | G | 1 | a0001c0001t0010 | 4 | HG00673.hp2 HG02056.hp1 NA18951.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*191T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 5/5 | 191 | chr7 | 112821553 | |||||
chr7:112821583 | A | G | 1 | a0001c0001t0009 | 5 | HG02486.hp2 HG02559.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*161T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 5/5 | 161 | chr7 | 112821583 | |||||
chr7:112939760 | G | T | 1 | a0001c0001t0004 | 16 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-10C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/5 | 10 | chr7 | 112939760 | |||||
chr7:112939808 | G | A | 1 | a0001c0001t0005 | 15 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-58C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/5 | 58 | chr7 | 112939808 | |||||
chr7:112939827 | A | G | 1 | a0001c0001t0013 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-77T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/5 | 77 | chr7 | 112939827 | |||||
chr7:112939865 | A | G | 5 | a0001c0001t0003a0001c0001t0007a0001c0001t0012others(2): Show | 33 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-115T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/5 | 115 | chr7 | 112939865 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:112822458 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-85T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112822458 | ||||||
chr7:112822580 | T | A | 17 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(14): Show | 17 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.589-207A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112822580 | ||||||
chr7:112823135 | T | C | 5 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(2): Show | 5 | HG02922.hp2 NA18947.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-762A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112823135 | ||||||
chr7:112823259 | T | A | 1 | a0001c0001t0001g0150 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.589-886A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112823259 | ||||||
chr7:112823304 | G | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-931C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112823304 | ||||||
chr7:112823527 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.589-1154G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112823527 | ||||||
chr7:112823567 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.589-1194G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112823567 | ||||||
chr7:112823642 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-1269A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112823642 | ||||||
chr7:112823706 | T | C | 1 | a0001c0001t0003g0019 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.589-1333A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112823706 | ||||||
chr7:112823936 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.589-1563G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112823936 | ||||||
chr7:112824061 | C | CTTTA | 117 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0186others(114): Show | 121 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(118): Show |
intron_variant | MODIFIER | c.589-1692_589-1689d others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112824061 | ||||||
chr7:112824468 | C | G | 7 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0082others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-2095G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112824468 | ||||||
chr7:112824491 | T | A | 5 | a0001c0001t0001g0131a0001c0001t0001g0148a0001c0001t0001g0157others(2): Show | 5 | HG00639.hp2 HG01175.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-2118A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112824491 | ||||||
chr7:112824500 | C | T | 5 | a0001c0001t0001g0131a0001c0001t0001g0148a0001c0001t0001g0157others(2): Show | 5 | HG00639.hp2 HG01175.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-2127G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112824500 | ||||||
chr7:112824501 | T | A | 5 | a0001c0001t0001g0131a0001c0001t0001g0148a0001c0001t0001g0157others(2): Show | 5 | HG00639.hp2 HG01175.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-2128A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112824501 | ||||||
chr7:112824641 | A | G | 13 | a0001c0001t0001g0177a0001c0001t0002g0069a0001c0001t0002g0079others(10): Show | 13 | HG00099.hp2 HG01168.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.589-2268T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112824641 | ||||||
chr7:112824645 | T | G | 1 | a0001c0001t0001g0177 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.589-2272A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112824645 | ||||||
chr7:112824786 | C | T | 123 | a0001c0001t0001g0056a0001c0001t0001g0074a0001c0001t0001g0075others(120): Show | 127 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(124): Show |
intron_variant | MODIFIER | c.589-2413G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112824786 | ||||||
chr7:112824787 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.589-2414C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112824787 | ||||||
chr7:112824932 | A | T | 13 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(10): Show | 15 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.589-2559T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112824932 | ||||||
chr7:112824935 | T | C | 24 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0096others(21): Show | 25 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.589-2562A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112824935 | ||||||
chr7:112825102 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.589-2729T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112825102 | ||||||
chr7:112825112 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.589-2739A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112825112 | ||||||
chr7:112825124 | C | G | 5 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(2): Show | 5 | HG01243.hp2 HG02717.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-2751G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112825124 | ||||||
chr7:112825296 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.589-2923G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112825296 | ||||||
chr7:112825349 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.589-2976T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112825349 | ||||||
chr7:112825582 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.589-3209A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112825582 | ||||||
chr7:112825596 | G | C | 1 | a0001c0001t0001g0183 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.589-3223C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112825596 | ||||||
chr7:112825756 | G | C | 18 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(15): Show | 18 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.589-3383C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112825756 | ||||||
chr7:112825792 | T | C | 2 | a0001c0001t0011g0072a0001c0001t0011g0073 | 2 | NA19060.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.589-3419A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112825792 | ||||||
chr7:112825853 | G | GT | 6 | a0001c0001t0002g0084a0001c0002t0003g0035a0001c0002t0008g0002others(3): Show | 7 | HG01168.hp1 HG01192.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-3481dupA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112825853 | ||||||
chr7:112825853 | GT | G | 5 | a0001c0001t0002g0066a0001c0001t0002g0069a0001c0001t0004g0050others(2): Show | 5 | HG02615.hp1 HG02809.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-3481delA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112825853 | ||||||
chr7:112825869 | T | A | 1 | a0001c0001t0003g0022 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.589-3496A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112825869 | ||||||
chr7:112826286 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-3913C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112826286 | ||||||
chr7:112826292 | G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG01433.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.589-3919C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112826292 | ||||||
chr7:112826298 | A | G | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG02818.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-3925T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112826298 | ||||||
chr7:112826474 | A | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-4101T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112826474 | ||||||
chr7:112826654 | T | TTTCTTGT others(2): Show |
5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-4282_589-4281i others(11): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112826654 | ||||||
chr7:112826957 | C | T | 10 | a0001c0001t0006g0059a0001c0001t0006g0061a0001c0001t0006g0086others(7): Show | 10 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.589-4584G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112826957 | ||||||
chr7:112827429 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.589-5056T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112827429 | ||||||
chr7:112827572 | G | A | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.588+4989C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112827572 | ||||||
chr7:112827748 | G | A | 1 | a0001c0002t0003g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.588+4813C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112827748 | ||||||
chr7:112827832 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+4729G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112827832 | ||||||
chr7:112827996 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+4565A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112827996 | ||||||
chr7:112828017 | G | A | 7 | a0001c0001t0002g0110a0001c0001t0002g0112a0001c0001t0002g0113others(4): Show | 7 | HG00738.hp2 HG01167.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+4544C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112828017 | ||||||
chr7:112828293 | T | A | 1 | a0001c0002t0003g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.588+4268A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112828293 | ||||||
chr7:112828529 | C | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+4032G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112828529 | ||||||
chr7:112828648 | ATTATCT | A | 10 | a0001c0001t0006g0059a0001c0001t0006g0061a0001c0001t0006g0086others(7): Show | 10 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.588+3907_588+3912d others(8): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112828648 | ||||||
chr7:112828803 | A | AATT | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+3755_588+3757d others(5): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112828803 | ||||||
chr7:112829000 | T | C | 4 | a0001c0002t0008g0002a0001c0002t0008g0034a0001c0002t0008g0036others(1): Show | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+3561A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112829000 | ||||||
chr7:112829200 | T | A | 1 | a0001c0001t0001g0173 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.588+3361A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112829200 | ||||||
chr7:112829244 | T | A | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.588+3317A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112829244 | ||||||
chr7:112829618 | A | G | 68 | a0001c0001t0001g0075a0001c0001t0001g0187a0001c0001t0002g0003others(65): Show | 69 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.588+2943T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112829618 | ||||||
chr7:112829723 | A | G | 122 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0186others(119): Show | 126 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.588+2838T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112829723 | ||||||
chr7:112829738 | T | C | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.588+2823A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112829738 | ||||||
chr7:112829749 | C | T | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+2812G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112829749 | ||||||
chr7:112830080 | C | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.588+2481G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112830080 | ||||||
chr7:112830740 | T | A | 1 | a0001c0001t0009g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.588+1821A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112830740 | ||||||
chr7:112830868 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+1693T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112830868 | ||||||
chr7:112830871 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.588+1690G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112830871 | ||||||
chr7:112830880 | CT | C | 27 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0131others(24): Show | 28 | HG00639.hp2 HG00735.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.588+1680delA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112830880 | ||||||
chr7:112831309 | C | G | 1 | a0001c0001t0002g0079 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.588+1252G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112831309 | ||||||
chr7:112831653 | A | T | 7 | a0001c0001t0005g0005a0001c0001t0005g0194a0001c0001t0005g0195others(4): Show | 8 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+908T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112831653 | ||||||
chr7:112831773 | T | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG01433.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.588+788A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112831773 | ||||||
chr7:112832012 | C | CT | 10 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0172others(7): Show | 11 | HG01123.hp2 HG01175.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.588+548dupA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112832012 | ||||||
chr7:112832176 | TAC | T | 1 | a0001c0001t0005g0006 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.588+383_588+384del others(2): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 4/4 | chr7 | 112832176 | ||||||
chr7:112832683 | CAG | C | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.474-10_474-9delCT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112832683 | ||||||
chr7:112832706 | C | G | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.474-31G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112832706 | ||||||
chr7:112832820 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.474-145C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112832820 | ||||||
chr7:112832984 | C | T | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-309G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112832984 | ||||||
chr7:112833530 | T | A | 4 | a0001c0002t0008g0002a0001c0002t0008g0034a0001c0002t0008g0036others(1): Show | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-855A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112833530 | ||||||
chr7:112833569 | G | T | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.474-894C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112833569 | ||||||
chr7:112833635 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.474-960T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112833635 | ||||||
chr7:112833646 | A | T | 13 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(10): Show | 15 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.474-971T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112833646 | ||||||
chr7:112834375 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.474-1700G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112834375 | ||||||
chr7:112834592 | C | G | 5 | a0001c0001t0009g0070a0001c0001t0009g0088a0001c0001t0009g0089others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-1917G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112834592 | ||||||
chr7:112834645 | C | T | 1 | a0001c0001t0003g0027 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.474-1970G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112834645 | ||||||
chr7:112834756 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-2081G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112834756 | ||||||
chr7:112834866 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.474-2191C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112834866 | ||||||
chr7:112835285 | A | G | 4 | a0001c0001t0004g0042a0001c0001t0004g0044a0001c0001t0004g0045others(1): Show | 4 | HG02572.hp2 HG03486.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-2610T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112835285 | ||||||
chr7:112835467 | C | T | 103 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0186others(100): Show | 106 | HG00099.hp1 HG00438.hp2 HG00673.hp2 others(103): Show |
intron_variant | MODIFIER | c.474-2792G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112835467 | ||||||
chr7:112835553 | G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG00438.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.474-2878C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112835553 | ||||||
chr7:112835578 | T | G | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.474-2903A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112835578 | ||||||
chr7:112835934 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-3259G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112835934 | ||||||
chr7:112835983 | T | A | 1 | a0001c0001t0005g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.474-3308A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112835983 | ||||||
chr7:112836115 | G | A | 4 | a0001c0002t0008g0002a0001c0002t0008g0034a0001c0002t0008g0036others(1): Show | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-3440C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112836115 | ||||||
chr7:112836469 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.474-3794G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112836469 | ||||||
chr7:112836700 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.474-4025G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112836700 | ||||||
chr7:112836701 | A | G | 122 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0186others(119): Show | 126 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.474-4026T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112836701 | ||||||
chr7:112837143 | G | A | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-4468C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112837143 | ||||||
chr7:112837360 | A | T | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-4685T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112837360 | ||||||
chr7:112837402 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-4727A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112837402 | ||||||
chr7:112837458 | G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.474-4783C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112837458 | ||||||
chr7:112837529 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-4854C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112837529 | ||||||
chr7:112837748 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.474-5073C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112837748 | ||||||
chr7:112837792 | G | A | 1 | a0001c0001t0007g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.474-5117C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112837792 | ||||||
chr7:112837874 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-5199G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112837874 | ||||||
chr7:112837943 | C | T | 1 | a0001c0001t0005g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.474-5268G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112837943 | ||||||
chr7:112838055 | A | G | 1 | a0001c0001t0002g0113 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.474-5380T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112838055 | ||||||
chr7:112838099 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.474-5424C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112838099 | ||||||
chr7:112838116 | C | T | 1 | a0001c0001t0006g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.474-5441G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112838116 | ||||||
chr7:112838397 | G | GAAAA | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-5726_474-5723d others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112838397 | ||||||
chr7:112838508 | T | G | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG02818.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-5833A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112838508 | ||||||
chr7:112838566 | C | T | 2 | a0001c0001t0002g0065a0001c0001t0002g0066 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.474-5891G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112838566 | ||||||
chr7:112838588 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-5913A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112838588 | ||||||
chr7:112838746 | C | CA | 5 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(2): Show | 5 | HG03098.hp2 NA18947.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-6072dupT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112838746 | ||||||
chr7:112838825 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.474-6150T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112838825 | ||||||
chr7:112838862 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.474-6187T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112838862 | ||||||
chr7:112839034 | A | G | 5 | a0001c0001t0009g0070a0001c0001t0009g0088a0001c0001t0009g0089others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-6359T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112839034 | ||||||
chr7:112839136 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.474-6461T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112839136 | ||||||
chr7:112839649 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-6974A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112839649 | ||||||
chr7:112839833 | A | G | 18 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(15): Show | 18 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.474-7158T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112839833 | ||||||
chr7:112839860 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.474-7185G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112839860 | ||||||
chr7:112839900 | A | ATACT | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-7229_474-7226d others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112839900 | ||||||
chr7:112840482 | C | T | 13 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(10): Show | 15 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.474-7807G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112840482 | ||||||
chr7:112840507 | A | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-7832T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112840507 | ||||||
chr7:112840587 | C | A | 1 | a0001c0001t0002g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.474-7912G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112840587 | ||||||
chr7:112840724 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.474-8049C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112840724 | ||||||
chr7:112840734 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-8059A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112840734 | ||||||
chr7:112840795 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.474-8120C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112840795 | ||||||
chr7:112840898 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.474-8223T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112840898 | ||||||
chr7:112840926 | CAT | C | 14 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0145others(11): Show | 14 | HG00438.hp1 HG00735.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.474-8253_474-8252d others(4): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112840926 | ||||||
chr7:112840928 | T | C | 1 | a0001c0002t0008g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.474-8253A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112840928 | ||||||
chr7:112841232 | C | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-8557G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112841232 | ||||||
chr7:112841241 | T | C | 4 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(1): Show | 4 | HG02723.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-8566A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112841241 | ||||||
chr7:112841378 | T | C | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-8703A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112841378 | ||||||
chr7:112841518 | T | A | 15 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.474-8843A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112841518 | ||||||
chr7:112841959 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.474-9284A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112841959 | ||||||
chr7:112842131 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-9456C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112842131 | ||||||
chr7:112842319 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-9644A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112842319 | ||||||
chr7:112842474 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-9799C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112842474 | ||||||
chr7:112842498 | T | G | 1 | a0001c0001t0001g0181 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.474-9823A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112842498 | ||||||
chr7:112842662 | G | A | 18 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(15): Show | 18 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.474-9987C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112842662 | ||||||
chr7:112842695 | A | G | 16 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0096others(13): Show | 17 | HG00438.hp2 HG00673.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.474-10020T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112842695 | ||||||
