geneid | 84057 |
---|---|
ensemblid | ENSG00000121211.8 |
hgncid | 24839 |
symbol | MND1 |
name | meiotic nuclear divisions 1 |
refseq_nuc | NM_032117.4 |
refseq_prot | NP_115493.1 |
ensembl_nuc | ENST00000240488.8 |
ensembl_prot | ENSP00000240488.3 |
mane_status | MANE Select |
chr | chr4 |
start | 153344688 |
end | 153415118 |
strand | + |
ver | v1.2 |
region | chr4:153344688-153415118 |
region5000 | chr4:153339688-153420118 |
regionname0 | MND1_chr4_153344688_153415118 |
regionname5000 | MND1_chr4_153339688_153420118 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 205 | 337 | 98 | 54 | 132 | 14 | 37 | 101 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
a0002 | 0/0 | 205 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
a0003 | 0/0 | 205 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 618 | 314 | 87 | 49 | 130 | 14 | 32 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
c0002 | 0/0 | 618 | 19 | 7 | 5 | 2 | 0 | 5 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
c0003 | 0/0 | 618 | 4 | 4 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
c0004 | 0/0 | 618 | 4 | 0 | 0 | 4 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
c0005 | 0/0 | 618 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 312 | 208 | 58 | 37 | 78 | 9 | 24 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
t0002 | 0/0 | 312 | 109 | 29 | 12 | 55 | 5 | 8 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
t0003 | 0/0 | 309 | 20 | 7 | 5 | 2 | 0 | 6 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
t0004 | 0/0 | 289 | 4 | 4 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
t0005 | 0/0 | 312 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 618 | 314 | 87 | 49 | 130 | 14 | 32 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
a0001c0002 | 0/0 | 618 | 19 | 7 | 5 | 2 | 0 | 5 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
a0001c0003 | 0/0 | 618 | 4 | 4 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
a0002c0004 | 0/0 | 618 | 4 | 0 | 0 | 4 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
a0003c0005 | 0/0 | 618 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 929 | 207 | 57 | 37 | 78 | 9 | 24 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
a0001c0001t0002 | 0/0 | 929 | 104 | 29 | 12 | 51 | 5 | 7 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
a0001c0001t0003 | 0/0 | 926 | 2 | 1 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
a0001c0001t0005 | 0/0 | 929 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
a0001c0002t0001 | 0/0 | 929 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
a0001c0002t0003 | 0/0 | 926 | 18 | 6 | 5 | 2 | 0 | 5 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
a0001c0003t0004 | 0/0 | 906 | 4 | 4 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
a0002c0004t0002 | 0/0 | 929 | 4 | 0 | 0 | 4 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
a0003c0005t0002 | 0/0 | 929 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | copy fasta | chr4 | 153339688 | 153420118 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0002t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0003t0004g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0003t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0001c0003t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0002c0004t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0002c0004t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0002c0004t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0002c0004t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
a0003c0005t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | GBR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | GBR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0317 | EUR | FIN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | FIN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00408 | hp2 | a0002 | c0004 | t0002 | g0290 | EAS | CHS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | CHS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01070 | hp1 | a0001 | c0002 | t0003 | g0122 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01071 | hp2 | a0001 | c0002 | t0003 | g0123 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01081 | hp1 | a0001 | c0002 | t0003 | g0121 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01243 | hp1 | a0001 | c0002 | t0003 | g0013 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01261 | hp2 | a0001 | c0002 | t0003 | g0116 | AMR | CLM | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | CLM | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | CLM | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0300 | EUR | IBS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0296 | EUR | IBS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0301 | EUR | IBS | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01884 | hp2 | a0001 | c0002 | t0003 | g0127 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01891 | hp1 | a0001 | c0002 | t0003 | g0131 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | PEL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02083 | hp2 | a0001 | c0002 | t0003 | g0119 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0332 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0320 | AMR | PEL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0327 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PEL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02572 | hp2 | a0001 | c0002 | t0003 | g0011 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02735 | hp1 | a0001 | c0002 | t0003 | g0117 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0321 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0331 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02896 | hp2 | a0001 | c0003 | t0004 | g0004 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02897 | hp1 | a0001 | c0003 | t0004 | g0004 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0311 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02970 | hp2 | a0001 | c0003 | t0004 | g0099 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | MSL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03139 | hp1 | a0001 | c0002 | t0003 | g0012 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0335 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | MSL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0328 | AFR | MSL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | MSL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03491 | hp2 | a0001 | c0002 | t0003 | g0124 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03492 | hp2 | a0001 | c0002 | t0003 | g0125 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0333 | AFR | MSL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03654 | hp2 | a0003 | c0005 | t0002 | g0254 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | STU | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0304 | SAS | STU | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0048 | SAS | BEB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0277 | SAS | BEB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03834 | hp1 | a0001 | c0002 | t0003 | g0120 | SAS | BEB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0318 | SAS | BEB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | STU | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | STU | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG04228 | hp2 | a0001 | c0002 | t0003 | g0090 | SAS | STU | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18522 | hp1 | a0001 | c0003 | t0004 | g0100 | AFR | YRI | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | CHB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18954 | hp1 | a0001 | c0002 | t0003 | g0118 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18987 | hp2 | a0002 | c0004 | t0002 | g0292 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18998 | hp1 | a0002 | c0004 | t0002 | g0273 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18998 | hp2 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19002 | hp2 | a0002 | c0004 | t0002 | g0291 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | LWK | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | LWK | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0336 | AFR | ASW | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ASW | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0256 | EUR | TSI | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | TSI | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | GIH | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | GIH | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0330 | AFR | ACB | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03471 | hp1 | a0001 | c0002 | t0003 | g0128 | AFR | MSL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG06807 | hp1 | a0001 | c0002 | t0003 | g0130 | AFR | USA | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | USA | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | USA | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | USA | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | LWK | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0161 | REF | REF | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0142 | REF | REF | MND1_chr4_153339688_153420118 | MND1 | chr4 | 153339688 | 153420118 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:153350117
|
A | G | 1 | a0003 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.57A>G | p.Ile19Met | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/8 | 107/929 | 57/618 | 19/205 | chr4 | 153350117 | ||
chr4:153358600
|
A | T | 1 | a0002 | 4 | HG00408.hp2 NA18987.hp2 NA18998.hp1 others(1): Show |
missense_variant | MODERATE | c.254A>T | p.Lys85Met | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/8 | 304/929 | 254/618 | 85/205 | chr4 | 153358600 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:153355704
|
A | G | 1 | a0001c0002 | 19 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
synonymous_variant | LOW | c.120A>G | p.Lys40Lys | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/8 | 170/929 | 120/618 | 40/205 | chr4 | 153355704 | ||
chr4:153414812
|
T | C | 1 | a0001c0003 | 4 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(1): Show |
synonymous_variant | LOW | c.573T>C | p.Ile191Ile | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 8/8 | 623/929 | 573/618 | 191/205 | chr4 | 153414812 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:153414953
|
CTG | C | 3 | a0001c0001t0003a0001c0002t0003a0001c0003t0004 | 24 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*100_*101delGT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 8/8 | 100 | INFO_REALIGN_3_PRIME | chr4 | 153414953 | ||||
chr4:153415022
|
A | T | 6 | a0001c0001t0002a0001c0001t0003a0001c0002t0003others(3): Show | 133 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*165A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 8/8 | 165 | chr4 | 153415022 | |||||
chr4:153415041
|
C | T | 1 | a0001c0001t0005 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*184C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 8/8 | 184 | chr4 | 153415041 | |||||
chr4:153415114
|
AT | A | 3 | a0001c0001t0003a0001c0002t0003a0001c0003t0004 | 24 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*250delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 8/8 | 250 | INFO_REALIGN_3_PRIME | chr4 | 153415114 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:153344964
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(81): Show | 87 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.3+224G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153344964 | ||||||
chr4:153345131
|
T | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009 | 3 | HG01070.hp2 HG01993.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.3+391T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153345131 | ||||||
chr4:153345162
|
G | GC | 81 | a0001c0001t0001g0319a0001c0001t0001g0325a0001c0001t0002g0005others(78): Show | 83 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.3+430dupC | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 153345162 | |||||
chr4:153345167
|
C | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(82): Show | 88 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.3+427C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153345167 | ||||||
chr4:153345420
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3+680T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153345420 | ||||||
chr4:153345454
|
G | A | 1 | a0001c0002t0003g0090 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3+714G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153345454 | ||||||
chr4:153345594
|
CA | C | 11 | a0001c0001t0002g0326a0001c0001t0002g0327a0001c0001t0002g0328others(8): Show | 11 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3+855delA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153345594 | ||||||
chr4:153345601
|
C | T | 17 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0243others(14): Show | 17 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(14): Show |
intron_variant | MODIFIER | c.3+861C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153345601 | ||||||
chr4:153345821
|
G | A | 123 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(120): Show | 126 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.3+1081G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153345821 | ||||||
chr4:153345958
|
AATCT | A | 80 | a0001c0001t0001g0319a0001c0001t0002g0005a0001c0001t0002g0006others(77): Show | 82 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.3+1223_3+1226delAT others(2): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 153345958 | |||||
chr4:153346113
|
G | A | 11 | a0001c0002t0003g0090a0001c0002t0003g0116a0001c0002t0003g0117others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.3+1373G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153346113 | ||||||
chr4:153346353
|
C | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.3+1613C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153346353 | ||||||
chr4:153346641
|
A | C | 4 | a0001c0001t0002g0321a0001c0001t0002g0322a0001c0001t0002g0323others(1): Show | 4 | HG01891.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+1901A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153346641 | ||||||
chr4:153346669
|
G | T | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3+1929G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153346669 | ||||||
chr4:153346672
|
A | G | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3+1932A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153346672 | ||||||
chr4:153346783
|
G | C | 1 | a0001c0001t0001g0126 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3+2043G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153346783 | ||||||
chr4:153346824
|
A | G | 9 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(6): Show | 9 | HG02055.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3+2084A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153346824 | ||||||
chr4:153346838
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3+2098A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153346838 | ||||||
chr4:153346927
|
T | C | 132 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(129): Show | 134 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.3+2187T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153346927 | ||||||
chr4:153346975
|
T | C | 9 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(6): Show | 9 | HG02055.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3+2235T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153346975 | ||||||
chr4:153347018
|
A | T | 139 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(136): Show | 142 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.3+2278A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153347018 | ||||||
chr4:153347040
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3+2300G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153347040 | ||||||
chr4:153347158
|
A | G | 1 | a0001c0001t0002g0320 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3+2418A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153347158 | ||||||
chr4:153347356
|
C | T | 87 | a0001c0001t0001g0132a0001c0001t0001g0319a0001c0001t0002g0005others(84): Show | 89 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.3+2616C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153347356 | ||||||
chr4:153347389
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3+2649G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153347389 | ||||||
chr4:153347412
|
T | C | 9 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(6): Show | 9 | HG02055.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.4-2652T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153347412 | ||||||
chr4:153347475
|
G | A | 17 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0243others(14): Show | 17 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(14): Show |
intron_variant | MODIFIER | c.4-2589G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153347475 | ||||||
chr4:153347708
|
C | A | 3 | a0001c0003t0004g0004a0001c0003t0004g0099a0001c0003t0004g0100 | 4 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-2356C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153347708 | ||||||
chr4:153347779
|
A | C | 1 | a0001c0002t0003g0090 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4-2285A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153347779 | ||||||
chr4:153347821
|
C | T | 2 | a0001c0001t0002g0091a0001c0001t0002g0092 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4-2243C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153347821 | ||||||
chr4:153347963
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4-2101G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153347963 | ||||||
chr4:153348247
|
A | G | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4-1817A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153348247 | ||||||
chr4:153348289
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.4-1775G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153348289 | ||||||
chr4:153348296
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4-1768A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153348296 | ||||||
chr4:153348350
|
C | T | 86 | a0001c0001t0001g0319a0001c0001t0002g0005a0001c0001t0002g0006others(83): Show | 88 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.4-1714C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153348350 | ||||||
chr4:153348559
|
A | G | 86 | a0001c0001t0001g0319a0001c0001t0002g0005a0001c0001t0002g0006others(83): Show | 88 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.4-1505A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153348559 | ||||||
chr4:153348663
|
T | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(124): Show | 131 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.4-1401T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153348663 | ||||||
chr4:153348726
|
G | C | 86 | a0001c0001t0001g0319a0001c0001t0002g0005a0001c0001t0002g0006others(83): Show | 88 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.4-1338G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153348726 | ||||||
chr4:153348800
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4-1264C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153348800 | ||||||
chr4:153349002
|
A | T | 1 | a0001c0001t0001g0103 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4-1062A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153349002 | ||||||
chr4:153349012
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.4-1052A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153349012 | ||||||
chr4:153349094
|
CT | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 128 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.4-954delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 153349094 | |||||
chr4:153349094
|
CTT | C | 100 | a0001c0001t0001g0319a0001c0001t0002g0005a0001c0001t0002g0006others(97): Show | 102 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.4-955_4-954delTT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 153349094 | |||||
chr4:153349198
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02132.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.4-866A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153349198 | ||||||
chr4:153349298
|
A | G | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4-766A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153349298 | ||||||
chr4:153349317
|
C | A | 1 | a0001c0002t0003g0116 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4-747C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153349317 | ||||||
chr4:153349328
|
C | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.4-736C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153349328 | ||||||
chr4:153349363
|
A | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(38): Show | 43 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.4-701A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153349363 | ||||||
chr4:153349429
|
T | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(88): Show | 94 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.4-635T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153349429 | ||||||
chr4:153349467
|
C | A | 1 | a0001c0001t0001g0015 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4-597C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153349467 | ||||||
chr4:153349528
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.4-536G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153349528 | ||||||
chr4:153349562
|
G | T | 17 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0243others(14): Show | 17 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(14): Show |
intron_variant | MODIFIER | c.4-502G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153349562 | ||||||
chr4:153349651
|
C | G | 1 | a0001c0002t0003g0131 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4-413C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153349651 | ||||||
chr4:153349652
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4-412C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153349652 | ||||||
chr4:153349703
|
TTTATGTA | T | 17 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0243others(14): Show | 17 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(14): Show |
intron_variant | MODIFIER | c.4-360_4-354delTTAT others(3): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153349703 | ||||||
chr4:153349876
|
C | T | 3 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG02280.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4-188C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153349876 | ||||||
chr4:153350046
|
T | G | 1 | a0001c0001t0001g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4-18T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 1/7 | chr4 | 153350046 | ||||||
chr4:153350172
|
A | G | 19 | a0001c0002t0001g0129a0001c0002t0003g0011a0001c0002t0003g0012others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.69+43A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153350172 | ||||||
chr4:153350571
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(73): Show | 78 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.69+442G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153350571 | ||||||
chr4:153350750
|
A | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.69+621A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153350750 | ||||||
chr4:153350855
|
T | C | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+726T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153350855 | ||||||
chr4:153350860
|
A | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(92): Show | 97 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.69+731A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153350860 | ||||||
chr4:153350949
|
A | G | 19 | a0001c0002t0001g0129a0001c0002t0003g0011a0001c0002t0003g0012others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.69+820A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153350949 | ||||||
chr4:153350951
|
T | TA | 87 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(84): Show | 89 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.69+840dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153350951 | |||||
chr4:153350951
|
T | TAAAA | 11 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 12 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.69+837_69+840dupAA others(2): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153350951 | |||||
chr4:153350951
|
TA | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(100): Show | 105 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.69+840delA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153350951 | |||||
chr4:153350964
|
A | C | 4 | a0001c0002t0003g0122a0001c0002t0003g0123a0001c0002t0003g0124others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+835A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153350964 | ||||||
chr4:153350974
|
C | A | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107 | 3 | HG02055.hp2 HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.69+845C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153350974 | ||||||
chr4:153351033
|
A | G | 19 | a0001c0002t0001g0129a0001c0002t0003g0011a0001c0002t0003g0012others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.69+904A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153351033 | ||||||
chr4:153351109
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.69+980T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153351109 | ||||||
chr4:153351128
|
T | A | 1 | a0001c0001t0001g0137 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.69+999T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153351128 | ||||||
chr4:153351268
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.69+1139A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153351268 | ||||||
chr4:153351275
|
A | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(39): Show | 44 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.69+1146A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153351275 | ||||||
chr4:153351593
|
G | T | 2 | a0001c0002t0003g0130a0001c0002t0003g0131 | 2 | HG01891.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.69+1464G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153351593 | ||||||
chr4:153351638
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.69+1509G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153351638 | ||||||
chr4:153352040
|
T | TA | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(73): Show | 78 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.69+1916dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153352040 | |||||
chr4:153352442
|
A | G | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG02109.hp1 HG02886.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+2313A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153352442 | ||||||
chr4:153352683
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 111 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.69+2554G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153352683 | ||||||
chr4:153352740
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.69+2611C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153352740 | ||||||
chr4:153352746
|
T | TA | 77 | a0001c0001t0001g0319a0001c0001t0002g0005a0001c0001t0002g0006others(74): Show | 79 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.69+2639dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153352746 | |||||
chr4:153352746
|
TA | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(140): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.69+2639delA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153352746 | |||||
chr4:153352746
|
TAA | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(58): Show | 63 | HG00099.hp1 HG00140.hp1 HG01074.hp2 others(60): Show |
intron_variant | MODIFIER | c.69+2638_69+2639del others(2): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153352746 | |||||
chr4:153352746
|
TAAA | T | 23 | a0001c0001t0001g0009a0001c0001t0001g0089a0001c0001t0001g0101others(20): Show | 23 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.69+2637_69+2639del others(3): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153352746 | |||||