chr7:112842698 | T | C | 6 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-10023A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112842698 | ||||||
chr7:112842950 | A | C | 1 | a0001c0001t0004g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.474-10275T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112842950 | ||||||
chr7:112842956 | C | T | 111 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0186others(108): Show | 115 | HG00099.hp1 HG00438.hp2 HG00673.hp2 others(112): Show |
intron_variant | MODIFIER | c.474-10281G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112842956 | ||||||
chr7:112843036 | A | G | 33 | a0001c0001t0002g0003a0001c0001t0002g0065a0001c0001t0002g0066others(30): Show | 34 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.474-10361T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112843036 | ||||||
chr7:112843048 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-10373T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112843048 | ||||||
chr7:112843126 | T | C | 1 | a0001c0001t0004g0047 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.474-10451A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112843126 | ||||||
chr7:112843207 | C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0175 | 2 | HG01167.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.474-10532G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112843207 | ||||||
chr7:112843502 | G | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-10827C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112843502 | ||||||
chr7:112843551 | A | G | 18 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(15): Show | 18 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.474-10876T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112843551 | ||||||
chr7:112843630 | T | TA | 4 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(1): Show | 4 | HG02723.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-10956dupT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112843630 | ||||||
chr7:112843635 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.474-10960A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112843635 | ||||||
chr7:112843851 | T | G | 1 | a0001c0001t0001g0122 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.474-11176A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112843851 | ||||||
chr7:112843886 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-11211T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112843886 | ||||||
chr7:112843925 | C | A | 5 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(2): Show | 5 | HG02630.hp2 HG02818.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-11250G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112843925 | ||||||
chr7:112844320 | G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG01433.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.474-11645C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112844320 | ||||||
chr7:112844556 | T | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-11881A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112844556 | ||||||
chr7:112844724 | T | G | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-12049A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112844724 | ||||||
chr7:112844744 | AT | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-12070delA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112844744 | ||||||
chr7:112845072 | C | A | 1 | a0001c0001t0001g0185 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.474-12397G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112845072 | ||||||
chr7:112845482 | A | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-12807T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112845482 | ||||||
chr7:112845677 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.474-13002C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112845677 | ||||||
chr7:112845764 | C | T | 1 | a0001c0002t0008g0037 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.474-13089G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112845764 | ||||||
chr7:112845869 | G | T | 15 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.474-13194C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112845869 | ||||||
chr7:112845959 | T | C | 15 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.474-13284A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112845959 | ||||||
chr7:112846145 | C | CTTT | 4 | a0001c0002t0008g0002a0001c0002t0008g0034a0001c0002t0008g0036others(1): Show | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-13473_474-1347 others(7): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112846145 | ||||||
chr7:112846145 | C | CTTTTTTT | 15 | a0001c0001t0001g0074a0001c0001t0001g0186a0001c0001t0002g0116others(12): Show | 15 | HG01346.hp1 HG02486.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.474-13477_474-1347 others(11): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112846145 | ||||||
chr7:112846145 | C | CTTTTTTT others(1): Show |
61 | a0001c0001t0001g0075a0001c0001t0001g0187a0001c0001t0002g0003others(58): Show | 62 | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.474-13478_474-1347 others(12): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112846145 | ||||||
chr7:112846145 | C | CTTTTTTT others(2): Show |
14 | a0001c0001t0002g0100a0001c0001t0002g0107a0001c0001t0003g0022others(11): Show | 16 | HG00099.hp1 HG00438.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.474-13479_474-1347 others(13): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112846145 | ||||||
chr7:112846145 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0002g0101a0001c0001t0004g0039a0001c0001t0005g0190others(1): Show | 4 | HG01099.hp1 HG02886.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.474-13480_474-1347 others(14): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112846145 | ||||||
chr7:112846456 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-13781T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112846456 | ||||||
chr7:112846498 | A | C | 1 | a0001c0001t0002g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.474-13823T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112846498 | ||||||
chr7:112846785 | T | C | 13 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(10): Show | 15 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.474-14110A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112846785 | ||||||
chr7:112847434 | A | G | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | HG01975.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.474-14759T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112847434 | ||||||
chr7:112847683 | C | G | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.474-15008G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112847683 | ||||||
chr7:112847683 | C | T | 67 | a0001c0001t0001g0187a0001c0001t0002g0003a0001c0001t0002g0065others(64): Show | 68 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.474-15008G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112847683 | ||||||
chr7:112847710 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.474-15035C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112847710 | ||||||
chr7:112847765 | T | C | 116 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0186others(113): Show | 120 | HG00099.hp1 HG00438.hp2 HG00673.hp2 others(117): Show |
intron_variant | MODIFIER | c.474-15090A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112847765 | ||||||
chr7:112847771 | T | A | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.474-15096A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112847771 | ||||||
chr7:112847778 | C | CAAAAAAA others(12): Show |
5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-15104_474-1510 others(23): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112847778 | ||||||
chr7:112847853 | A | G | 1 | a0001c0001t0004g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.474-15178T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112847853 | ||||||
chr7:112847867 | G | A | 9 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(6): Show | 10 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.474-15192C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112847867 | ||||||
chr7:112848067 | C | T | 33 | a0001c0001t0002g0003a0001c0001t0002g0065a0001c0001t0002g0066others(30): Show | 34 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.474-15392G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112848067 | ||||||
chr7:112848193 | C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.474-15518G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112848193 | ||||||
chr7:112848232 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-15557C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112848232 | ||||||
chr7:112848327 | A | T | 3 | a0001c0001t0005g0006a0001c0001t0005g0189a0001c0001t0005g0192 | 4 | HG03490.hp2 HG03492.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.474-15652T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112848327 | ||||||
chr7:112848480 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-15805C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112848480 | ||||||
chr7:112848503 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.474-15828G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112848503 | ||||||
chr7:112848521 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-15846G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112848521 | ||||||
chr7:112848522 | G | A | 14 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0145others(11): Show | 14 | HG00438.hp1 HG00735.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.474-15847C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112848522 | ||||||
chr7:112848615 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.474-15940C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112848615 | ||||||
chr7:112848649 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-15974C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112848649 | ||||||
chr7:112848699 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-16024G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112848699 | ||||||
chr7:112848845 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.474-16170G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112848845 | ||||||
chr7:112848899 | A | G | 7 | a0001c0001t0001g0131a0001c0001t0001g0148a0001c0001t0001g0149others(4): Show | 7 | HG00735.hp1 HG01346.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.474-16224T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112848899 | ||||||
chr7:112848950 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.474-16275C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112848950 | ||||||
chr7:112849038 | G | T | 4 | a0001c0002t0008g0002a0001c0002t0008g0034a0001c0002t0008g0036others(1): Show | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-16363C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112849038 | ||||||
chr7:112849047 | T | TA | 105 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0158others(102): Show | 108 | HG00099.hp1 HG00438.hp2 HG00673.hp2 others(105): Show |
intron_variant | MODIFIER | c.474-16373dupT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112849047 | ||||||
chr7:112849047 | T | TAA | 7 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(4): Show | 7 | HG02258.hp2 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.474-16374_474-1637 others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112849047 | ||||||
chr7:112849081 | GTAC | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-16409_474-1640 others(7): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112849081 | ||||||
chr7:112849220 | T | C | 1 | a0001c0001t0005g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.474-16545A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112849220 | ||||||
chr7:112849544 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-16869T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112849544 | ||||||
chr7:112849852 | T | C | 5 | a0001c0001t0005g0005a0001c0001t0005g0195a0001c0001t0005g0196others(2): Show | 6 | HG01099.hp1 HG01258.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-17177A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112849852 | ||||||
chr7:112849872 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-17197T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112849872 | ||||||
chr7:112849895 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-17220A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112849895 | ||||||
chr7:112849906 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.474-17231A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112849906 | ||||||
chr7:112849986 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.474-17311G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112849986 | ||||||
chr7:112850157 | C | T | 69 | a0001c0001t0001g0075a0001c0001t0001g0187a0001c0001t0002g0003others(66): Show | 70 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.474-17482G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112850157 | ||||||
chr7:112850174 | C | G | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.474-17499G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112850174 | ||||||
chr7:112850203 | AAAC | A | 49 | a0001c0001t0002g0003a0001c0001t0002g0065a0001c0001t0002g0066others(46): Show | 50 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.474-17531_474-1752 others(7): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112850203 | ||||||
chr7:112850218 | C | A | 1 | a0001c0001t0004g0039 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.474-17543G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112850218 | ||||||
chr7:112850368 | G | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-17693C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112850368 | ||||||
chr7:112850517 | A | G | 1 | a0001c0001t0006g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.474-17842T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112850517 | ||||||
chr7:112851025 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-18350T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112851025 | ||||||
chr7:112851053 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-18378G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112851053 | ||||||
chr7:112851148 | C | G | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.474-18473G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112851148 | ||||||
chr7:112851212 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.474-18537A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112851212 | ||||||
chr7:112851263 | C | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-18588G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112851263 | ||||||
chr7:112851361 | C | T | 115 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0186others(112): Show | 119 | HG00099.hp1 HG00438.hp2 HG00673.hp2 others(116): Show |
intron_variant | MODIFIER | c.474-18686G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112851361 | ||||||
chr7:112851616 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-18941A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112851616 | ||||||
chr7:112851644 | C | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-18969G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112851644 | ||||||
chr7:112851686 | C | T | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.474-19011G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112851686 | ||||||
chr7:112851761 | T | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-19086A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112851761 | ||||||
chr7:112851848 | AACAG | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-19177_474-1917 others(8): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112851848 | ||||||
chr7:112852238 | T | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-19563A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112852238 | ||||||
chr7:112852244 | A | G | 4 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(1): Show | 4 | HG02723.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-19569T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112852244 | ||||||
chr7:112852257 | C | A | 67 | a0001c0001t0001g0187a0001c0001t0002g0003a0001c0001t0002g0065others(64): Show | 68 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.474-19582G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112852257 | ||||||
chr7:112852275 | G | A | 12 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(9): Show | 14 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.474-19600C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112852275 | ||||||
chr7:112852280 | C | A | 1 | a0001c0001t0001g0187 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.474-19605G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112852280 | ||||||
chr7:112852297 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-19622G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112852297 | ||||||
chr7:112852325 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.474-19650C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112852325 | ||||||
chr7:112852429 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474-19754A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112852429 | ||||||
chr7:112852593 | A | AAAT | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-19921_474-1991 others(7): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112852593 | ||||||
chr7:112852650 | A | G | 1 | a0001c0001t0009g0070 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.474-19975T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112852650 | ||||||
chr7:112852699 | G | A | 1 | a0001c0002t0003g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.474-20024C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112852699 | ||||||
chr7:112852912 | A | G | 1 | a0001c0001t0005g0192 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.474-20237T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112852912 | ||||||
chr7:112852926 | ACT | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-20253_474-2025 others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112852926 | ||||||
chr7:112852933 | C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0175 | 2 | HG01167.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.474-20258G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112852933 | ||||||
chr7:112852941 | A | T | 1 | a0001c0001t0001g0142 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.474-20266T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112852941 | ||||||
chr7:112853091 | T | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-20416A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112853091 | ||||||
chr7:112853168 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-20493G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112853168 | ||||||
chr7:112853194 | T | C | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.474-20519A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112853194 | ||||||
chr7:112853224 | A | AGAATTTA others(5): Show |
194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(191): Show | 201 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.474-20550_474-2054 others(16): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112853224 | ||||||
chr7:112853262 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-20587C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112853262 | ||||||
chr7:112853522 | C | T | 15 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.474-20847G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112853522 | ||||||
chr7:112853655 | T | C | 1 | a0001c0001t0010g0103 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.474-20980A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112853655 | ||||||
chr7:112853843 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.474-21168T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112853843 | ||||||
chr7:112853868 | C | A | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.474-21193G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112853868 | ||||||
chr7:112854078 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.474-21403A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112854078 | ||||||
chr7:112854084 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.474-21409G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112854084 | ||||||
chr7:112854372 | G | C | 18 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(15): Show | 18 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.474-21697C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112854372 | ||||||
chr7:112854600 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.474-21925T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112854600 | ||||||
chr7:112854746 | A | G | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.474-22071T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112854746 | ||||||
chr7:112854773 | A | G | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.474-22098T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112854773 | ||||||
chr7:112854823 | T | C | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG01891.hp2 HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.474-22148A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112854823 | ||||||
chr7:112854870 | A | G | 3 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0082 | 3 | HG02258.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.474-22195T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112854870 | ||||||
chr7:112855111 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.474-22436A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112855111 | ||||||
chr7:112855172 | T | C | 4 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(1): Show | 4 | HG02723.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-22497A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112855172 | ||||||
chr7:112855184 | C | G | 1 | a0001c0001t0005g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.474-22509G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112855184 | ||||||
chr7:112855249 | C | A | 1 | a0001c0002t0008g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.474-22574G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112855249 | ||||||
chr7:112855356 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-22681G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112855356 | ||||||
chr7:112855472 | T | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-22797A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112855472 | ||||||
chr7:112855483 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-22808A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112855483 | ||||||
chr7:112855626 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-22951C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112855626 | ||||||
chr7:112855789 | T | G | 1 | a0001c0002t0003g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.474-23114A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112855789 | ||||||
chr7:112855908 | TA | T | 9 | a0001c0001t0001g0179a0001c0001t0002g0065a0001c0001t0002g0066others(6): Show | 9 | HG02486.hp2 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-23234delT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112855908 | ||||||
chr7:112855950 | T | G | 5 | a0001c0001t0013g0038a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-23275A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112855950 | ||||||
chr7:112856060 | A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(195): Show | 205 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.474-23385T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112856060 | ||||||
chr7:112856157 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.474-23482G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112856157 | ||||||
chr7:112856254 | CTT | C | 4 | a0001c0002t0008g0002a0001c0002t0008g0034a0001c0002t0008g0036others(1): Show | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-23581_474-2358 others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112856254 | ||||||
chr7:112856501 | C | T | 15 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.474-23826G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112856501 | ||||||
chr7:112856733 | AT | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-24059delA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112856733 | ||||||
chr7:112857020 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-24345A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112857020 | ||||||
chr7:112857065 | AATGTTCT others(318): Show |
A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-24715_474-2439 others(4): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112857065 | ||||||
chr7:112857079 | C | CT | 23 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0159others(20): Show | 23 | HG01168.hp1 HG01243.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.474-24405dupA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112857079 | ||||||
chr7:112857079 | CT | C | 14 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0150others(11): Show | 14 | HG02630.hp2 HG02818.hp1 HG02965.hp1 others(11): Show |
intron_variant | MODIFIER | c.474-24405delA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112857079 | ||||||
chr7:112857237 | G | A | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.474-24562C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112857237 | ||||||
chr7:112857313 | A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(189): Show | 198 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.474-24638T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112857313 | ||||||
chr7:112857342 | C | T | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.474-24667G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112857342 | ||||||
chr7:112857351 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.474-24676T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112857351 | ||||||
chr7:112857606 | A | G | 1 | a0001c0001t0006g0064 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.474-24931T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112857606 | ||||||
chr7:112857670 | T | C | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-24995A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112857670 | ||||||
chr7:112857681 | G | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-25006C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112857681 | ||||||
chr7:112858107 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.474-25432G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112858107 | ||||||
chr7:112858495 | T | TG | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-25821_474-2582 others(5): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112858495 | ||||||
chr7:112858550 | CTTAT | C | 6 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(3): Show | 6 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-25879_474-2587 others(8): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112858550 | ||||||
chr7:112858734 | C | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-26059G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112858734 | ||||||
chr7:112858844 | C | A | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-26169G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112858844 | ||||||
chr7:112858956 | G | A | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.474-26281C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112858956 | ||||||
chr7:112859200 | G | T | 18 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(15): Show | 18 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.474-26525C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112859200 | ||||||
chr7:112859226 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.474-26551T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112859226 | ||||||
chr7:112859374 | G | A | 3 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0188 | 3 | HG01168.hp2 HG01346.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.474-26699C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112859374 | ||||||
chr7:112859667 | ATG | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-26994_474-2699 others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112859667 | ||||||
chr7:112859703 | A | C | 2 | a0001c0001t0006g0085a0001c0001t0006g0086 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.474-27028T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112859703 | ||||||
chr7:112859869 | C | T | 111 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0186others(108): Show | 115 | HG00099.hp1 HG00438.hp2 HG00673.hp2 others(112): Show |
intron_variant | MODIFIER | c.474-27194G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112859869 | ||||||
chr7:112859933 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.474-27258T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112859933 | ||||||
chr7:112860359 | C | T | 1 | a0001c0001t0009g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.474-27684G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112860359 | ||||||
chr7:112860406 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-27731C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112860406 | ||||||
chr7:112860540 | C | T | 1 | a0001c0001t0009g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-27865G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112860540 | ||||||
chr7:112860626 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-27951C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112860626 | ||||||
chr7:112860628 | C | T | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.474-27953G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112860628 | ||||||
chr7:112860737 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-28062T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112860737 | ||||||
chr7:112860805 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.474-28130C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112860805 | ||||||
chr7:112860861 | G | A | 2 | a0001c0001t0002g0079a0001c0001t0002g0083 | 2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.474-28186C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112860861 | ||||||
chr7:112860892 | G | A | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-28217C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112860892 | ||||||
chr7:112860912 | C | CA | 55 | a0001c0001t0001g0004a0001c0001t0001g0075a0001c0001t0001g0118others(52): Show | 57 | HG00438.hp1 HG00673.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.474-28238dupT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112860912 | ||||||
chr7:112861065 | C | T | 1 | a0001c0001t0002g0101 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.474-28390G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112861065 | ||||||
chr7:112861070 | G | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0168 | 2 | HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.474-28395C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112861070 | ||||||
chr7:112861130 | TATA | T | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-28458_474-2845 others(7): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112861130 | ||||||
chr7:112861505 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-28830C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112861505 | ||||||
chr7:112861507 | T | C | 1 | a0001c0002t0003g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.474-28832A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112861507 | ||||||
chr7:112861778 | G | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG01891.hp2 HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.474-29103C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112861778 | ||||||
chr7:112861826 | C | T | 97 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0186others(94): Show | 100 | HG00099.hp1 HG00438.hp2 HG00673.hp2 others(97): Show |
intron_variant | MODIFIER | c.474-29151G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112861826 | ||||||
chr7:112861855 | CTTTG | C | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-29184_474-2918 others(8): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112861855 | ||||||
chr7:112861921 | C | G | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG01106.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.474-29246G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112861921 | ||||||
chr7:112862214 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.474-29539G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112862214 | ||||||
chr7:112862334 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-29659G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112862334 | ||||||
chr7:112862338 | G | A | 1 | a0001c0001t0010g0105 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.474-29663C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112862338 | ||||||
chr7:112862408 | T | C | 7 | a0001c0001t0002g0110a0001c0001t0002g0112a0001c0001t0002g0113others(4): Show | 7 | HG00738.hp2 HG01167.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-29733A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112862408 | ||||||
chr7:112862488 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-29813T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112862488 | ||||||
chr7:112862645 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-29970A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112862645 | ||||||
chr7:112862908 | G | A | 3 | a0001c0001t0005g0190a0001c0001t0005g0191a0001c0001t0010g0104 | 3 | HG03239.hp1 HG04199.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.474-30233C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112862908 | ||||||
chr7:112862923 | C | CA | 46 | a0001c0001t0001g0004a0001c0001t0001g0055a0001c0001t0001g0056others(43): Show | 48 | HG00673.hp1 HG00733.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.474-30249dupT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112862923 | ||||||
chr7:112863222 | G | C | 1 | a0001c0001t0012g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.474-30547C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112863222 | ||||||
chr7:112863272 | A | G | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.474-30597T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112863272 | ||||||
chr7:112863783 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-31108C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112863783 | ||||||
chr7:112863817 | C | T | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.474-31142G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112863817 | ||||||
chr7:112863822 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.474-31147T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112863822 | ||||||
chr7:112863990 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.474-31315C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112863990 | ||||||
chr7:112864226 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+31343A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112864226 | ||||||
chr7:112864312 | A | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(84): Show | 90 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.473+31257T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112864312 | ||||||
chr7:112864348 | A | G | 1 | a0001c0001t0002g0094 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.473+31221T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112864348 | ||||||
chr7:112864581 | G | A | 1 | a0001c0001t0005g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.473+30988C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112864581 | ||||||
chr7:112864686 | G | A | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+30883C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112864686 | ||||||
chr7:112864699 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.473+30870C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112864699 | ||||||
chr7:112864705 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.473+30864C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112864705 | ||||||
chr7:112864804 | G | A | 1 | a0001c0001t0005g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.473+30765C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112864804 | ||||||
chr7:112864848 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.473+30721C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112864848 | ||||||
chr7:112864966 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.473+30603G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112864966 | ||||||
chr7:112864997 | G | A | 1 | a0001c0001t0012g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.473+30572C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112864997 | ||||||
chr7:112865222 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.473+30347C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865222 | ||||||
chr7:112865404 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.473+30165T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865404 | ||||||
chr7:112865422 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.473+30147G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865422 | ||||||
chr7:112865426 | C | A | 1 | a0001c0001t0006g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.473+30143G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865426 | ||||||
chr7:112865533 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+30036G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865533 | ||||||
chr7:112865556 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+30013C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865556 | ||||||
chr7:112865596 | T | C | 1 | a0001c0001t0003g0019 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.473+29973A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865596 | ||||||
chr7:112865610 | A | C | 5 | a0001c0001t0009g0070a0001c0001t0009g0088a0001c0001t0009g0089others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+29959T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865610 | ||||||
chr7:112865632 | A | ATATATTT others(57): Show |
1 | a0001c0001t0001g0157 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.473+29936_473+2993 others(68): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865632 | ||||||
chr7:112865632 | A | ATATTTCA others(55): Show |
3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG01891.hp2 HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.473+29936_473+2993 others(66): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865632 | ||||||
chr7:112865638 | T | C | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+29931A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865638 | ||||||
chr7:112865657 | A | AT | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+29911dupA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865657 | ||||||
chr7:112865659 | A | ACATATAT others(68): Show |
1 | a0001c0001t0001g0122 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.473+29909_473+2991 others(79): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865659 | ||||||
chr7:112865659 | A | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+29910T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865659 | ||||||
chr7:112865667 | C | CATACATA others(23): Show |
83 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(80): Show | 86 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.473+29901_473+2990 others(34): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865667 | ||||||
chr7:112865667 | C | T | 15 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0129others(12): Show | 16 | HG01192.hp2 HG01891.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.473+29902G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865667 | ||||||
chr7:112865686 | A | ATTT | 87 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0179others(84): Show | 88 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.473+29880_473+2988 others(7): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865686 | ||||||
chr7:112865698 | CATAT | C | 15 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.473+29867_473+2987 others(8): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865698 | ||||||
chr7:112865706 | C | CAT | 3 | a0001c0002t0008g0002a0001c0002t0008g0036a0001c0002t0008g0037 | 4 | HG01192.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.473+29861_473+2986 others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865706 | ||||||
chr7:112865711 | AT | A | 2 | a0001c0002t0003g0035a0001c0002t0008g0034 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.473+29857delA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865711 | ||||||
chr7:112865730 | A | ATTCATAT others(6): Show |
3 | a0001c0002t0008g0002a0001c0002t0008g0036a0001c0002t0008g0037 | 4 | HG01192.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.473+29838_473+2983 others(17): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865730 | ||||||
chr7:112865733 | C | CAT | 2 | a0001c0002t0003g0035a0001c0002t0008g0034 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.473+29834_473+2983 others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865733 | ||||||
chr7:112865769 | A | ATTTCATA others(416): Show |
3 | a0001c0002t0008g0002a0001c0002t0008g0036a0001c0002t0008g0037 | 4 | HG01192.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.473+29799_473+2980 others(427): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865769 | ||||||
chr7:112865769 | A | ATTTCATA others(487): Show |
3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069 | 3 | HG01975.hp1 HG02809.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.473+29799_473+2980 others(498): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865769 | ||||||
chr7:112865769 | A | ATTTCATA others(434): Show |
2 | a0001c0001t0002g0065a0001c0001t0002g0066 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.473+29799_473+2980 others(445): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865769 | ||||||
chr7:112865769 | A | ATTTCATA others(456): Show |
2 | a0001c0002t0003g0035a0001c0002t0008g0034 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.473+29799_473+2980 others(467): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865769 | ||||||
chr7:112865912 | T | C | 1 | a0001c0001t0003g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.473+29657A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865912 | ||||||
chr7:112865936 | C | A | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+29633G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112865936 | ||||||
chr7:112866097 | A | G | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+29472T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112866097 | ||||||
chr7:112866316 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.473+29253A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112866316 | ||||||
chr7:112866389 | T | C | 1 | a0001c0001t0001g0184 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.473+29180A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112866389 | ||||||
chr7:112866487 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.473+29082T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112866487 | ||||||
chr7:112866548 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.473+29021C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112866548 | ||||||
chr7:112866666 | C | T | 15 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.473+28903G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112866666 | ||||||
chr7:112867232 | T | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(79): Show | 85 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.473+28337A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112867232 | ||||||
chr7:112867396 | ATAAT | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+28169_473+2817 others(8): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112867396 | ||||||
chr7:112867551 | A | G | 2 | a0001c0001t0007g0009a0001c0001t0007g0012 | 2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.473+28018T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112867551 | ||||||
chr7:112867651 | T | C | 1 | a0001c0001t0005g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.473+27918A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112867651 | ||||||
chr7:112867652 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.473+27917C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112867652 | ||||||
chr7:112867836 | C | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0102others(1): Show | 5 | HG01123.hp1 HG01358.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+27733G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112867836 | ||||||
chr7:112867900 | C | A | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+27669G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112867900 | ||||||
chr7:112868243 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+27326G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112868243 | ||||||
chr7:112868586 | C | T | 6 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(3): Show | 6 | HG01168.hp1 HG02258.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.473+26983G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112868586 | ||||||
chr7:112868939 | C | T | 6 | a0001c0001t0006g0059a0001c0001t0006g0060a0001c0001t0006g0061others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+26630G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112868939 | ||||||
chr7:112868954 | G | A | 1 | a0001c0001t0005g0006 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.473+26615C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112868954 | ||||||
chr7:112868962 | C | A | 1 | a0001c0001t0007g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.473+26607G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112868962 | ||||||
chr7:112868967 | C | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+26602G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112868967 | ||||||
chr7:112869153 | G | A | 5 | a0001c0001t0009g0070a0001c0001t0009g0088a0001c0001t0009g0089others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+26416C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112869153 | ||||||
chr7:112869157 | A | AG | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+26411dupC | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112869157 | ||||||
chr7:112869159 | T | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+26410A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112869159 | ||||||
chr7:112869206 | G | A | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0137 | 3 | HG00673.hp1 HG01192.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.473+26363C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112869206 | ||||||
chr7:112869211 | C | T | 1 | a0001c0002t0003g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.473+26358G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112869211 | ||||||
chr7:112869370 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+26199G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112869370 | ||||||
chr7:112869425 | C | T | 1 | a0001c0001t0005g0006 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.473+26144G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112869425 | ||||||
chr7:112869565 | TA | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+26003delT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112869565 | ||||||
chr7:112869743 | G | A | 3 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0082 | 3 | HG02258.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.473+25826C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112869743 | ||||||
chr7:112869879 | T | C | 1 | a0001c0001t0002g0117 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.473+25690A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112869879 | ||||||
chr7:112870011 | G | T | 6 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+25558C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112870011 | ||||||
chr7:112870082 | G | T | 28 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0094others(25): Show | 29 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.473+25487C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112870082 | ||||||
chr7:112870243 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.473+25326A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112870243 | ||||||
chr7:112870626 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.473+24943G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112870626 | ||||||
chr7:112870750 | T | TA | 14 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(11): Show | 14 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.473+24818dupT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112870750 | ||||||
chr7:112870750 | TA | T | 9 | a0001c0001t0001g0180a0001c0001t0002g0065a0001c0001t0002g0066others(6): Show | 9 | HG00099.hp1 HG00738.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.473+24818delT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112870750 | ||||||
chr7:112870750 | TAAA | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+24816_473+2481 others(7): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112870750 | ||||||
chr7:112870808 | TAC | T | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.473+24759_473+2476 others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112870808 | ||||||
chr7:112870903 | C | T | 16 | a0001c0001t0004g0039a0001c0001t0004g0040a0001c0001t0004g0041others(13): Show | 16 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.473+24666G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112870903 | ||||||
chr7:112870935 | A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0182 | 2 | HG02040.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.473+24634T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112870935 | ||||||
chr7:112870941 | C | T | 4 | a0001c0002t0008g0002a0001c0002t0008g0034a0001c0002t0008g0036others(1): Show | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+24628G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112870941 | ||||||
chr7:112871435 | T | G | 1 | a0001c0001t0004g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.473+24134A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112871435 | ||||||
chr7:112871445 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.473+24124C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112871445 | ||||||
chr7:112871453 | C | CA | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+24115dupT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112871453 | ||||||
chr7:112871701 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+23868G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112871701 | ||||||
chr7:112871736 | C | CAGACCAC others(11): Show |
15 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.473+23815_473+2383 others(22): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112871736 | ||||||
chr7:112871739 | A | C | 1 | a0001c0001t0002g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.473+23830T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112871739 | ||||||
chr7:112871766 | TAAAC | T | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.473+23799_473+2380 others(8): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112871766 | ||||||
chr7:112871823 | T | C | 4 | a0001c0002t0008g0002a0001c0002t0008g0034a0001c0002t0008g0036others(1): Show | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+23746A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112871823 | ||||||
chr7:112871832 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+23737G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112871832 | ||||||
chr7:112871865 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+23704G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112871865 | ||||||
chr7:112871945 | G | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 12 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.473+23624C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112871945 | ||||||
chr7:112872027 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.473+23542C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112872027 | ||||||
chr7:112872084 | C | A | 1 | a0001c0001t0009g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.473+23485G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112872084 | ||||||