chr4:153353026
|
A | G | 1 | a0001c0001t0002g0309 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.70-2628A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153353026 | ||||||
chr4:153353053
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.70-2601G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153353053 | ||||||
chr4:153353218
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.70-2436C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153353218 | ||||||
chr4:153353396
|
C | T | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-2258C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153353396 | ||||||
chr4:153353404
|
C | CAT | 41 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0141others(38): Show | 42 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.70-2207_70-2206dup others(2): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353404
|
C | CATAT | 33 | a0001c0001t0001g0132a0001c0001t0001g0138a0001c0001t0001g0139others(30): Show | 33 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.70-2209_70-2206dup others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353404
|
C | CATATAT | 14 | a0001c0001t0001g0134a0001c0001t0001g0149a0001c0001t0001g0150others(11): Show | 14 | HG01496.hp1 HG01934.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.70-2211_70-2206dup others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353404
|
C | CATATATA others(1): Show |
5 | a0001c0001t0001g0103a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG01255.hp2 HG01975.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-2213_70-2206dup others(8): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353404
|
C | CATATATA others(3): Show |
5 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-2215_70-2206dup others(10): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353404
|
CAT | C | 29 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0133others(26): Show | 29 | HG00597.hp2 HG01106.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.70-2207_70-2206del others(2): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353404
|
CATAT | C | 28 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(25): Show | 28 | HG00642.hp2 HG01256.hp1 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.70-2209_70-2206del others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353404
|
CATATAT | C | 22 | a0001c0001t0001g0101a0001c0001t0001g0111a0001c0001t0002g0256others(19): Show | 22 | HG00408.hp2 HG01496.hp2 HG02717.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-2211_70-2206del others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353404
|
CATATATA others(1): Show |
C | 17 | a0001c0001t0001g0018a0001c0001t0001g0093a0001c0001t0001g0094others(14): Show | 18 | HG00642.hp1 HG01516.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.70-2213_70-2206del others(8): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353404
|
CATATATA others(3): Show |
C | 21 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0020others(18): Show | 22 | HG00323.hp1 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-2215_70-2206del others(10): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353404
|
CATATATA others(5): Show |
C | 20 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0025others(17): Show | 20 | HG00558.hp2 HG00735.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.70-2217_70-2206del others(12): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353404
|
CATATATA others(7): Show |
C | 22 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0036others(19): Show | 23 | HG00408.hp1 HG01516.hp2 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.70-2219_70-2206del others(14): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353404
|
CATATATA others(9): Show |
C | 9 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0049others(6): Show | 10 | HG01081.hp2 HG02615.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-2221_70-2206del others(16): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353404
|
CATATATA others(11): Show |
C | 10 | a0001c0001t0001g0053a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 10 | HG00099.hp1 HG00140.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-2223_70-2206del others(18): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353404
|
CATATATA others(13): Show |
C | 11 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 12 | HG01070.hp2 HG01074.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.70-2225_70-2206del others(20): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353404
|
CATATATA others(15): Show |
C | 15 | a0001c0001t0001g0055a0001c0001t0001g0067a0001c0001t0001g0068others(12): Show | 15 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.70-2227_70-2206del others(22): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153353404 | |||||
chr4:153353512
|
C | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.70-2142C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153353512 | ||||||
chr4:153353553
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.70-2101G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153353553 | ||||||
chr4:153353760
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.70-1894C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153353760 | ||||||
chr4:153353823
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.70-1831G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153353823 | ||||||
chr4:153353843
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(114): Show | 121 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.70-1811T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153353843 | ||||||
chr4:153353935
|
G | T | 1 | a0001c0001t0002g0005 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.70-1719G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153353935 | ||||||
chr4:153353967
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.70-1687G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153353967 | ||||||
chr4:153354144
|
G | GT | 88 | a0001c0001t0001g0156a0001c0001t0001g0217a0001c0001t0001g0319others(85): Show | 90 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.70-1500dupT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153354144 | |||||
chr4:153354183
|
G | A | 110 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(107): Show | 112 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.70-1471G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153354183 | ||||||
chr4:153354211
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.70-1443C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153354211 | ||||||
chr4:153354226
|
C | T | 1 | a0001c0001t0002g0293 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.70-1428C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153354226 | ||||||
chr4:153354322
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.70-1332A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153354322 | ||||||
chr4:153354542
|
G | T | 1 | a0001c0001t0003g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.70-1112G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153354542 | ||||||
chr4:153354627
|
C | T | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-1027C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153354627 | ||||||
chr4:153354648
|
A | G | 2 | a0001c0001t0002g0274a0001c0001t0002g0281 | 2 | NA18980.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.70-1006A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153354648 | ||||||
chr4:153354739
|
T | G | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.70-915T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153354739 | ||||||
chr4:153354934
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.70-720G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153354934 | ||||||
chr4:153354984
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-670G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153354984 | ||||||
chr4:153355023
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.70-631G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153355023 | ||||||
chr4:153355163
|
CA | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.70-481delA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 153355163 | |||||
chr4:153355184
|
A | G | 3 | a0001c0003t0004g0004a0001c0003t0004g0099a0001c0003t0004g0100 | 4 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-470A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153355184 | ||||||
chr4:153355374
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-280G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153355374 | ||||||
chr4:153355453
|
A | C | 1 | a0001c0001t0002g0309 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.70-201A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153355453 | ||||||
chr4:153355542
|
C | T | 18 | a0001c0002t0001g0129a0001c0002t0003g0011a0001c0002t0003g0012others(15): Show | 18 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.70-112C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153355542 | ||||||
chr4:153355619
|
C | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(38): Show | 43 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.70-35C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153355619 | ||||||
chr4:153355620
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-34G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 2/7 | chr4 | 153355620 | ||||||
chr4:153356029
|
C | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.127+318C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356029 | ||||||
chr4:153356051
|
A | T | 1 | a0001c0002t0001g0129 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.127+340A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356051 | ||||||
chr4:153356062
|
C | T | 17 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0243others(14): Show | 17 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(14): Show |
intron_variant | MODIFIER | c.127+351C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356062 | ||||||
chr4:153356064
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.127+353C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356064 | ||||||
chr4:153356095
|
C | T | 80 | a0001c0001t0001g0319a0001c0001t0002g0005a0001c0001t0002g0006others(77): Show | 82 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.127+384C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356095 | ||||||
chr4:153356171
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 138 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.127+460G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356171 | ||||||
chr4:153356220
|
TG | T | 5 | a0001c0001t0002g0253a0001c0001t0002g0255a0001c0001t0002g0256others(2): Show | 5 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+510delG | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356220 | ||||||
chr4:153356283
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(114): Show | 121 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.127+572T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356283 | ||||||
chr4:153356357
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0080 | 3 | HG01074.hp2 HG01106.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.127+646C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356357 | ||||||
chr4:153356361
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.127+650C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356361 | ||||||
chr4:153356377
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.127+666C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356377 | ||||||
chr4:153356410
|
G | A | 1 | a0001c0002t0003g0090 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.127+699G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356410 | ||||||
chr4:153356552
|
C | CA | 187 | a0001c0001t0001g0054a0001c0001t0001g0081a0001c0001t0001g0101others(184): Show | 189 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.127+865dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 153356552 | |||||
chr4:153356552
|
C | CAA | 57 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(54): Show | 59 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.127+864_127+865dup others(2): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 153356552 | |||||
chr4:153356552
|
C | CAAA | 39 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 40 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.127+863_127+865dup others(3): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 153356552 | |||||
chr4:153356552
|
C | CAAAA | 6 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0017others(3): Show | 7 | HG01516.hp2 HG01517.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+862_127+865dup others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 153356552 | |||||
chr4:153356552
|
CAA | C | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+864_127+865del others(2): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 153356552 | |||||
chr4:153356552
|
CAAAAAAA others(2): Show |
C | 8 | a0001c0001t0002g0326a0001c0001t0002g0327a0001c0001t0002g0329others(5): Show | 8 | HG02055.hp1 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.127+857_127+865del others(9): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 153356552 | |||||
chr4:153356660
|
T | A | 86 | a0001c0001t0001g0319a0001c0001t0002g0005a0001c0001t0002g0006others(83): Show | 88 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.127+949T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356660 | ||||||
chr4:153356763
|
A | G | 1 | a0001c0002t0003g0131 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127+1052A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356763 | ||||||
chr4:153356790
|
A | T | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.127+1079A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356790 | ||||||
chr4:153356802
|
A | G | 2 | a0001c0002t0003g0116a0001c0002t0003g0121 | 2 | HG01081.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.127+1091A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153356802 | ||||||
chr4:153357071
|
C | T | 1 | a0001c0001t0002g0265 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.127+1360C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153357071 | ||||||
chr4:153357349
|
G | A | 1 | a0001c0001t0002g0005 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.128-1125G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153357349 | ||||||
chr4:153357403
|
A | G | 19 | a0001c0002t0001g0129a0001c0002t0003g0011a0001c0002t0003g0012others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-1071A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153357403 | ||||||
chr4:153357433
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(88): Show | 94 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.128-1041C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153357433 | ||||||
chr4:153357551
|
AG | A | 17 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0243others(14): Show | 17 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(14): Show |
intron_variant | MODIFIER | c.128-921delG | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 153357551 | |||||
chr4:153357580
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.128-894C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153357580 | ||||||
chr4:153357921
|
A | G | 7 | a0001c0001t0001g0088a0001c0001t0001g0093a0001c0001t0001g0094others(4): Show | 7 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-553A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153357921 | ||||||
chr4:153357999
|
C | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-475C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153357999 | ||||||
chr4:153358093
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 138 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.128-381T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153358093 | ||||||
chr4:153358097
|
A | G | 8 | a0001c0001t0001g0144a0001c0001t0001g0154a0001c0001t0001g0155others(5): Show | 8 | HG00558.hp1 HG01496.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.128-377A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153358097 | ||||||
chr4:153358101
|
A | C | 1 | a0001c0002t0003g0131 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.128-373A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153358101 | ||||||
chr4:153358110
|
A | T | 1 | a0001c0002t0003g0117 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.128-364A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153358110 | ||||||
chr4:153358226
|
A | G | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-248A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153358226 | ||||||
chr4:153358291
|
A | T | 1 | a0001c0001t0002g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.128-183A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153358291 | ||||||
chr4:153358296
|
T | A | 17 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0243others(14): Show | 17 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(14): Show |
intron_variant | MODIFIER | c.128-178T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153358296 | ||||||
chr4:153358335
|
A | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-139A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153358335 | ||||||
chr4:153358471
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02109.hp1 NA18522.hp2 |
splice_region_variant&intron_variant | LOW | c.128-3T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 3/7 | chr4 | 153358471 | ||||||
chr4:153358744
|
A | C | 1 | a0001c0001t0002g0298 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.276+122A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153358744 | ||||||
chr4:153358792
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.276+170C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153358792 | ||||||
chr4:153358875
|
A | G | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.276+253A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153358875 | ||||||
chr4:153358983
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.276+361C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153358983 | ||||||
chr4:153359060
|
G | A | 17 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0243others(14): Show | 17 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(14): Show |
intron_variant | MODIFIER | c.276+438G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153359060 | ||||||
chr4:153359272
|
T | C | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.276+650T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153359272 | ||||||
chr4:153359554
|
T | A | 1 | a0001c0001t0002g0295 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.276+932T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153359554 | ||||||
chr4:153359580
|
A | C | 7 | a0001c0001t0001g0171a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.276+958A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153359580 | ||||||
chr4:153359600
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.276+978T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153359600 | ||||||
chr4:153359664
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0217 | 2 | HG02056.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.276+1042C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153359664 | ||||||
chr4:153359711
|
TA | T | 5 | a0001c0001t0002g0253a0001c0001t0002g0255a0001c0001t0002g0256others(2): Show | 5 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+1090delA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153359711 | ||||||
chr4:153359779
|
CT | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(287): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.276+1180delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153359779 | |||||
chr4:153359779
|
CTT | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0066a0001c0001t0001g0080others(3): Show | 6 | HG01256.hp2 HG01515.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.276+1179_276+1180d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153359779 | |||||
chr4:153359809
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0216 | 2 | HG00140.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.276+1187C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153359809 | ||||||
chr4:153359810
|
G | A | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0104 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.276+1188G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153359810 | ||||||
chr4:153359851
|
G | A | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.276+1229G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153359851 | ||||||
chr4:153359979
|
G | A | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(2): Show | 5 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+1357G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153359979 | ||||||
chr4:153359995
|
C | A | 1 | a0001c0001t0001g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.276+1373C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153359995 | ||||||
chr4:153360271
|
A | T | 1 | a0001c0001t0001g0190 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.276+1649A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153360271 | ||||||
chr4:153360305
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.276+1683G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153360305 | ||||||
chr4:153360405
|
A | G | 9 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(6): Show | 9 | HG02055.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.276+1783A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153360405 | ||||||
chr4:153360530
|
T | C | 5 | a0001c0001t0002g0253a0001c0001t0002g0255a0001c0001t0002g0256others(2): Show | 5 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+1908T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153360530 | ||||||
chr4:153360584
|
A | ATG | 4 | a0001c0001t0001g0143a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | NA18963.hp2 NA18991.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+1984_276+1985d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153360584 | |||||
chr4:153360584
|
A | G | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.276+1962A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153360584 | ||||||
chr4:153360584
|
ATG | A | 154 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(151): Show | 156 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.276+1984_276+1985d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153360584 | |||||
chr4:153360584
|
ATGTGTG | A | 5 | a0001c0001t0001g0141a0001c0001t0001g0174a0001c0001t0001g0175others(2): Show | 5 | HG02622.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.276+1980_276+1985d others(8): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153360584 | |||||
chr4:153360602
|
G | GTA | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009 | 3 | HG01070.hp2 HG01993.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.276+1981_276+1982i others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153360602 | |||||
chr4:153360602
|
G | GTATA | 6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.276+1981_276+1982i others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153360602 | |||||
chr4:153360604
|
G | A | 24 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(21): Show | 25 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.276+1982G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153360604 | ||||||
chr4:153360606
|
G | A | 183 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(180): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.276+1984G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153360606 | ||||||
chr4:153360606
|
G | GTA | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(40): Show | 46 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.276+1995_276+1996d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153360606 | |||||
chr4:153360608
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.276+1986A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153360608 | ||||||
chr4:153360617
|
T | C | 2 | a0001c0002t0003g0127a0001c0002t0003g0128 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.276+1995T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153360617 | ||||||
chr4:153360667
|
T | TATAA | 104 | a0001c0001t0001g0126a0001c0001t0001g0132a0001c0001t0001g0134others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.276+2065_276+2068d others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153360667 | |||||
chr4:153360675
|
A | AATAT | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 214 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.276+2056_276+2057i others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153360675 | |||||
chr4:153360709
|
G | C | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.276+2087G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153360709 | ||||||
chr4:153360770
|
CATATACA others(3): Show |
C | 113 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(110): Show | 115 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.276+2163_276+2172d others(12): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153360770 | |||||
chr4:153360803
|
A | C | 2 | a0001c0001t0002g0091a0001c0001t0002g0092 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.276+2181A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153360803 | ||||||
chr4:153360885
|
T | G | 138 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(135): Show | 141 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.276+2263T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153360885 | ||||||
chr4:153361145
|
A | G | 1 | a0001c0001t0002g0241 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.276+2523A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153361145 | ||||||
chr4:153361274
|
T | G | 1 | a0001c0001t0001g0319 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.276+2652T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153361274 | ||||||
chr4:153361403
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.276+2781C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153361403 | ||||||
chr4:153361566
|
G | A | 1 | a0001c0002t0003g0131 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.276+2944G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153361566 | ||||||
chr4:153361575
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.276+2953C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153361575 | ||||||
chr4:153361694
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.276+3072C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153361694 | ||||||
chr4:153361727
|
A | C | 2 | a0001c0002t0003g0122a0001c0002t0003g0123 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.276+3105A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153361727 | ||||||
chr4:153361827
|
G | C | 17 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0243others(14): Show | 17 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(14): Show |
intron_variant | MODIFIER | c.276+3205G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153361827 | ||||||
chr4:153361841
|
GAA | G | 98 | a0001c0001t0001g0319a0001c0001t0002g0005a0001c0001t0002g0006others(95): Show | 100 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.276+3228_276+3229d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153361841 | |||||
chr4:153361899
|
G | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 14 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.276+3277G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153361899 | ||||||
chr4:153361984
|
T | C | 4 | a0001c0001t0001g0143a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | NA18963.hp2 NA18991.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+3362T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153361984 | ||||||
chr4:153362163
|
A | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0297a0001c0001t0002g0316 | 3 | NA18951.hp1 NA18960.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.276+3541A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153362163 | ||||||
chr4:153362229
|
T | G | 7 | a0001c0001t0001g0088a0001c0001t0001g0093a0001c0001t0001g0094others(4): Show | 7 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.276+3607T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153362229 | ||||||