chr7:112872278 | ATGAT | A | 4 | a0001c0002t0008g0002a0001c0002t0008g0034a0001c0002t0008g0036others(1): Show | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+23287_473+2329 others(8): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112872278 | ||||||
chr7:112872429 | T | C | 17 | a0001c0001t0003g0026a0001c0001t0004g0039a0001c0001t0004g0040others(14): Show | 17 | HG01243.hp2 HG02280.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.473+23140A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112872429 | ||||||
chr7:112872805 | T | TA | 7 | a0001c0001t0001g0151a0001c0001t0005g0006a0001c0001t0005g0189others(4): Show | 9 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.473+22763dupT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112872805 | ||||||
chr7:112872856 | A | G | 15 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.473+22713T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112872856 | ||||||
chr7:112873463 | G | T | 1 | a0001c0001t0006g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.473+22106C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112873463 | ||||||
chr7:112873485 | A | T | 1 | a0001c0001t0001g0162 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.473+22084T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112873485 | ||||||
chr7:112873539 | C | A | 3 | a0001c0001t0004g0042a0001c0001t0004g0044a0001c0001t0004g0045 | 3 | HG02572.hp2 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.473+22030G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112873539 | ||||||
chr7:112873713 | T | C | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.473+21856A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112873713 | ||||||
chr7:112873877 | T | C | 10 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(7): Show | 11 | HG01192.hp2 HG01975.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.473+21692A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112873877 | ||||||
chr7:112874067 | C | T | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+21502G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112874067 | ||||||
chr7:112874179 | T | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+21390A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112874179 | ||||||
chr7:112874326 | G | C | 63 | a0001c0001t0001g0118a0001c0001t0001g0187a0001c0001t0002g0003others(60): Show | 64 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.473+21243C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112874326 | ||||||
chr7:112874396 | A | G | 1 | a0001c0001t0003g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.473+21173T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112874396 | ||||||
chr7:112874723 | A | AAAAAC | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+20845_473+2084 others(9): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112874723 | ||||||
chr7:112874724 | T | A | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+20845A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112874724 | ||||||
chr7:112874725 | C | G | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+20844G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112874725 | ||||||
chr7:112874726 | T | A | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+20843A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112874726 | ||||||
chr7:112874728 | G | A | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+20841C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112874728 | ||||||
chr7:112874780 | A | G | 1 | a0001c0001t0003g0022 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.473+20789T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112874780 | ||||||
chr7:112874846 | C | A | 4 | a0001c0002t0008g0002a0001c0002t0008g0034a0001c0002t0008g0036others(1): Show | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+20723G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112874846 | ||||||
chr7:112874864 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+20705C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112874864 | ||||||
chr7:112874955 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+20614A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112874955 | ||||||
chr7:112874990 | G | T | 12 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(9): Show | 14 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.473+20579C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112874990 | ||||||
chr7:112875034 | G | A | 4 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(1): Show | 4 | HG02723.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+20535C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112875034 | ||||||
chr7:112875052 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+20517C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112875052 | ||||||
chr7:112875301 | G | A | 4 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(1): Show | 4 | HG02723.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+20268C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112875301 | ||||||
chr7:112875641 | G | A | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.473+19928C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112875641 | ||||||
chr7:112875724 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.473+19845G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112875724 | ||||||
chr7:112875844 | T | C | 6 | a0001c0001t0006g0059a0001c0001t0006g0060a0001c0001t0006g0061others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+19725A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112875844 | ||||||
chr7:112875873 | CTCTT | C | 3 | a0001c0001t0011g0071a0001c0001t0011g0072a0001c0001t0011g0073 | 3 | NA18950.hp1 NA19060.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.473+19692_473+1969 others(8): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112875873 | ||||||
chr7:112876088 | G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(185): Show | 194 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.473+19481C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112876088 | ||||||
chr7:112876122 | G | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+19447C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112876122 | ||||||
chr7:112876285 | TTC | T | 15 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.473+19282_473+1928 others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112876285 | ||||||
chr7:112876922 | A | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0127a0001c0001t0001g0128others(32): Show | 37 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.473+18647T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112876922 | ||||||
chr7:112877397 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.473+18172G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112877397 | ||||||
chr7:112877543 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+18026A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112877543 | ||||||
chr7:112877656 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.473+17913G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112877656 | ||||||
chr7:112877678 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+17891A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112877678 | ||||||
chr7:112877759 | A | C | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.473+17810T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112877759 | ||||||
chr7:112877769 | TCTTGTGA others(3): Show |
T | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+17790_473+1779 others(14): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112877769 | ||||||
chr7:112877771 | T | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(79): Show | 85 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.473+17798A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112877771 | ||||||
chr7:112878069 | G | C | 7 | a0001c0001t0003g0016a0001c0001t0007g0007a0001c0001t0007g0008others(4): Show | 7 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.473+17500C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112878069 | ||||||
chr7:112878302 | G | T | 2 | a0001c0001t0002g0099a0001c0001t0002g0121 | 2 | NA18970.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.473+17267C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112878302 | ||||||
chr7:112878434 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.473+17135C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112878434 | ||||||
chr7:112878461 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.473+17108G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112878461 | ||||||
chr7:112878561 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+17008C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112878561 | ||||||
chr7:112878617 | G | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+16952C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112878617 | ||||||
chr7:112878725 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.473+16844C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112878725 | ||||||
chr7:112879083 | G | A | 2 | a0001c0001t0006g0085a0001c0001t0006g0086 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.473+16486C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112879083 | ||||||
chr7:112879296 | G | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+16273C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112879296 | ||||||
chr7:112879315 | C | T | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+16254G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112879315 | ||||||
chr7:112879356 | G | C | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+16213C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112879356 | ||||||
chr7:112879542 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+16027G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112879542 | ||||||
chr7:112879599 | A | G | 4 | a0001c0001t0010g0103a0001c0001t0010g0104a0001c0001t0010g0105others(1): Show | 4 | HG00673.hp2 HG02056.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+15970T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112879599 | ||||||
chr7:112879673 | CAT | C | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.473+15894_473+1589 others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112879673 | ||||||
chr7:112879677 | T | C | 1 | a0001c0002t0003g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.473+15892A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112879677 | ||||||
chr7:112879765 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+15804G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112879765 | ||||||
chr7:112880251 | C | T | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.473+15318G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112880251 | ||||||
chr7:112880438 | T | C | 10 | a0001c0001t0002g0096a0001c0001t0002g0099a0001c0001t0002g0100others(7): Show | 10 | HG00438.hp2 HG00673.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.473+15131A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112880438 | ||||||
chr7:112880441 | C | T | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+15128G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112880441 | ||||||
chr7:112880454 | AC | A | 5 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(2): Show | 5 | HG02922.hp2 NA18947.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+15114delG | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112880454 | ||||||
chr7:112880547 | G | T | 1 | a0001c0001t0004g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.473+15022C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112880547 | ||||||
chr7:112880898 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.473+14671C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112880898 | ||||||
chr7:112880917 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+14652T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112880917 | ||||||
chr7:112880963 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+14606A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112880963 | ||||||
chr7:112881093 | G | C | 8 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0112others(5): Show | 8 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.473+14476C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112881093 | ||||||
chr7:112881134 | C | T | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+14435G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112881134 | ||||||
chr7:112881227 | A | G | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.473+14342T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112881227 | ||||||
chr7:112881232 | C | T | 18 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(15): Show | 18 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.473+14337G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112881232 | ||||||
chr7:112881290 | G | C | 4 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0022others(1): Show | 4 | HG01496.hp1 HG02622.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+14279C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112881290 | ||||||
chr7:112881349 | T | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG01346.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.473+14220A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112881349 | ||||||
chr7:112881349 | T | G | 1 | a0001c0001t0004g0039 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.473+14220A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112881349 | ||||||
chr7:112881513 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.473+14056G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112881513 | ||||||
chr7:112881566 | G | T | 4 | a0001c0001t0006g0060a0001c0001t0006g0061a0001c0001t0006g0062others(1): Show | 4 | HG02486.hp1 HG02615.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.473+14003C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112881566 | ||||||
chr7:112881875 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.473+13694C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112881875 | ||||||
chr7:112881910 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.473+13659C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112881910 | ||||||
chr7:112881936 | G | A | 1 | a0001c0001t0005g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.473+13633C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112881936 | ||||||
chr7:112882141 | C | T | 63 | a0001c0001t0001g0075a0001c0001t0001g0187a0001c0001t0002g0003others(60): Show | 64 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.473+13428G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112882141 | ||||||
chr7:112882450 | G | A | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.473+13119C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112882450 | ||||||
chr7:112882459 | G | A | 1 | a0001c0001t0012g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.473+13110C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112882459 | ||||||
chr7:112882487 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+13082C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112882487 | ||||||
chr7:112882766 | T | A | 1 | a0001c0001t0002g0068 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.473+12803A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112882766 | ||||||
chr7:112882766 | TA | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(142): Show | 151 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.473+12802delT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112882766 | ||||||
chr7:112882766 | TAA | T | 31 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0148others(28): Show | 32 | HG00735.hp1 HG01099.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.473+12801_473+1280 others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112882766 | ||||||
chr7:112882767 | A | T | 10 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(7): Show | 10 | HG00639.hp2 HG01175.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.473+12802T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112882767 | ||||||
chr7:112882768 | A | T | 116 | a0001c0001t0001g0004a0001c0001t0001g0074a0001c0001t0001g0075others(113): Show | 120 | HG00099.hp1 HG00438.hp2 HG00673.hp1 others(117): Show |
intron_variant | MODIFIER | c.473+12801T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112882768 | ||||||
chr7:112882769 | A | T | 23 | a0001c0001t0001g0126a0001c0001t0001g0164a0001c0001t0001g0183others(20): Show | 24 | HG01099.hp1 HG01167.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.473+12800T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112882769 | ||||||
chr7:112882770 | A | T | 3 | a0001c0001t0002g0084a0001c0002t0003g0035a0001c0002t0008g0036 | 3 | HG01168.hp1 HG01192.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.473+12799T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112882770 | ||||||
chr7:112882882 | G | A | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+12687C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112882882 | ||||||
chr7:112882914 | A | C | 1 | a0001c0001t0002g0100 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.473+12655T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112882914 | ||||||
chr7:112883285 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.473+12284G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112883285 | ||||||
chr7:112883460 | A | G | 1 | a0001c0001t0004g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.473+12109T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112883460 | ||||||
chr7:112883853 | C | T | 12 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(9): Show | 14 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.473+11716G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112883853 | ||||||
chr7:112883918 | C | T | 2 | a0001c0001t0003g0016a0001c0001t0013g0038 | 2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.473+11651G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112883918 | ||||||
chr7:112884055 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.473+11514C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112884055 | ||||||
chr7:112884135 | A | C | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.473+11434T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112884135 | ||||||
chr7:112884467 | G | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+11102C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112884467 | ||||||
chr7:112884542 | G | A | 13 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(10): Show | 15 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.473+11027C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112884542 | ||||||
chr7:112884658 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.473+10911A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112884658 | ||||||
chr7:112884756 | G | T | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+10813C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112884756 | ||||||
chr7:112884829 | A | C | 1 | a0001c0001t0003g0022 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.473+10740T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112884829 | ||||||
chr7:112885091 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+10478G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112885091 | ||||||
chr7:112885167 | AG | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0056others(160): Show | 169 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.473+10401delC | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112885167 | ||||||
chr7:112885474 | C | G | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+10095G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112885474 | ||||||
chr7:112885741 | C | G | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.473+9828G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112885741 | ||||||
chr7:112885831 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+9738T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112885831 | ||||||
chr7:112886029 | C | T | 1 | a0001c0001t0012g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.473+9540G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112886029 | ||||||
chr7:112886126 | C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0158 | 2 | HG02056.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.473+9443G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112886126 | ||||||
chr7:112886536 | A | G | 2 | a0001c0001t0005g0190a0001c0001t0005g0191 | 2 | HG03239.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.473+9033T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112886536 | ||||||
chr7:112886665 | T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0182 | 2 | HG02040.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.473+8904A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112886665 | ||||||
chr7:112886782 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.473+8787G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112886782 | ||||||
chr7:112886785 | A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(190): Show | 200 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.473+8784T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112886785 | ||||||
chr7:112886909 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.473+8660C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112886909 | ||||||
chr7:112886971 | C | T | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+8598G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112886971 | ||||||
chr7:112887259 | A | G | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+8310T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112887259 | ||||||
chr7:112887487 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.473+8082A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112887487 | ||||||
chr7:112887531 | C | T | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+8038G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112887531 | ||||||
chr7:112887840 | G | A | 1 | a0001c0001t0004g0043 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.473+7729C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112887840 | ||||||
chr7:112887841 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+7728A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112887841 | ||||||
chr7:112888038 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.473+7531G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112888038 | ||||||
chr7:112888053 | C | CAT | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+7515_473+7516i others(4): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112888053 | ||||||
chr7:112888063 | A | G | 5 | a0001c0001t0007g0008a0001c0001t0007g0009a0001c0001t0007g0010others(2): Show | 5 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+7506T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112888063 | ||||||
chr7:112888190 | G | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+7379C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112888190 | ||||||
chr7:112888310 | T | C | 15 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.473+7259A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112888310 | ||||||
chr7:112888497 | T | C | 1 | a0001c0001t0005g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.473+7072A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112888497 | ||||||
chr7:112888541 | T | C | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.473+7028A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112888541 | ||||||
chr7:112888552 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+7017G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112888552 | ||||||
chr7:112888578 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+6991C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112888578 | ||||||
chr7:112888690 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+6879C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112888690 | ||||||
chr7:112888865 | G | C | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.473+6704C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112888865 | ||||||
chr7:112888895 | G | C | 1 | a0001c0001t0002g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.473+6674C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112888895 | ||||||
chr7:112888939 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+6630G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112888939 | ||||||
chr7:112889385 | C | T | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.473+6184G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112889385 | ||||||
chr7:112889610 | A | T | 2 | a0001c0001t0004g0053a0001c0001t0004g0054 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.473+5959T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112889610 | ||||||
chr7:112889758 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+5811G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112889758 | ||||||
chr7:112889799 | G | A | 17 | a0001c0001t0001g0074a0001c0001t0005g0005a0001c0001t0005g0006others(14): Show | 19 | HG00099.hp1 HG01258.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.473+5770C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112889799 | ||||||
chr7:112889812 | C | G | 1 | a0001c0001t0002g0113 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.473+5757G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112889812 | ||||||
chr7:112890186 | A | G | 1 | a0001c0001t0009g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.473+5383T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112890186 | ||||||
chr7:112890368 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+5201G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112890368 | ||||||
chr7:112890370 | CACCTCTG others(6): Show |
C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+5186_473+5198d others(15): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112890370 | ||||||
chr7:112890468 | GA | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+5100delT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112890468 | ||||||
chr7:112890569 | T | C | 6 | a0001c0001t0002g0096a0001c0001t0002g0099a0001c0001t0002g0100others(3): Show | 6 | HG00438.hp2 HG02027.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.473+5000A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112890569 | ||||||
chr7:112890668 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+4901A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112890668 | ||||||
chr7:112890669 | A | T | 1 | a0001c0001t0003g0031 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.473+4900T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112890669 | ||||||
chr7:112890697 | T | C | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+4872A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112890697 | ||||||
chr7:112891029 | G | A | 13 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(10): Show | 15 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.473+4540C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112891029 | ||||||
chr7:112891102 | AT | A | 12 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(9): Show | 14 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.473+4466delA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112891102 | ||||||
chr7:112891199 | AATATTT | A | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+4364_473+4369d others(8): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112891199 | ||||||
chr7:112891284 | A | G | 1 | a0001c0001t0007g0012 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.473+4285T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112891284 | ||||||
chr7:112891394 | C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(190): Show | 200 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.473+4175G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112891394 | ||||||
chr7:112891596 | T | C | 1 | a0001c0001t0005g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.473+3973A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112891596 | ||||||
chr7:112891653 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.473+3916T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112891653 | ||||||
chr7:112892253 | G | GTTCCATT others(5): Show |
5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+3315_473+3316i others(14): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112892253 | ||||||
chr7:112892287 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.473+3282A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112892287 | ||||||
chr7:112892473 | A | C | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.473+3096T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112892473 | ||||||
chr7:112892583 | A | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(79): Show | 85 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.473+2986T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112892583 | ||||||
chr7:112892612 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.473+2957A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112892612 | ||||||
chr7:112892620 | A | C | 2 | a0001c0001t0002g0079a0001c0001t0002g0083 | 2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.473+2949T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112892620 | ||||||
chr7:112892771 | CA | C | 5 | a0001c0001t0001g0131a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG00735.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+2797delT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112892771 | ||||||
chr7:112892779 | A | T | 9 | a0001c0001t0004g0041a0001c0001t0004g0042a0001c0001t0004g0043others(6): Show | 9 | HG02280.hp2 HG02572.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.473+2790T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112892779 | ||||||
chr7:112892782 | A | T | 64 | a0001c0001t0001g0075a0001c0001t0001g0150a0001c0001t0001g0187others(61): Show | 65 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.473+2787T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112892782 | ||||||
chr7:112892882 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.473+2687G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112892882 | ||||||
chr7:112892965 | C | T | 2 | a0001c0001t0002g0099a0001c0001t0002g0121 | 2 | NA18970.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.473+2604G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112892965 | ||||||
chr7:112893000 | A | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG01433.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.473+2569T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112893000 | ||||||
chr7:112893234 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.473+2335C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112893234 | ||||||
chr7:112893237 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+2332C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112893237 | ||||||
chr7:112893377 | C | T | 6 | a0001c0001t0002g0096a0001c0001t0002g0099a0001c0001t0002g0100others(3): Show | 6 | HG00438.hp2 HG02027.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.473+2192G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112893377 | ||||||
chr7:112893727 | C | A | 1 | a0001c0001t0002g0094 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.473+1842G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112893727 | ||||||
chr7:112893954 | C | T | 1 | a0001c0001t0010g0105 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.473+1615G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112893954 | ||||||
chr7:112894453 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.473+1116G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112894453 | ||||||
chr7:112894569 | C | T | 1 | a0001c0001t0012g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.473+1000G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112894569 | ||||||
chr7:112894606 | G | C | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.473+963C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112894606 | ||||||
chr7:112894666 | T | C | 1 | a0001c0001t0002g0096 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.473+903A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112894666 | ||||||
chr7:112894697 | A | C | 1 | a0001c0001t0009g0091 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.473+872T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112894697 | ||||||
chr7:112895275 | A | C | 3 | a0001c0001t0006g0085a0001c0001t0006g0086a0001c0001t0006g0087 | 3 | HG02615.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.473+294T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 3/4 | chr7 | 112895275 | ||||||
chr7:112895869 | CTG | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-132_303-131del others(2): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112895869 | ||||||
chr7:112895901 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-162G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112895901 | ||||||
chr7:112896088 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-349A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112896088 | ||||||
chr7:112896158 | G | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-419C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112896158 | ||||||
chr7:112896191 | G | A | 6 | a0001c0001t0001g0075a0001c0001t0002g0065a0001c0001t0002g0066others(3): Show | 6 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-452C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112896191 | ||||||
chr7:112896195 | A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(189): Show | 199 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.303-456T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112896195 | ||||||
chr7:112896198 | C | T | 62 | a0001c0001t0001g0187a0001c0001t0002g0003a0001c0001t0002g0093others(59): Show | 63 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.303-459G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112896198 | ||||||
chr7:112896201 | G | C | 1 | a0001c0001t0001g0164 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.303-462C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112896201 | ||||||
chr7:112896205 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.303-466C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112896205 | ||||||
chr7:112896208 | CGTGT | C | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.303-473_303-470del others(4): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112896208 | ||||||
chr7:112896257 | A | G | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.303-518T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112896257 | ||||||
chr7:112896279 | TTTC | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-543_303-541del others(3): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112896279 | ||||||
chr7:112896281 | T | G | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-542A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112896281 | ||||||
chr7:112896282 | C | A | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-543G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112896282 | ||||||
chr7:112896546 | T | C | 1 | a0001c0001t0010g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.303-807A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112896546 | ||||||
chr7:112896576 | G | A | 1 | a0001c0001t0003g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.303-837C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112896576 | ||||||
chr7:112896685 | G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(73): Show | 79 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.303-946C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112896685 | ||||||
chr7:112897046 | G | A | 2 | a0001c0001t0002g0113a0001c0001t0002g0114 | 2 | HG00738.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.303-1307C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112897046 | ||||||
chr7:112897080 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-1341T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112897080 | ||||||
chr7:112897160 | G | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(79): Show | 85 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.303-1421C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112897160 | ||||||
chr7:112897294 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.303-1555G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112897294 | ||||||
chr7:112897444 | T | C | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.303-1705A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112897444 | ||||||
chr7:112897501 | C | T | 15 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.303-1762G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112897501 | ||||||
chr7:112897747 | G | C | 1 | a0001c0001t0005g0194 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.303-2008C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112897747 | ||||||
chr7:112897796 | C | T | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-2057G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112897796 | ||||||
chr7:112897921 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.303-2182A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112897921 | ||||||
chr7:112898021 | C | T | 1 | a0001c0001t0004g0044 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.303-2282G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112898021 | ||||||
chr7:112898037 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.303-2298T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112898037 | ||||||
chr7:112898323 | C | T | 44 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0094others(41): Show | 45 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.303-2584G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112898323 | ||||||
chr7:112898332 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-2593A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112898332 | ||||||
chr7:112898334 | G | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-2595C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112898334 | ||||||
chr7:112898466 | C | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(73): Show | 79 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.303-2727G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112898466 | ||||||
chr7:112898913 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-3174C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112898913 | ||||||
chr7:112899105 | A | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-3366T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112899105 | ||||||
chr7:112899490 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.303-3751G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112899490 | ||||||
chr7:112899639 | T | C | 1 | a0001c0001t0011g0073 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.303-3900A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112899639 | ||||||
chr7:112899655 | A | C | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.303-3916T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112899655 | ||||||
chr7:112899659 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-3920T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112899659 | ||||||
chr7:112899789 | G | GAAAAAAA others(2): Show |
73 | a0001c0001t0001g0075a0001c0001t0001g0186a0001c0001t0002g0003others(70): Show | 76 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.303-4059_303-4051d others(11): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112899789 | ||||||
chr7:112899789 | G | GAAAAAAA others(3): Show |
22 | a0001c0001t0001g0187a0001c0001t0002g0111a0001c0001t0002g0112others(19): Show | 22 | HG00673.hp2 HG00733.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.303-4060_303-4051d others(12): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112899789 | ||||||
chr7:112899789 | G | GAAAAAAA others(4): Show |
7 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0069others(4): Show | 8 | HG01192.hp2 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.303-4061_303-4051d others(13): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112899789 | ||||||
chr7:112899789 | G | GAAAAAAA others(5): Show |
1 | a0001c0002t0003g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.303-4062_303-4051d others(14): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112899789 | ||||||
chr7:112899789 | G | GAAAAAAA others(6): Show |
1 | a0001c0002t0008g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.303-4063_303-4051d others(15): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112899789 | ||||||
chr7:112899837 | C | T | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.303-4098G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112899837 | ||||||
chr7:112899991 | A | C | 1 | a0001c0001t0001g0123 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.303-4252T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112899991 | ||||||
chr7:112900098 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-4359C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112900098 | ||||||
chr7:112900105 | AT | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-4367delA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112900105 | ||||||
chr7:112900121 | CAT | C | 2 | a0001c0001t0001g0154a0001c0001t0002g0102 | 2 | HG01358.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.303-4384_303-4383d others(4): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112900121 | ||||||
chr7:112900135 | T | A | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-4396A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112900135 | ||||||
chr7:112900165 | A | T | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.303-4426T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112900165 | ||||||
chr7:112900294 | A | C | 117 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0186others(114): Show | 121 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(118): Show |
intron_variant | MODIFIER | c.303-4555T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112900294 | ||||||
chr7:112900597 | C | CAG | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-4860_303-4859d others(4): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112900597 | ||||||
chr7:112901125 | T | C | 1 | a0001c0001t0006g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.303-5386A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112901125 | ||||||
chr7:112901171 | G | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG01433.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.303-5432C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112901171 | ||||||
chr7:112901234 | G | A | 28 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0094others(25): Show | 29 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.303-5495C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112901234 | ||||||
chr7:112901259 | T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(189): Show | 199 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.303-5520A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112901259 | ||||||
chr7:112901347 | T | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.303-5608A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112901347 | ||||||
chr7:112901363 | A | C | 1 | a0001c0001t0003g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.303-5624T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112901363 | ||||||
chr7:112901371 | C | T | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG01891.hp2 HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.303-5632G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112901371 | ||||||
chr7:112901526 | C | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-5787G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112901526 | ||||||
chr7:112901566 | T | G | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.303-5827A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112901566 | ||||||
chr7:112901735 | TA | T | 6 | a0001c0001t0006g0059a0001c0001t0006g0060a0001c0001t0006g0061others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-5997delT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112901735 | ||||||
chr7:112901929 | C | T | 12 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(9): Show | 12 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.303-6190G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112901929 | ||||||
chr7:112902124 | C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0118a0001c0001t0001g0119others(35): Show | 40 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.303-6385G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902124 | ||||||
chr7:112902412 | G | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.303-6673C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902412 | ||||||
chr7:112902416 | C | CA | 17 | a0001c0001t0001g0120a0001c0001t0001g0128a0001c0001t0001g0129others(14): Show | 17 | HG00735.hp1 HG01358.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.303-6678dupT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902416 | ||||||
chr7:112902416 | C | CAA | 9 | a0001c0001t0001g0055a0001c0001t0001g0130a0001c0001t0001g0161others(6): Show | 9 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.303-6679_303-6678d others(4): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902416 | ||||||
chr7:112902416 | C | CAAAA | 10 | a0001c0001t0001g0004a0001c0001t0001g0076a0001c0001t0001g0118others(7): Show | 11 | HG00738.hp1 HG01106.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.303-6681_303-6678d others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902416 | ||||||
chr7:112902416 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0122 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303-6687_303-6678d others(12): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902416 | ||||||
chr7:112902416 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0126a0001c0001t0001g0131a0001c0001t0001g0137 | 3 | HG00673.hp1 HG01943.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.303-6688_303-6678d others(13): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902416 | ||||||
chr7:112902416 | C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0132a0001c0001t0001g0183 | 2 | HG01975.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.303-6678_303-6677i others(19): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902416 | ||||||
chr7:112902421 | AAAAAAAA others(11): Show |
A | 3 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0185 | 3 | HG00733.hp2 NA18951.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.303-6700_303-6683d others(20): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902421 | ||||||
chr7:112902422 | AAAAAAAC others(10): Show |
A | 2 | a0001c0001t0001g0056a0001c0001t0005g0193 | 2 | HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.303-6700_303-6684d others(19): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902422 | ||||||
chr7:112902424 | AAAAAC | A | 7 | a0001c0001t0005g0005a0001c0001t0005g0197a0001c0001t0005g0198others(4): Show | 8 | HG00099.hp1 HG01258.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.303-6690_303-6686d others(7): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902424 | ||||||
chr7:112902424 | AAAAACAA others(8): Show |
A | 1 | a0001c0001t0001g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.303-6700_303-6686d others(17): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902424 | ||||||
chr7:112902425 | A | C | 29 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0094others(26): Show | 30 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.303-6686T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902425 | ||||||
chr7:112902425 | AAAACAAA others(7): Show |
A | 2 | a0001c0001t0005g0006a0001c0001t0005g0192 | 3 | HG03490.hp2 HG03492.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.303-6700_303-6687d others(16): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902425 | ||||||
chr7:112902425 | AAAACAAA others(17): Show |
A | 3 | a0001c0002t0008g0034a0001c0002t0008g0036a0001c0002t0008g0037 | 3 | HG01192.hp2 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.303-6710_303-6687d others(26): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902425 | ||||||
chr7:112902426 | AAACAAAA others(6): Show |
A | 3 | a0001c0001t0005g0189a0001c0001t0006g0085a0001c0001t0006g0087 | 3 | HG02615.hp2 HG02717.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.303-6700_303-6688d others(15): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902426 | ||||||
chr7:112902426 | AAACAAAA others(16): Show |
A | 2 | a0001c0002t0003g0035a0001c0002t0008g0002 | 3 | HG02622.hp1 HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.303-6710_303-6688d others(25): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902426 | ||||||
chr7:112902427 | A | C | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.303-6688T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902427 | ||||||
chr7:112902427 | AACAAAAA others(5): Show |
A | 6 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0116others(3): Show | 6 | HG01346.hp1 HG01433.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-6700_303-6689d others(14): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902427 | ||||||
chr7:112902428 | AC | A | 4 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(1): Show | 4 | HG00099.hp2 HG01099.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.303-6690delG | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902428 | ||||||
chr7:112902429 | C | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(149): Show | 156 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.303-6690G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902429 | ||||||
chr7:112902431 | A | C | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.303-6692T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902431 | ||||||
chr7:112902433 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.303-6694T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902433 | ||||||
chr7:112902435 | A | C | 6 | a0001c0001t0001g0150a0001c0001t0001g0182a0001c0001t0003g0013others(3): Show | 6 | HG02040.hp1 HG02723.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-6696T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902435 | ||||||
chr7:112902437 | A | AC | 5 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0004g0048others(2): Show | 5 | HG02055.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-6699_303-6698i others(3): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902437 | ||||||
chr7:112902437 | A | C | 53 | a0001c0001t0001g0075a0001c0001t0001g0187a0001c0001t0002g0003others(50): Show | 54 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.303-6698T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902437 | ||||||
chr7:112902439 | C | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(152): Show | 160 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.303-6700G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902439 | ||||||
chr7:112902439 | C | CAA | 9 | a0001c0001t0003g0030a0001c0001t0004g0039a0001c0001t0004g0051others(6): Show | 9 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.303-6702_303-6701d others(4): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902439 | ||||||
chr7:112902448 | A | AAC | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-6710_303-6709i others(4): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902448 | ||||||
chr7:112902448 | A | C | 2 | a0001c0001t0006g0059a0001c0001t0006g0060 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.303-6709T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902448 | ||||||
chr7:112902449 | C | A | 69 | a0001c0001t0001g0004a0001c0001t0001g0055a0001c0001t0001g0056others(66): Show | 72 | HG00099.hp1 HG00673.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.303-6710G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902449 | ||||||
chr7:112902460 | A | C | 1 | a0001c0001t0003g0031 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.303-6721T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902460 | ||||||
chr7:112902462 | C | A | 22 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0004g0039others(19): Show | 22 | HG00673.hp2 HG01433.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.303-6723G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902462 | ||||||
chr7:112902568 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.303-6829G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902568 | ||||||
chr7:112902713 | G | C | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-6974C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112902713 | ||||||
chr7:112903026 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-7287G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112903026 | ||||||
chr7:112903042 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-7303T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112903042 | ||||||