chr4:153362341
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.276+3719T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153362341 | ||||||
chr4:153362394
|
G | A | 1 | a0001c0002t0003g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.276+3772G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153362394 | ||||||
chr4:153362416
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.276+3794G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153362416 | ||||||
chr4:153362426
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.276+3804C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153362426 | ||||||
chr4:153362513
|
T | C | 16 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(13): Show | 17 | HG01255.hp2 HG02257.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.276+3891T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153362513 | ||||||
chr4:153362588
|
T | G | 1 | a0001c0001t0002g0263 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.276+3966T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153362588 | ||||||
chr4:153362668
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.276+4046G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153362668 | ||||||
chr4:153362842
|
T | TA | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG02109.hp1 HG02886.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.276+4221dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153362842 | |||||
chr4:153363098
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.276+4476C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153363098 | ||||||
chr4:153363139
|
T | C | 19 | a0001c0002t0001g0129a0001c0002t0003g0011a0001c0002t0003g0012others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.276+4517T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153363139 | ||||||
chr4:153363214
|
CT | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 229 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.276+4606delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153363214 | |||||
chr4:153363356
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.276+4734C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153363356 | ||||||
chr4:153363361
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.276+4739G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153363361 | ||||||
chr4:153363434
|
A | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 104 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.276+4812A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153363434 | ||||||
chr4:153363439
|
C | T | 3 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG02280.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.276+4817C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153363439 | ||||||
chr4:153363504
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(222): Show | 231 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.276+4882A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153363504 | ||||||
chr4:153363596
|
A | T | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.276+4974A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153363596 | ||||||
chr4:153363766
|
A | G | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.276+5144A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153363766 | ||||||
chr4:153363783
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.276+5161A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153363783 | ||||||
chr4:153363976
|
G | T | 1 | a0001c0002t0003g0120 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.276+5354G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153363976 | ||||||
chr4:153364041
|
C | G | 2 | a0001c0002t0003g0127a0001c0002t0003g0128 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.276+5419C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153364041 | ||||||
chr4:153364083
|
A | T | 11 | a0001c0001t0001g0137a0001c0001t0001g0148a0001c0001t0001g0156others(8): Show | 11 | HG00609.hp1 HG00621.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.276+5461A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153364083 | ||||||
chr4:153364098
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.276+5476G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153364098 | ||||||
chr4:153364137
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 149 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.276+5515T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153364137 | ||||||
chr4:153364352
|
C | CA | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.276+5737dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153364352 | |||||
chr4:153364361
|
G | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 114 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.276+5739G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153364361 | ||||||
chr4:153364401
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.276+5779C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153364401 | ||||||
chr4:153364468
|
A | G | 4 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(1): Show | 4 | HG02280.hp1 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+5846A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153364468 | ||||||
chr4:153364490
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.276+5868T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153364490 | ||||||
chr4:153364518
|
G | GA | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(96): Show | 103 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.276+5910dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153364518 | |||||
chr4:153364518
|
G | GAA | 6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0002g0258others(3): Show | 6 | HG02280.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.276+5909_276+5910d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153364518 | |||||
chr4:153364534
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.276+5912C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153364534 | ||||||
chr4:153364650
|
A | G | 4 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(1): Show | 4 | HG02280.hp1 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+6028A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153364650 | ||||||
chr4:153364692
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(96): Show | 102 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.276+6070C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153364692 | ||||||
chr4:153364706
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 131 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.276+6084G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153364706 | ||||||
chr4:153364887
|
G | A | 1 | a0001c0002t0003g0131 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.276+6265G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153364887 | ||||||
chr4:153364889
|
A | G | 79 | a0001c0001t0001g0319a0001c0001t0002g0005a0001c0001t0002g0006others(76): Show | 81 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.276+6267A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153364889 | ||||||
chr4:153365083
|
ACCAGATG others(6): Show |
A | 1 | a0001c0001t0001g0226 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.276+6465_276+6477d others(15): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153365083 | |||||
chr4:153365101
|
C | CA | 29 | a0001c0001t0001g0144a0001c0001t0001g0149a0001c0001t0001g0154others(26): Show | 29 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.276+6495dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153365101 | |||||
chr4:153365101
|
CA | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 203 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.276+6495delA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153365101 | |||||
chr4:153365221
|
T | C | 17 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(14): Show | 17 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.276+6599T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153365221 | ||||||
chr4:153365242
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.276+6620G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153365242 | ||||||
chr4:153365380
|
T | G | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.276+6758T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153365380 | ||||||
chr4:153365519
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.276+6897A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153365519 | ||||||
chr4:153365651
|
G | C | 19 | a0001c0002t0001g0129a0001c0002t0003g0011a0001c0002t0003g0012others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.276+7029G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153365651 | ||||||
chr4:153365758
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.276+7136C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153365758 | ||||||
chr4:153365960
|
A | G | 79 | a0001c0001t0001g0319a0001c0001t0002g0005a0001c0001t0002g0006others(76): Show | 81 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.276+7338A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153365960 | ||||||
chr4:153365969
|
T | TTC | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.276+7350_276+7351d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153365969 | |||||
chr4:153366010
|
C | A | 4 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(1): Show | 4 | HG02280.hp1 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+7388C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153366010 | ||||||
chr4:153366091
|
C | A | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.276+7469C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153366091 | ||||||
chr4:153366135
|
A | G | 1 | a0001c0001t0002g0264 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.276+7513A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153366135 | ||||||
chr4:153366144
|
T | C | 10 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.276+7522T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153366144 | ||||||
chr4:153366176
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.276+7554G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153366176 | ||||||
chr4:153366178
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.276+7556G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153366178 | ||||||
chr4:153366265
|
C | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0080 | 3 | HG01074.hp2 HG01106.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.276+7643C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153366265 | ||||||
chr4:153366326
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.276+7704G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153366326 | ||||||
chr4:153366347
|
C | T | 10 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.276+7725C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153366347 | ||||||
chr4:153366396
|
A | G | 1 | a0001c0001t0002g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.276+7774A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153366396 | ||||||
chr4:153366461
|
C | T | 1 | a0001c0002t0003g0119 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.276+7839C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153366461 | ||||||
chr4:153366615
|
C | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.276+7993C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153366615 | ||||||
chr4:153366642
|
A | G | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.276+8020A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153366642 | ||||||
chr4:153366974
|
G | A | 81 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0002g0005others(78): Show | 83 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.276+8352G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153366974 | ||||||
chr4:153367011
|
C | G | 85 | a0001c0001t0001g0046a0001c0001t0001g0084a0001c0001t0001g0141others(82): Show | 87 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.276+8389C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153367011 | ||||||
chr4:153367307
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.276+8685C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153367307 | ||||||
chr4:153367750
|
T | C | 14 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(11): Show | 14 | HG02145.hp2 HG02257.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.276+9128T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153367750 | ||||||
chr4:153368105
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.276+9483T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153368105 | ||||||
chr4:153368197
|
T | C | 1 | a0001c0001t0002g0299 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.276+9575T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153368197 | ||||||
chr4:153368362
|
G | T | 1 | a0001c0001t0001g0319 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.276+9740G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153368362 | ||||||
chr4:153368371
|
C | T | 10 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.276+9749C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153368371 | ||||||
chr4:153368482
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.276+9860A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153368482 | ||||||
chr4:153368664
|
G | C | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.276+10042G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153368664 | ||||||
chr4:153368809
|
T | TA | 11 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0300others(8): Show | 13 | HG00323.hp1 HG00741.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.276+10196dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153368809 | |||||
chr4:153368817
|
A | C | 1 | a0001c0001t0001g0210 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.276+10195A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153368817 | ||||||
chr4:153369103
|
T | C | 11 | a0001c0001t0001g0088a0001c0001t0001g0093a0001c0001t0001g0094others(8): Show | 11 | HG01255.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.276+10481T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153369103 | ||||||