chr7:112903090 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.303-7351C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112903090 | ||||||
chr7:112903142 | C | T | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.303-7403G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112903142 | ||||||
chr7:112903149 | T | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-7410A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112903149 | ||||||
chr7:112903237 | T | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-7498A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112903237 | ||||||
chr7:112903500 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-7761A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112903500 | ||||||
chr7:112903735 | T | C | 1 | a0001c0001t0009g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.303-7996A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112903735 | ||||||
chr7:112903870 | T | C | 14 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(11): Show | 16 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.303-8131A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112903870 | ||||||
chr7:112904529 | A | C | 1 | a0001c0001t0001g0160 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.303-8790T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112904529 | ||||||
chr7:112904547 | C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(188): Show | 198 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.303-8808G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112904547 | ||||||
chr7:112904575 | C | A | 1 | a0001c0001t0009g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.303-8836G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112904575 | ||||||
chr7:112904579 | CAAA | C | 28 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0094others(25): Show | 29 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.303-8843_303-8841d others(5): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112904579 | ||||||
chr7:112904618 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-8879C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112904618 | ||||||
chr7:112905041 | A | AT | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-9303dupA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112905041 | ||||||
chr7:112905145 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.303-9406C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112905145 | ||||||
chr7:112905149 | A | G | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-9410T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112905149 | ||||||
chr7:112905156 | C | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.303-9417G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112905156 | ||||||
chr7:112905217 | C | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-9478G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112905217 | ||||||
chr7:112905283 | T | G | 16 | a0001c0001t0004g0039a0001c0001t0004g0040a0001c0001t0004g0041others(13): Show | 16 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.303-9544A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112905283 | ||||||
chr7:112905783 | A | AAT | 15 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(12): Show | 16 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.302+9521_302+9522d others(4): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112905783 | ||||||
chr7:112905842 | T | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0168 | 2 | HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.302+9464A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112905842 | ||||||
chr7:112906255 | T | C | 7 | a0001c0001t0005g0005a0001c0001t0005g0194a0001c0001t0005g0195others(4): Show | 8 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.302+9051A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906255 | ||||||
chr7:112906420 | A | G | 11 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.302+8886T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906420 | ||||||
chr7:112906485 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+8821A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906485 | ||||||
chr7:112906523 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+8783A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906523 | ||||||
chr7:112906569 | A | AT | 9 | a0001c0001t0004g0041a0001c0001t0004g0042a0001c0001t0004g0043others(6): Show | 9 | HG02280.hp2 HG02572.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.302+8736dupA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906569 | ||||||
chr7:112906571 | A | T | 16 | a0001c0001t0004g0039a0001c0001t0004g0040a0001c0001t0004g0041others(13): Show | 16 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.302+8735T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906571 | ||||||
chr7:112906573 | C | CT | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(154): Show | 163 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.302+8732dupA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906573 | ||||||
chr7:112906573 | C | CTT | 6 | a0001c0001t0001g0075a0001c0001t0001g0169a0001c0001t0001g0170others(3): Show | 6 | HG01099.hp2 HG01123.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+8731_302+8732d others(4): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906573 | ||||||
chr7:112906573 | C | T | 16 | a0001c0001t0004g0039a0001c0001t0004g0040a0001c0001t0004g0041others(13): Show | 16 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.302+8733G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906573 | ||||||
chr7:112906587 | TG | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+8718delC | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906587 | ||||||
chr7:112906589 | A | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+8717T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906589 | ||||||
chr7:112906592 | C | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+8714G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906592 | ||||||
chr7:112906787 | G | T | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+8519C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906787 | ||||||
chr7:112906817 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+8489T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906817 | ||||||
chr7:112906848 | G | C | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG01891.hp2 HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.302+8458C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906848 | ||||||
chr7:112906873 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+8433C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906873 | ||||||
chr7:112906995 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.302+8311T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112906995 | ||||||
chr7:112907135 | G | A | 6 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+8171C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907135 | ||||||
chr7:112907319 | A | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0076a0001c0001t0001g0077others(31): Show | 35 | HG00673.hp1 HG00733.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.302+7987T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907319 | ||||||
chr7:112907394 | C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(190): Show | 200 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.302+7912G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907394 | ||||||
chr7:112907678 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+7628G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907678 | ||||||
chr7:112907831 | A | ATTCT | 7 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(4): Show | 7 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.302+7471_302+7474d others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907831 | ||||||
chr7:112907837 | A | T | 1 | a0001c0001t0003g0022 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.302+7469T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907837 | ||||||
chr7:112907838 | C | CTTAT | 3 | a0001c0001t0001g0058a0001c0001t0001g0123a0001c0001t0005g0194 | 3 | HG01361.hp2 HG01433.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.302+7467_302+7468i others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907838 | ||||||
chr7:112907838 | C | T | 1 | a0001c0001t0005g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.302+7468G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907838 | ||||||
chr7:112907842 | C | CTTACTTA others(5): Show |
2 | a0001c0001t0002g0003a0001c0001t0002g0093 | 3 | HG01123.hp1 HG02559.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.302+7463_302+7464i others(14): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907842 | ||||||
chr7:112907842 | C | CTTACTTA others(1): Show |
28 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0167others(25): Show | 28 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.302+7463_302+7464i others(10): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907842 | ||||||
chr7:112907842 | C | CTTACTTA others(5): Show |
4 | a0001c0001t0002g0098a0001c0001t0002g0117a0001c0001t0003g0024others(1): Show | 4 | HG00735.hp2 HG01243.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.302+7463_302+7464i others(14): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907842 | ||||||
chr7:112907842 | C | CTTACTTA others(9): Show |
3 | a0001c0001t0003g0025a0001c0001t0003g0029a0001c0001t0003g0033 | 3 | HG02717.hp1 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.302+7463_302+7464i others(18): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907842 | ||||||
chr7:112907842 | C | CTTAT | 96 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0074others(93): Show | 99 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.302+7460_302+7463d others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907842 | ||||||
chr7:112907842 | C | CTTATTTA others(1): Show |
18 | a0001c0001t0001g0076a0001c0001t0001g0125a0001c0001t0001g0127others(15): Show | 19 | HG01192.hp1 HG01192.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.302+7456_302+7463d others(10): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907842 | ||||||
chr7:112907842 | C | CTTATTTA others(5): Show |
4 | a0001c0001t0001g0187a0001c0001t0002g0069a0001c0001t0004g0040others(1): Show | 4 | HG02109.hp1 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.302+7452_302+7463d others(14): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907842 | ||||||
chr7:112907842 | C | T | 24 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(21): Show | 26 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.302+7464G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907842 | ||||||
chr7:112907842 | CTTATTTA others(1): Show |
C | 6 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+7456_302+7463d others(10): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907842 | ||||||
chr7:112907959 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.302+7347A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112907959 | ||||||
chr7:112908060 | G | A | 2 | a0001c0001t0002g0065a0001c0001t0002g0066 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.302+7246C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112908060 | ||||||
chr7:112908082 | T | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+7224A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112908082 | ||||||
chr7:112908516 | C | T | 4 | a0001c0002t0008g0002a0001c0002t0008g0034a0001c0002t0008g0036others(1): Show | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+6790G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112908516 | ||||||
chr7:112908722 | C | T | 6 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(3): Show | 6 | HG01168.hp1 HG02258.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+6584G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112908722 | ||||||
chr7:112908743 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+6563G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112908743 | ||||||
chr7:112908836 | C | G | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.302+6470G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112908836 | ||||||
chr7:112908858 | A | T | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+6448T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112908858 | ||||||
chr7:112908916 | C | G | 18 | a0001c0001t0001g0074a0001c0001t0005g0005a0001c0001t0005g0006others(15): Show | 20 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.302+6390G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112908916 | ||||||
chr7:112909297 | G | C | 13 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(10): Show | 15 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.302+6009C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112909297 | ||||||
chr7:112909619 | GTTATT | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+5682_302+5686d others(7): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112909619 | ||||||
chr7:112909699 | G | A | 44 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0094others(41): Show | 45 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.302+5607C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112909699 | ||||||
chr7:112909970 | T | G | 63 | a0001c0001t0001g0075a0001c0001t0001g0187a0001c0001t0002g0003others(60): Show | 64 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.302+5336A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112909970 | ||||||
chr7:112910048 | C | G | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.302+5258G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112910048 | ||||||
chr7:112910114 | C | T | 7 | a0001c0001t0005g0005a0001c0001t0005g0194a0001c0001t0005g0195others(4): Show | 8 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.302+5192G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112910114 | ||||||
chr7:112910156 | C | T | 13 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(10): Show | 15 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.302+5150G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112910156 | ||||||
chr7:112910157 | C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0168 | 2 | HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.302+5149G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112910157 | ||||||
chr7:112910319 | T | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG01433.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.302+4987A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112910319 | ||||||
chr7:112910323 | T | A | 1 | a0001c0001t0001g0176 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.302+4983A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112910323 | ||||||
chr7:112910613 | A | C | 1 | a0001c0001t0002g0067 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.302+4693T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112910613 | ||||||
chr7:112910707 | T | C | 33 | a0001c0001t0001g0074a0001c0001t0002g0079a0001c0001t0002g0080others(30): Show | 35 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.302+4599A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112910707 | ||||||
chr7:112911060 | G | C | 6 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(3): Show | 6 | HG01168.hp1 HG02258.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+4246C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112911060 | ||||||
chr7:112911428 | T | C | 18 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(15): Show | 18 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.302+3878A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112911428 | ||||||
chr7:112911480 | G | C | 71 | a0001c0001t0001g0075a0001c0001t0001g0186a0001c0001t0001g0187others(68): Show | 72 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.302+3826C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112911480 | ||||||
chr7:112911519 | A | G | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.302+3787T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112911519 | ||||||
chr7:112911532 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+3774A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112911532 | ||||||
chr7:112911639 | T | C | 1 | a0001c0001t0003g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.302+3667A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112911639 | ||||||
chr7:112911758 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.302+3548A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112911758 | ||||||
chr7:112911847 | C | G | 1 | a0001c0001t0012g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.302+3459G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112911847 | ||||||
chr7:112912037 | A | T | 16 | a0001c0001t0004g0039a0001c0001t0004g0040a0001c0001t0004g0041others(13): Show | 16 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.302+3269T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112912037 | ||||||
chr7:112912071 | C | CAGTA | 81 | a0001c0001t0001g0075a0001c0001t0001g0186a0001c0001t0001g0187others(78): Show | 83 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.302+3234_302+3235i others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112912071 | ||||||
chr7:112912119 | T | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG00099.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.302+3187A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112912119 | ||||||
chr7:112912234 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+3072G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112912234 | ||||||
chr7:112912302 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.302+3004G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112912302 | ||||||
chr7:112912392 | A | G | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+2914T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112912392 | ||||||
chr7:112912413 | TGTCA | T | 4 | a0001c0001t0003g0025a0001c0001t0003g0026a0001c0001t0003g0029others(1): Show | 4 | HG01243.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.302+2889_302+2892d others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112912413 | ||||||
chr7:112912461 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+2845A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112912461 | ||||||
chr7:112912756 | A | AT | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+2549dupA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112912756 | ||||||
chr7:112912782 | G | A | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.302+2524C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112912782 | ||||||
chr7:112912930 | T | C | 12 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(9): Show | 12 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.302+2376A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112912930 | ||||||
chr7:112912982 | G | A | 64 | a0001c0001t0001g0075a0001c0001t0001g0186a0001c0001t0001g0187others(61): Show | 65 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.302+2324C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112912982 | ||||||
chr7:112913105 | T | C | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+2201A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112913105 | ||||||
chr7:112913487 | TGCCCTTC others(5): Show |
T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+1807_302+1818d others(14): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112913487 | ||||||
chr7:112913773 | CTTGGTAG others(6): Show |
C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+1520_302+1532d others(15): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112913773 | ||||||
chr7:112913782 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.302+1524C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112913782 | ||||||
chr7:112913813 | T | C | 12 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(9): Show | 14 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.302+1493A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112913813 | ||||||
chr7:112913846 | C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0168 | 2 | HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.302+1460G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112913846 | ||||||
chr7:112913946 | G | A | 1 | a0001c0001t0003g0024 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.302+1360C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112913946 | ||||||
chr7:112914039 | A | G | 1 | a0001c0001t0012g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.302+1267T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914039 | ||||||
chr7:112914118 | T | A | 18 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(15): Show | 18 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.302+1188A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914118 | ||||||
chr7:112914129 | T | A | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.302+1177A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914129 | ||||||
chr7:112914275 | A | G | 71 | a0001c0001t0001g0075a0001c0001t0001g0186a0001c0001t0001g0187others(68): Show | 72 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.302+1031T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914275 | ||||||
chr7:112914276 | G | GT | 112 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(109): Show | 117 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.302+1029dupA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914276 | ||||||
chr7:112914276 | G | GTT | 9 | a0001c0001t0001g0057a0001c0001t0001g0075a0001c0001t0001g0139others(6): Show | 9 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.302+1028_302+1029d others(4): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914276 | ||||||
chr7:112914276 | G | GTTT | 25 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0002g0106others(22): Show | 26 | HG01167.hp2 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.302+1027_302+1029d others(5): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914276 | ||||||
chr7:112914276 | G | GTTTT | 41 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0094others(38): Show | 42 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.302+1026_302+1029d others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914276 | ||||||
chr7:112914276 | G | GTTTTT | 8 | a0001c0001t0002g0097a0001c0001t0004g0053a0001c0001t0007g0007others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.302+1025_302+1029d others(7): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914276 | ||||||
chr7:112914480 | T | C | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+826A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914480 | ||||||
chr7:112914488 | G | A | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.302+818C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914488 | ||||||
chr7:112914494 | T | A | 1 | a0001c0001t0001g0184 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.302+812A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914494 | ||||||
chr7:112914585 | C | T | 1 | a0001c0001t0006g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.302+721G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914585 | ||||||
chr7:112914686 | T | C | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+620A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914686 | ||||||
chr7:112914687 | A | G | 9 | a0001c0001t0004g0041a0001c0001t0004g0042a0001c0001t0004g0043others(6): Show | 9 | HG02280.hp2 HG02572.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.302+619T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914687 | ||||||
chr7:112914719 | C | G | 1 | a0001c0002t0003g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.302+587G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914719 | ||||||
chr7:112914743 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+563A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914743 | ||||||
chr7:112914762 | C | T | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+544G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914762 | ||||||
chr7:112914978 | C | T | 4 | a0001c0001t0001g0167a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG02723.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.302+328G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914978 | ||||||
chr7:112914979 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+327C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112914979 | ||||||
chr7:112915019 | T | A | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+287A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112915019 | ||||||
chr7:112915023 | G | C | 28 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0094others(25): Show | 29 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.302+283C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112915023 | ||||||
chr7:112915067 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.302+239G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112915067 | ||||||
chr7:112915162 | C | T | 1 | a0001c0001t0001g0184 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.302+144G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112915162 | ||||||
chr7:112915239 | G | GA | 9 | a0001c0001t0003g0013a0001c0001t0003g0015a0001c0001t0003g0016others(6): Show | 9 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.302+66dupT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 2/4 | chr7 | 112915239 | ||||||
chr7:112915548 | G | A | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.161-101C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112915548 | ||||||
chr7:112915674 | G | A | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-227C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112915674 | ||||||
chr7:112915892 | A | G | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0164others(1): Show | 4 | HG00438.hp1 HG02165.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-445T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112915892 | ||||||
chr7:112915926 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-479G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112915926 | ||||||
chr7:112916115 | T | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0127a0001c0001t0001g0128others(22): Show | 27 | HG00438.hp1 HG00735.hp1 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.161-668A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916115 | ||||||
chr7:112916252 | T | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(73): Show | 79 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.161-805A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916252 | ||||||
chr7:112916268 | T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(73): Show | 79 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.161-821A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916268 | ||||||
chr7:112916507 | G | A | 13 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(10): Show | 15 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-1060C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916507 | ||||||
chr7:112916535 | T | C | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-1088A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916535 | ||||||
chr7:112916590 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-1143A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916590 | ||||||
chr7:112916642 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-1195G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916642 | ||||||
chr7:112916652 | T | C | 6 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-1205A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916652 | ||||||
chr7:112916705 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-1258G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916705 | ||||||
chr7:112916706 | G | A | 4 | a0001c0001t0001g0135a0001c0001t0001g0151a0001c0001t0001g0158others(1): Show | 4 | HG02056.hp2 NA18951.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-1259C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916706 | ||||||
chr7:112916772 | C | T | 13 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(10): Show | 15 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-1325G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916772 | ||||||
chr7:112916773 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-1326C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916773 | ||||||
chr7:112916776 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.161-1329C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916776 | ||||||
chr7:112916800 | C | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-1353G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916800 | ||||||
chr7:112916807 | G | A | 28 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0094others(25): Show | 29 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.161-1360C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916807 | ||||||
chr7:112916853 | T | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-1406A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916853 | ||||||
chr7:112916874 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.161-1427C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916874 | ||||||
chr7:112916876 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.161-1429G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916876 | ||||||
chr7:112916943 | G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0159 | 2 | HG02148.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.161-1496C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112916943 | ||||||
chr7:112917126 | C | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-1679G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112917126 | ||||||
chr7:112917203 | C | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(73): Show | 79 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.161-1756G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112917203 | ||||||
chr7:112917285 | C | T | 6 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-1838G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112917285 | ||||||
chr7:112917441 | C | A | 1 | a0001c0001t0009g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-1994G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112917441 | ||||||
chr7:112917463 | C | A | 10 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(7): Show | 11 | HG01192.hp2 HG01975.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.161-2016G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112917463 | ||||||
chr7:112917516 | C | G | 2 | a0001c0001t0006g0085a0001c0001t0006g0086 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.161-2069G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112917516 | ||||||
chr7:112917538 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.161-2091G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112917538 | ||||||
chr7:112917611 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-2164T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112917611 | ||||||
chr7:112917715 | AT | A | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.161-2269delA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112917715 | ||||||
chr7:112917818 | T | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0168 | 2 | HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.161-2371A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112917818 | ||||||
chr7:112917916 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-2469A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112917916 | ||||||
chr7:112917957 | C | G | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG02818.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-2510G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112917957 | ||||||
chr7:112917965 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-2518A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112917965 | ||||||
chr7:112917981 | C | G | 1 | a0001c0001t0003g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.161-2534G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112917981 | ||||||
chr7:112918032 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.161-2585A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918032 | ||||||
chr7:112918097 | C | G | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-2650G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918097 | ||||||
chr7:112918118 | G | A | 4 | a0001c0002t0008g0002a0001c0002t0008g0034a0001c0002t0008g0036others(1): Show | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-2671C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918118 | ||||||
chr7:112918141 | G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(190): Show | 200 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.161-2694C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918141 | ||||||
chr7:112918242 | G | A | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-2795C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918242 | ||||||
chr7:112918281 | G | T | 7 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(4): Show | 7 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-2834C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918281 | ||||||
chr7:112918306 | G | C | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.161-2859C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918306 | ||||||
chr7:112918412 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-2965G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918412 | ||||||
chr7:112918415 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-2968A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918415 | ||||||
chr7:112918562 | A | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-3115T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918562 | ||||||
chr7:112918575 | G | A | 6 | a0001c0001t0012g0028a0001c0002t0003g0035a0001c0002t0008g0002others(3): Show | 7 | HG01192.hp2 HG02109.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-3128C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918575 | ||||||
chr7:112918601 | C | T | 10 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(7): Show | 11 | HG01192.hp2 HG01975.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.161-3154G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918601 | ||||||
chr7:112918617 | T | C | 2 | a0001c0001t0006g0085a0001c0001t0006g0086 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.161-3170A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918617 | ||||||
chr7:112918865 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.161-3418A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918865 | ||||||
chr7:112918899 | T | C | 2 | a0001c0001t0009g0089a0001c0001t0009g0090 | 2 | HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.161-3452A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918899 | ||||||
chr7:112918960 | G | A | 2 | a0001c0001t0011g0072a0001c0001t0011g0073 | 2 | NA19060.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.161-3513C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112918960 | ||||||
chr7:112919033 | G | T | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0136others(1): Show | 4 | HG00673.hp1 HG01192.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-3586C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112919033 | ||||||
chr7:112919039 | C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0160 | 2 | HG02647.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.161-3592G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112919039 | ||||||
chr7:112919180 | T | C | 13 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(10): Show | 15 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-3733A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112919180 | ||||||
chr7:112919192 | T | G | 5 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(2): Show | 5 | HG02630.hp2 HG02818.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-3745A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112919192 | ||||||
chr7:112919342 | A | G | 6 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-3895T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112919342 | ||||||
chr7:112919696 | C | T | 4 | a0001c0002t0008g0002a0001c0002t0008g0034a0001c0002t0008g0036others(1): Show | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-4249G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112919696 | ||||||
chr7:112919721 | A | G | 28 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0094others(25): Show | 29 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.161-4274T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112919721 | ||||||
chr7:112919772 | C | G | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.161-4325G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112919772 | ||||||
chr7:112919775 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.161-4328G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112919775 | ||||||
chr7:112919826 | C | T | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.161-4379G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112919826 | ||||||
chr7:112919868 | G | C | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-4421C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112919868 | ||||||
chr7:112919999 | C | T | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-4552G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112919999 | ||||||
chr7:112920004 | G | A | 29 | a0001c0001t0001g0185a0001c0001t0002g0003a0001c0001t0002g0093others(26): Show | 30 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.161-4557C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920004 | ||||||
chr7:112920065 | C | T | 6 | a0001c0001t0001g0186a0001c0002t0003g0035a0001c0002t0008g0002others(3): Show | 7 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-4618G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920065 | ||||||
chr7:112920127 | A | C | 2 | a0001c0001t0009g0070a0001c0001t0009g0091 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.161-4680T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920127 | ||||||
chr7:112920129 | T | A | 2 | a0001c0001t0009g0070a0001c0001t0009g0091 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.161-4682A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920129 | ||||||
chr7:112920229 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-4782A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920229 | ||||||
chr7:112920248 | G | A | 6 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(3): Show | 6 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-4801C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920248 | ||||||
chr7:112920340 | GA | G | 4 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(1): Show | 4 | HG02723.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-4894delT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920340 | ||||||
chr7:112920343 | A | C | 4 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(1): Show | 4 | HG02723.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-4896T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920343 | ||||||
chr7:112920348 | C | G | 4 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(1): Show | 4 | HG02723.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-4901G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920348 | ||||||
chr7:112920436 | G | A | 5 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(2): Show | 5 | HG02922.hp2 NA18947.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-4989C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920436 | ||||||
chr7:112920447 | T | C | 10 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(7): Show | 11 | HG01192.hp2 HG01975.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.161-5000A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920447 | ||||||
chr7:112920568 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-5121A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920568 | ||||||
chr7:112920667 | T | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-5220A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920667 | ||||||
chr7:112920702 | C | T | 1 | a0001c0001t0002g0096 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.161-5255G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920702 | ||||||
chr7:112920704 | C | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(175): Show | 184 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.161-5257G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920704 | ||||||
chr7:112920709 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-5262A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920709 | ||||||
chr7:112920715 | C | G | 1 | a0001c0001t0001g0055 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.161-5268G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920715 | ||||||
chr7:112920745 | C | A | 6 | a0001c0001t0001g0177a0001c0001t0002g0065a0001c0001t0002g0066others(3): Show | 6 | HG00099.hp2 HG01975.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-5298G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920745 | ||||||
chr7:112920746 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-5299C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920746 | ||||||
chr7:112920762 | C | T | 10 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(7): Show | 11 | HG01192.hp2 HG01975.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.161-5315G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920762 | ||||||
chr7:112920847 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-5400A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920847 | ||||||
chr7:112920850 | C | T | 4 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(1): Show | 4 | HG02723.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-5403G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920850 | ||||||
chr7:112920984 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.161-5537T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112920984 | ||||||
chr7:112921005 | A | G | 6 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(3): Show | 6 | HG01168.hp1 HG02258.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-5558T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921005 | ||||||
chr7:112921066 | T | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-5619A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921066 | ||||||
chr7:112921139 | G | T | 1 | a0001c0001t0002g0067 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.161-5692C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921139 | ||||||
chr7:112921177 | C | A | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-5730G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921177 | ||||||
chr7:112921177 | C | T | 18 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(15): Show | 18 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-5730G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921177 | ||||||
chr7:112921227 | T | C | 18 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(15): Show | 18 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-5780A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921227 | ||||||
chr7:112921328 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.161-5881G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921328 | ||||||
chr7:112921418 | C | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-5971G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921418 | ||||||
chr7:112921513 | T | A | 1 | a0001c0001t0004g0053 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.161-6066A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921513 | ||||||
chr7:112921560 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.161-6113G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921560 | ||||||
chr7:112921582 | C | A | 15 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-6135G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921582 | ||||||
chr7:112921686 | G | A | 3 | a0001c0001t0006g0085a0001c0001t0006g0086a0001c0001t0006g0087 | 3 | HG02615.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.161-6239C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921686 | ||||||
chr7:112921710 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.161-6263G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921710 | ||||||
chr7:112921775 | C | CAAGTGGG others(2): Show |
198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(195): Show | 205 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.161-6329_161-6328i others(11): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921775 | ||||||
chr7:112921909 | G | C | 1 | a0001c0001t0002g0115 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.161-6462C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921909 | ||||||
chr7:112921933 | G | T | 1 | a0001c0002t0003g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.161-6486C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921933 | ||||||
chr7:112921944 | CCCCTCT | C | 102 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0186others(99): Show | 105 | HG00099.hp1 HG00438.hp2 HG00673.hp2 others(102): Show |
intron_variant | MODIFIER | c.161-6503_161-6498d others(8): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921944 | ||||||
chr7:112921944 | CCCCTCTC others(5): Show |
C | 1 | a0001c0001t0003g0022 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.161-6509_161-6498d others(14): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921944 | ||||||
chr7:112921953 | C | A | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.161-6506G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921953 | ||||||
chr7:112921960 | TCTCCCTC others(5): Show |
T | 1 | a0001c0001t0003g0024 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.161-6525_161-6514d others(14): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921960 | ||||||
chr7:112921966 | T | G | 6 | a0001c0001t0002g0095a0001c0002t0003g0035a0001c0002t0008g0002others(3): Show | 7 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-6519A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921966 | ||||||
chr7:112921966 | T | TCTCCCG | 10 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 12 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.161-6525_161-6520d others(8): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921966 | ||||||
chr7:112921977 | C | T | 5 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(2): Show | 5 | HG01243.hp2 HG02717.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-6530G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112921977 | ||||||
chr7:112922079 | C | T | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-6632G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922079 | ||||||
chr7:112922101 | G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG01433.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.161-6654C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922101 | ||||||
chr7:112922105 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.161-6658C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922105 | ||||||
chr7:112922197 | A | C | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-6750T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922197 | ||||||
chr7:112922201 | G | A | 8 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0112others(5): Show | 8 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-6754C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922201 | ||||||
chr7:112922238 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.161-6791C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922238 | ||||||
chr7:112922289 | A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(190): Show | 200 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.161-6842T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922289 | ||||||
chr7:112922296 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-6849G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922296 | ||||||
chr7:112922349 | C | T | 15 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-6902G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922349 | ||||||
chr7:112922411 | C | T | 3 | a0001c0001t0001g0126a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG01943.hp2 HG01975.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.161-6964G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922411 | ||||||
chr7:112922420 | G | A | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-6973C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922420 | ||||||
chr7:112922565 | A | G | 10 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(7): Show | 11 | HG01192.hp2 HG01975.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.161-7118T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922565 | ||||||
chr7:112922568 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.161-7121G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922568 | ||||||
chr7:112922576 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-7129C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922576 | ||||||
chr7:112922644 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.161-7197G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922644 | ||||||
chr7:112922645 | A | G | 117 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0186others(114): Show | 121 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(118): Show |
intron_variant | MODIFIER | c.161-7198T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922645 | ||||||
chr7:112922684 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.161-7237G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922684 | ||||||
chr7:112922773 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-7326A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922773 | ||||||
chr7:112922799 | G | A | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.161-7352C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922799 | ||||||
chr7:112922819 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.161-7372G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922819 | ||||||
chr7:112922847 | GCCCGGCC others(43): Show |
G | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.161-7450_161-7401d others(52): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922847 | ||||||
chr7:112922859 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-7412T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922859 | ||||||
chr7:112922889 | GC | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0056others(125): Show | 132 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(129): Show |
intron_variant | MODIFIER | c.161-7443delG | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922889 | ||||||
chr7:112922891 | C | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-7444G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922891 | ||||||
chr7:112922895 | C | G | 6 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(3): Show | 6 | HG01168.hp1 HG02258.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-7448G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922895 | ||||||
chr7:112922897 | C | A | 2 | a0001c0001t0001g0162a0001c0001t0003g0023 | 2 | HG01496.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.161-7450G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922897 | ||||||
chr7:112922899 | C | A | 1 | a0001c0001t0003g0031 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.161-7452G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922899 | ||||||
chr7:112922901 | CG | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-7455delC | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922901 | ||||||
chr7:112922916 | A | G | 117 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0186others(114): Show | 121 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(118): Show |
intron_variant | MODIFIER | c.161-7469T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922916 | ||||||
chr7:112922921 | T | TGAGGGAG others(68): Show |
5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-7475_161-7474i others(77): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922921 | ||||||
chr7:112922952 | C | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-7505G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922952 | ||||||
chr7:112922991 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-7544G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112922991 | ||||||
chr7:112923191 | C | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-7744G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112923191 | ||||||
chr7:112923269 | C | A | 13 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(10): Show | 15 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-7822G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112923269 | ||||||