chr4:153369431
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.276+10809C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153369431 | ||||||
chr4:153369550
|
T | A | 12 | a0001c0001t0003g0048a0001c0002t0003g0090a0001c0002t0003g0116others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.276+10928T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153369550 | ||||||
chr4:153369565
|
A | G | 33 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0115others(30): Show | 35 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.276+10943A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153369565 | ||||||
chr4:153369577
|
ATACTT | A | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.276+10958_276+1096 others(9): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153369577 | |||||
chr4:153369718
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.276+11096C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153369718 | ||||||
chr4:153370071
|
T | C | 11 | a0001c0001t0001g0088a0001c0001t0001g0093a0001c0001t0001g0094others(8): Show | 11 | HG01255.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.276+11449T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153370071 | ||||||
chr4:153370098
|
A | G | 11 | a0001c0001t0001g0137a0001c0001t0001g0148a0001c0001t0001g0156others(8): Show | 11 | HG00609.hp1 HG00621.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.276+11476A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153370098 | ||||||
chr4:153370100
|
C | T | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.276+11478C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153370100 | ||||||
chr4:153370102
|
T | C | 2 | a0001c0002t0003g0122a0001c0002t0003g0123 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.276+11480T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153370102 | ||||||
chr4:153370139
|
G | A | 6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.276+11517G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153370139 | ||||||
chr4:153370142
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.276+11520C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153370142 | ||||||
chr4:153370209
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.276+11587G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153370209 | ||||||
chr4:153370214
|
G | A | 22 | a0001c0001t0001g0025a0001c0001t0003g0048a0001c0002t0003g0011others(19): Show | 23 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.276+11592G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153370214 | ||||||
chr4:153370484
|
G | A | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(2): Show | 5 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+11862G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153370484 | ||||||
chr4:153370614
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.276+11992G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153370614 | ||||||
chr4:153370987
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.276+12365A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153370987 | ||||||
chr4:153371058
|
A | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0181 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.276+12436A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153371058 | ||||||
chr4:153371073
|
A | ATTGCC | 3 | a0001c0001t0001g0153a0001c0001t0001g0159a0001c0001t0001g0325 | 3 | HG02738.hp1 HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.276+12454_276+1245 others(9): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153371073 | |||||
chr4:153371164
|
G | A | 105 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(102): Show | 107 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.276+12542G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153371164 | ||||||
chr4:153371252
|
A | T | 1 | a0001c0002t0003g0131 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.276+12630A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153371252 | ||||||
chr4:153371387
|
C | G | 1 | a0001c0002t0003g0117 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.276+12765C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153371387 | ||||||
chr4:153371506
|
T | C | 1 | a0001c0001t0002g0328 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.276+12884T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153371506 | ||||||
chr4:153371671
|
G | A | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(2): Show | 5 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+13049G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153371671 | ||||||
chr4:153371770
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.276+13148C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153371770 | ||||||
chr4:153371775
|
A | C | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.276+13153A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153371775 | ||||||
chr4:153371837
|
G | C | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.276+13215G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153371837 | ||||||
chr4:153371964
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.276+13342A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153371964 | ||||||
chr4:153372011
|
G | T | 4 | a0001c0001t0002g0321a0001c0001t0002g0322a0001c0001t0002g0323others(1): Show | 4 | HG01891.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+13389G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153372011 | ||||||
chr4:153372054
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.276+13432C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153372054 | ||||||
chr4:153372321
|
A | ACC | 9 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(6): Show | 9 | HG02055.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.276+13700_276+1370 others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153372321 | |||||
chr4:153372373
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.276+13751A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153372373 | ||||||
chr4:153372387
|
A | T | 81 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(78): Show | 83 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.276+13765A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153372387 | ||||||
chr4:153373056
|
T | G | 1 | a0001c0001t0001g0016 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.276+14434T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153373056 | ||||||
chr4:153373068
|
A | G | 1 | a0001c0001t0002g0295 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.276+14446A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153373068 | ||||||
chr4:153373540
|
A | T | 2 | a0001c0002t0003g0124a0001c0002t0003g0125 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.276+14918A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153373540 | ||||||
chr4:153373604
|
T | C | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.276+14982T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153373604 | ||||||
chr4:153373904
|
A | G | 2 | a0001c0001t0002g0294a0001c0001t0002g0311 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.276+15282A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153373904 | ||||||
chr4:153373906
|
T | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0235 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.276+15284T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153373906 | ||||||
chr4:153373964
|
A | C | 11 | a0001c0001t0001g0088a0001c0001t0001g0093a0001c0001t0001g0094others(8): Show | 11 | HG01255.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.276+15342A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153373964 | ||||||
chr4:153373989
|
G | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0009 | 2 | HG01070.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.276+15367G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153373989 | ||||||
chr4:153374267
|
G | A | 2 | a0001c0002t0003g0127a0001c0002t0003g0128 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.276+15645G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153374267 | ||||||
chr4:153374269
|
C | T | 1 | a0001c0002t0003g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.276+15647C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153374269 | ||||||
chr4:153374317
|
G | A | 26 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(23): Show | 27 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.276+15695G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153374317 | ||||||
chr4:153374393
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.276+15771G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153374393 | ||||||
chr4:153374544
|
G | A | 1 | a0001c0002t0003g0127 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.276+15922G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153374544 | ||||||
chr4:153374577
|
T | C | 3 | a0001c0002t0003g0011a0001c0002t0003g0012a0001c0002t0003g0013 | 3 | HG01243.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.276+15955T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153374577 | ||||||
chr4:153374668
|
G | A | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.276+16046G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153374668 | ||||||
chr4:153374821
|
G | A | 8 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(5): Show | 8 | HG01516.hp1 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.276+16199G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153374821 | ||||||
chr4:153374834
|
G | A | 2 | a0001c0001t0003g0189a0001c0002t0003g0131 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.276+16212G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153374834 | ||||||
chr4:153374856
|
C | G | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.276+16234C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153374856 | ||||||
chr4:153374948
|
A | T | 26 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(23): Show | 27 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.276+16326A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153374948 | ||||||
chr4:153375118
|
T | C | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0104 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.276+16496T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153375118 | ||||||
chr4:153375216
|
G | T | 106 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(103): Show | 108 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.276+16594G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153375216 | ||||||
chr4:153375315
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.276+16693A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153375315 | ||||||
chr4:153375327
|
A | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.276+16705A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153375327 | ||||||
chr4:153375331
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.276+16709C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153375331 | ||||||
chr4:153375375
|
C | G | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.276+16753C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153375375 | ||||||
chr4:153375643
|
T | C | 21 | a0001c0001t0003g0048a0001c0002t0003g0011a0001c0002t0003g0012others(18): Show | 22 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.276+17021T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153375643 | ||||||
chr4:153375689
|
A | G | 4 | a0001c0001t0002g0312a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG01243.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+17067A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153375689 | ||||||
chr4:153375731
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.276+17109A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153375731 | ||||||
chr4:153375955
|
T | G | 2 | a0001c0001t0003g0189a0001c0002t0003g0131 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.276+17333T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153375955 | ||||||
chr4:153376068
|
C | G | 1 | a0001c0001t0001g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.276+17446C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153376068 | ||||||
chr4:153376079
|
G | A | 2 | a0001c0001t0002g0091a0001c0001t0002g0092 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.276+17457G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153376079 | ||||||
chr4:153376083
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.276+17461G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153376083 | ||||||
chr4:153376249
|
G | A | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.276+17627G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153376249 | ||||||
chr4:153376333
|
G | T | 2 | a0001c0001t0002g0091a0001c0001t0002g0092 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.276+17711G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153376333 | ||||||
chr4:153376415
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.276+17793C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153376415 | ||||||
chr4:153376579
|
T | C | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0104 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.277-17683T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153376579 | ||||||
chr4:153376601
|
C | T | 2 | a0001c0001t0003g0189a0001c0002t0003g0131 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.277-17661C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153376601 | ||||||
chr4:153376695
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.277-17567A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153376695 | ||||||
chr4:153376716
|
C | G | 3 | a0001c0002t0003g0011a0001c0002t0003g0012a0001c0002t0003g0013 | 3 | HG01243.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.277-17546C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153376716 | ||||||
chr4:153376817
|
A | G | 1 | a0001c0002t0003g0131 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.277-17445A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153376817 | ||||||
chr4:153377221
|
G | A | 3 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG02280.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.277-17041G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153377221 | ||||||