chr7:112923340 | C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(73): Show | 79 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.161-7893G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112923340 | ||||||
chr7:112923398 | C | G | 1 | a0001c0001t0005g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161-7951G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112923398 | ||||||
chr7:112923485 | T | A | 5 | a0001c0001t0005g0005a0001c0001t0005g0195a0001c0001t0005g0196others(2): Show | 6 | HG01099.hp1 HG01258.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-8038A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112923485 | ||||||
chr7:112923528 | T | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-8081A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112923528 | ||||||
chr7:112923577 | A | G | 1 | a0001c0001t0007g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.161-8130T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112923577 | ||||||
chr7:112923588 | A | G | 1 | a0001c0001t0007g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.161-8141T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112923588 | ||||||
chr7:112923679 | C | T | 5 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(2): Show | 5 | HG02922.hp2 NA18947.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-8232G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112923679 | ||||||
chr7:112923810 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-8363G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112923810 | ||||||
chr7:112924051 | C | G | 10 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(7): Show | 11 | HG01192.hp2 HG01975.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.161-8604G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112924051 | ||||||
chr7:112924051 | C | T | 1 | a0001c0001t0003g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.161-8604G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112924051 | ||||||
chr7:112924056 | G | A | 1 | a0001c0001t0005g0198 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-8609C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112924056 | ||||||
chr7:112924167 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-8720A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112924167 | ||||||
chr7:112924209 | A | G | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.161-8762T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112924209 | ||||||
chr7:112924277 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-8830C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112924277 | ||||||
chr7:112924416 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.161-8969G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112924416 | ||||||
chr7:112924585 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.161-9138C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112924585 | ||||||
chr7:112924680 | A | G | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.161-9233T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112924680 | ||||||
chr7:112924709 | T | C | 44 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0094others(41): Show | 45 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.161-9262A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112924709 | ||||||
chr7:112924718 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.161-9271A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112924718 | ||||||
chr7:112924734 | C | T | 5 | a0001c0001t0005g0006a0001c0001t0005g0189a0001c0001t0005g0190others(2): Show | 6 | HG03239.hp1 HG03490.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-9287G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112924734 | ||||||
chr7:112924819 | CT | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(166): Show | 175 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.161-9373delA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112924819 | ||||||
chr7:112924889 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.161-9442G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112924889 | ||||||
chr7:112925089 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-9642A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112925089 | ||||||
chr7:112925205 | A | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG01891.hp2 HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.161-9758T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112925205 | ||||||
chr7:112925362 | G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(190): Show | 200 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.161-9915C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112925362 | ||||||
chr7:112925484 | G | A | 8 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0112others(5): Show | 8 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-10037C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112925484 | ||||||
chr7:112925491 | C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(71): Show | 77 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.161-10044G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112925491 | ||||||
chr7:112925515 | T | C | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-10068A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112925515 | ||||||
chr7:112925596 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.161-10149G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112925596 | ||||||
chr7:112925599 | T | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-10152A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112925599 | ||||||
chr7:112925662 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-10215G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112925662 | ||||||
chr7:112925687 | G | A | 1 | a0001c0001t0003g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.161-10240C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112925687 | ||||||
chr7:112925794 | CA | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(180): Show | 189 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.161-10348delT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112925794 | ||||||
chr7:112925794 | CAA | C | 6 | a0001c0001t0001g0127a0001c0002t0003g0035a0001c0002t0008g0002others(3): Show | 7 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-10349_161-1034 others(6): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112925794 | ||||||
chr7:112925852 | T | C | 13 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0189others(10): Show | 15 | HG00099.hp1 HG01099.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-10405A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112925852 | ||||||
chr7:112926004 | G | C | 1 | a0001c0001t0002g0117 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.161-10557C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112926004 | ||||||
chr7:112926011 | C | T | 2 | a0001c0001t0001g0056a0001c0001t0002g0094 | 2 | HG03579.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.161-10564G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112926011 | ||||||
chr7:112926337 | C | G | 6 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(3): Show | 6 | HG01168.hp1 HG02258.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-10890G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112926337 | ||||||
chr7:112926612 | T | C | 1 | a0001c0002t0003g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.161-11165A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112926612 | ||||||
chr7:112926752 | T | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-11305A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112926752 | ||||||
chr7:112926821 | C | T | 1 | a0001c0002t0003g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.161-11374G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112926821 | ||||||
chr7:112927265 | AT | A | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.161-11819delA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112927265 | ||||||
chr7:112927288 | G | A | 28 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0094others(25): Show | 29 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.161-11841C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112927288 | ||||||
chr7:112927576 | T | G | 1 | a0001c0001t0001g0165 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.160+12015A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112927576 | ||||||
chr7:112927892 | C | T | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+11699G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112927892 | ||||||
chr7:112928311 | G | A | 1 | a0001c0001t0004g0039 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.160+11280C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112928311 | ||||||
chr7:112928421 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.160+11170C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112928421 | ||||||
chr7:112928421 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.160+11170C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112928421 | ||||||
chr7:112928444 | A | C | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+11147T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112928444 | ||||||
chr7:112928658 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.160+10933G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112928658 | ||||||
chr7:112928774 | A | AT | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.160+10816dupA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112928774 | ||||||
chr7:112928847 | T | G | 6 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+10744A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112928847 | ||||||
chr7:112928907 | C | T | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+10684G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112928907 | ||||||
chr7:112928977 | G | GA | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+10613dupT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112928977 | ||||||
chr7:112929108 | C | T | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+10483G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112929108 | ||||||
chr7:112929214 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+10377A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112929214 | ||||||
chr7:112929219 | A | T | 18 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(15): Show | 18 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.160+10372T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112929219 | ||||||
chr7:112929229 | T | TCATA | 28 | a0001c0001t0001g0187a0001c0001t0002g0065a0001c0001t0002g0066others(25): Show | 29 | HG01192.hp2 HG01243.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.160+10361_160+1036 others(8): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112929229 | ||||||
chr7:112929833 | C | T | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.160+9758G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112929833 | ||||||
chr7:112929959 | A | T | 1 | a0001c0001t0001g0124 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.160+9632T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112929959 | ||||||
chr7:112929989 | CA | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0076others(66): Show | 72 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.160+9601delT | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112929989 | ||||||
chr7:112930031 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.160+9560A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112930031 | ||||||
chr7:112930068 | G | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+9523C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112930068 | ||||||
chr7:112930221 | A | T | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+9370T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112930221 | ||||||
chr7:112930271 | C | T | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+9320G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112930271 | ||||||
chr7:112930360 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.160+9231G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112930360 | ||||||
chr7:112930447 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.160+9144T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112930447 | ||||||
chr7:112930642 | G | A | 1 | a0001c0001t0005g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.160+8949C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112930642 | ||||||
chr7:112930645 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+8946A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112930645 | ||||||
chr7:112930721 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.160+8870A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112930721 | ||||||
chr7:112930728 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.160+8863T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112930728 | ||||||
chr7:112930972 | G | A | 4 | a0001c0002t0008g0002a0001c0002t0008g0034a0001c0002t0008g0036others(1): Show | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+8619C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112930972 | ||||||
chr7:112930994 | C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG01192.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.160+8597G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112930994 | ||||||
chr7:112931177 | C | T | 28 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0094others(25): Show | 29 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.160+8414G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112931177 | ||||||
chr7:112931269 | G | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.160+8322C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112931269 | ||||||
chr7:112931287 | A | C | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.160+8304T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112931287 | ||||||
chr7:112931305 | CAA | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+8284_160+8285d others(4): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112931305 | ||||||
chr7:112931354 | ATC | A | 11 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.160+8235_160+8236d others(4): Show |
BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112931354 | ||||||
chr7:112931365 | C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(191): Show | 201 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.160+8226G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112931365 | ||||||
chr7:112931630 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.160+7961G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112931630 | ||||||
chr7:112931689 | G | A | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.160+7902C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112931689 | ||||||
chr7:112931804 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+7787C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112931804 | ||||||
chr7:112931810 | A | T | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.160+7781T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112931810 | ||||||
chr7:112932053 | G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG01346.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.160+7538C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112932053 | ||||||
chr7:112932228 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.160+7363A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112932228 | ||||||
chr7:112932495 | T | A | 1 | a0001c0001t0013g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.160+7096A>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112932495 | ||||||
chr7:112932731 | A | T | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0183 | 3 | NA19060.hp2 NA19066.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.160+6860T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112932731 | ||||||
chr7:112932732 | C | G | 2 | a0001c0001t0002g0003a0001c0001t0002g0093 | 3 | HG01123.hp1 HG02559.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.160+6859G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112932732 | ||||||
chr7:112933141 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+6450C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112933141 | ||||||
chr7:112933209 | T | C | 1 | a0001c0001t0002g0121 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.160+6382A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112933209 | ||||||
chr7:112933270 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+6321A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112933270 | ||||||
chr7:112933331 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.160+6260C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112933331 | ||||||
chr7:112933423 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+6168T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112933423 | ||||||
chr7:112933424 | G | A | 1 | a0001c0001t0001g0184 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.160+6167C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112933424 | ||||||
chr7:112933494 | T | G | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+6097A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112933494 | ||||||
chr7:112933588 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+6003A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112933588 | ||||||
chr7:112933779 | A | C | 1 | a0001c0001t0003g0024 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.160+5812T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112933779 | ||||||
chr7:112933995 | A | G | 2 | a0001c0001t0002g0065a0001c0001t0002g0066 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.160+5596T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112933995 | ||||||
chr7:112934178 | T | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0076others(67): Show | 74 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.160+5413A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112934178 | ||||||
chr7:112934579 | A | G | 4 | a0001c0002t0008g0002a0001c0002t0008g0034a0001c0002t0008g0036others(1): Show | 5 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+5012T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112934579 | ||||||
chr7:112934725 | A | T | 1 | a0001c0002t0003g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.160+4866T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112934725 | ||||||
chr7:112934749 | T | G | 18 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(15): Show | 18 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.160+4842A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112934749 | ||||||
chr7:112934871 | A | G | 1 | a0001c0002t0008g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.160+4720T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112934871 | ||||||
chr7:112934882 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+4709A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112934882 | ||||||
chr7:112934933 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.160+4658G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112934933 | ||||||
chr7:112935094 | A | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(190): Show | 200 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.160+4497T>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112935094 | ||||||
chr7:112935267 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.160+4324C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112935267 | ||||||
chr7:112935586 | CT | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(190): Show | 200 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.160+4004delA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112935586 | ||||||
chr7:112935686 | T | C | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+3905A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112935686 | ||||||
chr7:112935766 | C | G | 1 | a0001c0001t0009g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.160+3825G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112935766 | ||||||
chr7:112935807 | T | C | 10 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(7): Show | 10 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+3784A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112935807 | ||||||
chr7:112935811 | C | A | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.160+3780G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112935811 | ||||||
chr7:112935893 | A | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+3698T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112935893 | ||||||
chr7:112936323 | G | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+3268C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112936323 | ||||||
chr7:112936415 | A | G | 23 | a0001c0001t0001g0187a0001c0001t0003g0017a0001c0001t0003g0018others(20): Show | 24 | HG01192.hp2 HG01243.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.160+3176T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112936415 | ||||||
chr7:112936567 | A | T | 6 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+3024T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112936567 | ||||||
chr7:112936978 | A | G | 1 | a0001c0001t0004g0039 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.160+2613T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112936978 | ||||||
chr7:112937050 | C | T | 15 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.160+2541G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112937050 | ||||||
chr7:112937164 | G | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.160+2427C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112937164 | ||||||
chr7:112937336 | T | C | 1 | a0001c0001t0003g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.160+2255A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112937336 | ||||||
chr7:112937338 | T | C | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+2253A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112937338 | ||||||
chr7:112937338 | T | G | 1 | a0001c0001t0003g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.160+2253A>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112937338 | ||||||
chr7:112937458 | G | C | 10 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(7): Show | 10 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+2133C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112937458 | ||||||
chr7:112937549 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.160+2042A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112937549 | ||||||
chr7:112937697 | A | G | 2 | a0001c0001t0002g0065a0001c0001t0002g0066 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.160+1894T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112937697 | ||||||
chr7:112937810 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.160+1781C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112937810 | ||||||
chr7:112937900 | T | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+1691A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112937900 | ||||||
chr7:112937992 | G | C | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+1599C>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112937992 | ||||||
chr7:112938108 | C | T | 7 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(4): Show | 7 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+1483G>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112938108 | ||||||
chr7:112938332 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.160+1259A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112938332 | ||||||
chr7:112938375 | G | T | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.160+1216C>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112938375 | ||||||
chr7:112938620 | A | G | 10 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(7): Show | 10 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+971T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112938620 | ||||||
chr7:112938677 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.160+914T>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112938677 | ||||||
chr7:112938705 | T | C | 4 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(1): Show | 4 | HG02723.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+886A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112938705 | ||||||
chr7:112938947 | T | C | 28 | a0001c0001t0001g0187a0001c0001t0002g0065a0001c0001t0002g0066others(25): Show | 29 | HG01192.hp2 HG01243.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.160+644A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112938947 | ||||||
chr7:112938948 | C | G | 4 | a0001c0001t0001g0074a0001c0001t0011g0071a0001c0001t0011g0072others(1): Show | 4 | NA18947.hp2 NA18950.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+643G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112938948 | ||||||
chr7:112938962 | GT | G | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+628delA | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112938962 | ||||||
chr7:112939080 | T | C | 28 | a0001c0001t0001g0187a0001c0001t0002g0065a0001c0001t0002g0066others(25): Show | 29 | HG01192.hp2 HG01243.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.160+511A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112939080 | ||||||
chr7:112939154 | C | A | 1 | a0001c0001t0002g0188 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.160+437G>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112939154 | ||||||
chr7:112939196 | T | C | 37 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(34): Show | 38 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.160+395A>G | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112939196 | ||||||
chr7:112939200 | C | G | 1 | a0001c0001t0009g0070 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160+391G>C | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112939200 | ||||||
chr7:112939274 | G | A | 5 | a0001c0002t0003g0035a0001c0002t0008g0002a0001c0002t0008g0034others(2): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+317C>T | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112939274 | ||||||
chr7:112939300 | A | T | 47 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(44): Show | 48 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.160+291T>A | BMT2 | ENSG00000164603.12 | transcript | ENST00000297145.9 | protein_coding | 1/4 | chr7 | 112939300 |