chr4:153377439
|
A | G | 2 | a0001c0001t0003g0189a0001c0002t0003g0131 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.277-16823A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153377439 | ||||||
chr4:153377874
|
T | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0027 | 3 | NA18939.hp2 NA18954.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.277-16388T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153377874 | ||||||
chr4:153377906
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.277-16356T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153377906 | ||||||
chr4:153377922
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 82 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.277-16340T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153377922 | ||||||
chr4:153377982
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.277-16280T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153377982 | ||||||
chr4:153378046
|
A | C | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-16216A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153378046 | ||||||
chr4:153378060
|
A | G | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-16202A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153378060 | ||||||
chr4:153378117
|
C | T | 80 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(77): Show | 82 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.277-16145C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153378117 | ||||||
chr4:153378148
|
T | C | 8 | a0001c0001t0002g0326a0001c0001t0002g0327a0001c0001t0002g0329others(5): Show | 8 | HG02055.hp1 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.277-16114T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153378148 | ||||||
chr4:153378677
|
C | T | 24 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(21): Show | 25 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.277-15585C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153378677 | ||||||
chr4:153378805
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.277-15457G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153378805 | ||||||
chr4:153378894
|
A | G | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-15368A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153378894 | ||||||
chr4:153379289
|
CA | C | 97 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0002g0005others(94): Show | 100 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.277-14958delA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153379289 | |||||
chr4:153379325
|
GA | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(36): Show | 40 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.277-14926delA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153379325 | |||||
chr4:153379480
|
A | C | 1 | a0001c0001t0002g0249 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.277-14782A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153379480 | ||||||
chr4:153379539
|
A | AAAAT | 13 | a0001c0001t0001g0214a0001c0001t0003g0048a0001c0002t0003g0090others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.277-14704_277-1470 others(8): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153379539 | |||||
chr4:153379634
|
G | A | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(2): Show | 5 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-14628G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153379634 | ||||||
chr4:153379678
|
C | T | 82 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(79): Show | 84 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.277-14584C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153379678 | ||||||
chr4:153379822
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.277-14440C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153379822 | ||||||
chr4:153379849
|
C | CA | 15 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0086others(12): Show | 15 | HG00642.hp2 HG00735.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.277-14386dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153379849 | |||||
chr4:153379849
|
CA | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.277-14386delA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153379849 | |||||
chr4:153379849
|
CAA | C | 101 | a0001c0001t0001g0080a0001c0001t0001g0102a0001c0001t0002g0005others(98): Show | 103 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.277-14387_277-1438 others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153379849 | |||||
chr4:153379863
|
A | C | 22 | a0001c0001t0003g0048a0001c0002t0003g0011a0001c0002t0003g0012others(19): Show | 23 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.277-14399A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153379863 | ||||||
chr4:153379877
|
T | C | 130 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(127): Show | 133 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.277-14385T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153379877 | ||||||
chr4:153379969
|
CTA | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(35): Show | 40 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.277-14291_277-1429 others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153379969 | |||||
chr4:153380080
|
G | GTTA | 335 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(332): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.277-14181_277-1418 others(7): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153380080 | |||||
chr4:153380082
|
G | T | 335 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(332): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.277-14180G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153380082 | ||||||
chr4:153380083
|
G | C | 335 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(332): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.277-14179G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153380083 | ||||||
chr4:153380335
|
T | A | 1 | a0001c0002t0003g0131 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.277-13927T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153380335 | ||||||
chr4:153380413
|
G | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | HG02523.hp2 NA19004.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.277-13849G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153380413 | ||||||
chr4:153380549
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.277-13713G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153380549 | ||||||
chr4:153380760
|
T | G | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-13502T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153380760 | ||||||
chr4:153380765
|
C | T | 130 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(127): Show | 133 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.277-13497C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153380765 | ||||||
chr4:153380870
|
A | T | 1 | a0001c0001t0001g0137 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.277-13392A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153380870 | ||||||
chr4:153380905
|
G | GT | 109 | a0001c0001t0001g0209a0001c0001t0002g0005a0001c0001t0002g0006others(106): Show | 112 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.277-13345dupT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153380905 | |||||
chr4:153381045
|
G | A | 8 | a0001c0001t0001g0144a0001c0001t0001g0149a0001c0001t0001g0154others(5): Show | 8 | HG00558.hp1 HG01496.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.277-13217G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381045 | ||||||
chr4:153381121
|
G | A | 82 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(79): Show | 84 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.277-13141G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381121 | ||||||
chr4:153381142
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.277-13120G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381142 | ||||||
chr4:153381181
|
C | G | 189 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 193 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.277-13081C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381181 | ||||||
chr4:153381186
|
A | C | 47 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0082others(44): Show | 49 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.277-13076A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381186 | ||||||
chr4:153381383
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.277-12879T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381383 | ||||||
chr4:153381558
|
AATTG | A | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(2): Show | 5 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-12703_277-1270 others(8): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381558 | ||||||
chr4:153381559
|
A | T | 183 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(180): Show | 187 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.277-12703A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381559 | ||||||
chr4:153381580
|
C | T | 1 | a0001c0002t0003g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.277-12682C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381580 | ||||||
chr4:153381667
|
A | AAT | 8 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0145others(5): Show | 8 | HG00323.hp2 HG01109.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.277-12570_277-1256 others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381667 | |||||
chr4:153381667
|
A | AATAT | 25 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(22): Show | 25 | HG00597.hp2 HG01167.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.277-12572_277-1256 others(8): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381667 | |||||
chr4:153381667
|
A | AATATAT | 9 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0078others(6): Show | 9 | HG00140.hp1 HG02027.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.277-12574_277-1256 others(10): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381667 | |||||
chr4:153381667
|
A | AATATATA others(1): Show |
10 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0033others(7): Show | 11 | HG02056.hp2 HG02074.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.277-12576_277-1256 others(12): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381667 | |||||
chr4:153381667
|
A | AATATATA others(3): Show |
6 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 6 | HG00735.hp1 HG01109.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.277-12578_277-1256 others(14): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381667 | |||||
chr4:153381667
|
A | AATATATA others(5): Show |
5 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0024others(2): Show | 5 | HG00609.hp1 HG01934.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-12580_277-1256 others(16): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381667 | |||||
chr4:153381667
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0183 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.277-12582_277-1256 others(18): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381667 | |||||
chr4:153381667
|
A | AATATATA others(11): Show |
2 | a0001c0001t0001g0037a0001c0001t0001g0051 | 2 | HG01081.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.277-12586_277-1256 others(22): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381667 | |||||
chr4:153381667
|
A | AATATATA others(13): Show |
1 | a0001c0001t0001g0027 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.277-12588_277-1256 others(24): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381667 | |||||
chr4:153381667
|
A | AATATATA others(34): Show |
1 | a0001c0001t0001g0075 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.277-12574_277-1257 others(45): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381667 | |||||
chr4:153381667
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0023 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.277-12595_277-1259 others(15): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381667 | ||||||
chr4:153381667
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0043 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.277-12595_277-1259 others(17): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381667 | ||||||
chr4:153381667
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0025 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.277-12595_277-1259 others(21): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381667 | ||||||
chr4:153381667
|
A | T | 1 | a0001c0001t0001g0232 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.277-12595A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381667 | ||||||
chr4:153381668
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.277-12593_277-1257 others(19): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381668 | |||||
chr4:153381672
|
AT | A | 6 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(3): Show | 6 | HG02647.hp1 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.277-12589delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381672 | ||||||
chr4:153381672
|
ATAT | A | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065 | 3 | HG02257.hp2 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.277-12589_277-1258 others(7): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381672 | ||||||
chr4:153381679
|
T | TA | 5 | a0001c0001t0002g0327a0001c0001t0002g0329a0001c0001t0002g0330others(2): Show | 5 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-12582dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381679 | |||||
chr4:153381679
|
T | TAATATAT others(188): Show |
2 | a0001c0001t0002g0300a0001c0001t0002g0301 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.277-12582_277-1258 others(199): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381679 | |||||
chr4:153381679
|
T | TAATATAT others(156): Show |
1 | a0001c0001t0002g0279 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.277-12582_277-1258 others(167): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381679 | |||||
chr4:153381679
|
T | TAATATAT others(132): Show |
1 | a0001c0001t0002g0326 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.277-12582_277-1258 others(143): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381679 | |||||
chr4:153381679
|
T | TAATATAT others(130): Show |
2 | a0001c0001t0002g0332a0001c0001t0002g0333 | 2 | HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.277-12582_277-1258 others(141): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381679 | |||||
chr4:153381679
|
T | TAATATAT others(152): Show |
1 | a0001c0001t0002g0336 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.277-12582_277-1258 others(163): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381679 | |||||
chr4:153381679
|
T | TAATATAT others(157): Show |
1 | a0001c0001t0002g0331 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.277-12582_277-1258 others(168): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381679 | |||||
chr4:153381679
|
T | TATAATAT others(190): Show |
3 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289 | 3 | NA18945.hp2 NA18946.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.277-12580_277-1257 others(201): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381679 | |||||
chr4:153381679
|
T | TATTATAT others(129): Show |
1 | a0001c0001t0002g0320 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.277-12581_277-1258 others(140): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381679 | |||||
chr4:153381679
|
T | TTATAATA others(124): Show |
1 | a0001c0001t0001g0108 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.277-12583_277-1258 others(135): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381679 | ||||||
chr4:153381679
|
T | TTATAATA others(129): Show |
5 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(2): Show | 5 | HG02055.hp2 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-12583_277-1258 others(140): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381679 | ||||||
chr4:153381679
|
T | TTATAATA others(159): Show |
1 | a0001c0001t0001g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.277-12583_277-1258 others(170): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381679 | ||||||
chr4:153381681
|
T | TAATATAT others(188): Show |
2 | a0001c0001t0002g0274a0001c0001t0002g0281 | 2 | NA18980.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.277-12580_277-1257 others(199): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(159): Show |
1 | a0001c0001t0002g0318 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.277-12580_277-1257 others(170): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(157): Show |
4 | a0002c0004t0002g0273a0002c0004t0002g0290a0002c0004t0002g0291others(1): Show | 4 | HG00408.hp2 NA18987.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-12580_277-1257 others(168): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(154): Show |
1 | a0001c0001t0002g0304 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.277-12580_277-1257 others(165): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(161): Show |
15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0264others(12): Show | 17 | HG00323.hp1 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.277-12580_277-1257 others(172): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(157): Show |
1 | a0001c0001t0002g0115 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.277-12580_277-1257 others(168): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(157): Show |
1 | a0001c0001t0002g0262 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.277-12580_277-1257 others(168): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(185): Show |
1 | a0001c0001t0002g0280 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.277-12580_277-1257 others(196): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(190): Show |
1 | a0001c0001t0002g0316 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.277-12580_277-1257 others(201): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(215): Show |
1 | a0001c0001t0002g0297 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.277-12580_277-1257 others(226): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(152): Show |
1 | a0001c0001t0002g0293 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.277-12580_277-1257 others(163): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(161): Show |
1 | a0001c0001t0002g0314 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.277-12580_277-1257 others(172): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(125): Show |
1 | a0001c0001t0002g0087 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.277-12580_277-1257 others(136): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(130): Show |
1 | a0001c0001t0002g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.277-12580_277-1257 others(141): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(130): Show |
2 | a0001c0001t0002g0306a0001c0001t0002g0307 | 2 | NA18952.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.277-12580_277-1257 others(141): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(100): Show |
1 | a0001c0001t0002g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.277-12580_277-1257 others(111): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(127): Show |
1 | a0001c0001t0002g0275 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.277-12580_277-1257 others(138): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(132): Show |
12 | a0001c0001t0002g0267a0001c0001t0002g0271a0001c0001t0002g0276others(9): Show | 12 | HG00642.hp1 HG02074.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.277-12580_277-1257 others(143): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(130): Show |
2 | a0001c0001t0002g0113a0001c0001t0002g0114 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.277-12580_277-1257 others(141): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(115): Show |
1 | a0001c0001t0002g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.277-12580_277-1257 others(126): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TAATATAT others(132): Show |
1 | a0001c0001t0002g0315 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.277-12580_277-1257 others(143): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381681 | |||||
chr4:153381681
|
T | TTATATAT others(134): Show |
1 | a0001c0001t0002g0284 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.277-12581_277-1258 others(145): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381681 | ||||||
chr4:153381682
|
A | AATATATA others(157): Show |
1 | a0001c0001t0002g0272 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.277-12580_277-1257 others(168): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381682 | ||||||
chr4:153381682
|
A | AATATATA others(157): Show |
1 | a0001c0001t0002g0263 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.277-12580_277-1257 others(168): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381682 | ||||||
chr4:153381682
|
A | AATATATA others(159): Show |
1 | a0001c0001t0002g0266 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.277-12580_277-1257 others(170): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381682 | ||||||
chr4:153381682
|
A | AATATATA others(182): Show |
1 | a0001c0001t0002g0309 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.277-12580_277-1257 others(193): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381682 | ||||||
chr4:153381682
|
A | AATATATA others(130): Show |
1 | a0001c0001t0002g0328 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.277-12580_277-1257 others(141): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381682 | ||||||
chr4:153381682
|
A | AATATATA others(132): Show |
4 | a0001c0001t0002g0321a0001c0001t0002g0322a0001c0001t0002g0323others(1): Show | 4 | HG01891.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-12580_277-1257 others(143): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381682 | ||||||
chr4:153381682
|
A | AATATATA others(130): Show |
2 | a0001c0001t0002g0294a0001c0001t0002g0311 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.277-12580_277-1257 others(141): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381682 | ||||||
chr4:153381683
|
T | A | 11 | a0001c0001t0002g0263a0001c0001t0002g0266a0001c0001t0002g0272others(8): Show | 11 | HG00597.hp1 HG01891.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.277-12579T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381683 | ||||||
chr4:153381683
|
T | TA | 4 | a0001c0001t0001g0108a0001c0001t0002g0279a0001c0001t0002g0320others(1): Show | 4 | HG02148.hp1 HG02965.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-12578dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381683 | |||||
chr4:153381685
|
T | TA | 4 | a0001c0001t0002g0014a0001c0001t0002g0087a0001c0001t0002g0275others(1): Show | 4 | HG06807.hp2 NA18951.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-12576dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381685 | |||||
chr4:153381685
|
T | TATAATAT others(125): Show |
5 | a0001c0001t0002g0327a0001c0001t0002g0329a0001c0001t0002g0330others(2): Show | 5 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-12574_277-1257 others(136): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381685 | |||||
chr4:153381686
|
ATATATAT others(9): Show |
A | 1 | a0001c0002t0003g0120 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.277-12574_277-1255 others(20): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381686 | |||||
chr4:153381686
|
ATATATAT others(11): Show |
A | 1 | a0001c0002t0003g0090 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.277-12574_277-1255 others(22): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381686 | |||||
chr4:153381688
|
ATATATTT others(9): Show |
A | 2 | a0001c0002t0003g0118a0001c0002t0003g0119 | 2 | HG02083.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.277-12572_277-1255 others(20): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381688 | |||||
chr4:153381688
|
ATATATTT others(10): Show |
A | 2 | a0001c0002t0003g0117a0001c0002t0003g0130 | 2 | HG02735.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.277-12572_277-1255 others(21): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381688 | |||||
chr4:153381688
|
ATATATTT others(11): Show |
A | 1 | a0001c0002t0003g0131 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.277-12572_277-1255 others(22): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381688 | |||||
chr4:153381690
|
ATATTTTT others(7): Show |
A | 6 | a0001c0001t0003g0048a0001c0002t0003g0116a0001c0002t0003g0121others(3): Show | 6 | HG01071.hp2 HG01081.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.277-12570_277-1255 others(18): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381690 | |||||
chr4:153381690
|
ATATTTTT others(8): Show |
A | 1 | a0001c0002t0003g0122 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.277-12570_277-1255 others(19): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381690 | |||||
chr4:153381690
|
ATATTTTT others(10): Show |
A | 3 | a0001c0002t0003g0127a0001c0002t0003g0128a0001c0003t0004g0004 | 4 | HG01884.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-12570_277-1255 others(21): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381690 | |||||
chr4:153381692
|
A | ATATAT | 6 | a0001c0001t0001g0003a0001c0001t0001g0080a0001c0001t0001g0135others(3): Show | 7 | HG01074.hp2 HG01106.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.277-12569_277-1256 others(9): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381692 | |||||
chr4:153381692
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.277-12569_277-1256 others(17): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381692 | |||||
chr4:153381692
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0026 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.277-12569_277-1256 others(28): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381692 | |||||
chr4:153381692
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0020 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.277-12569_277-1256 others(28): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381692 | |||||
chr4:153381692
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.277-12569_277-1256 others(15): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381692 | |||||
chr4:153381692
|
A | ATATT | 15 | a0001c0001t0001g0053a0001c0001t0001g0139a0001c0001t0001g0149others(12): Show | 15 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.277-12569_277-1256 others(8): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381692 | |||||
chr4:153381692
|
A | ATATTT | 8 | a0001c0001t0001g0155a0001c0001t0001g0172a0001c0001t0001g0180others(5): Show | 8 | HG01934.hp2 HG02132.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.277-12569_277-1256 others(9): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381692 | |||||
chr4:153381692
|
AT | A | 17 | a0001c0001t0001g0070a0001c0001t0001g0097a0001c0001t0002g0005others(14): Show | 19 | HG00323.hp1 HG00408.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.277-12539delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381692 | |||||
chr4:153381692
|
ATTT | A | 45 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(42): Show | 45 | HG00642.hp1 HG01515.hp1 HG01516.hp1 others(42): Show |
intron_variant | MODIFIER | c.277-12541_277-1253 others(7): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381692 | |||||
chr4:153381692
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0002t0003g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.277-12549_277-1253 others(15): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381692 | |||||
chr4:153381692
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.277-12551_277-1253 others(17): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381692 | |||||
chr4:153381692
|
ATTTTTTT others(7): Show |
A | 3 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG02280.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.277-12552_277-1253 others(18): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381692 | |||||
chr4:153381692
|
ATTTTTTT others(8): Show |
A | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-12553_277-1253 others(19): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381692 | |||||
chr4:153381692
|
ATTTTTTT others(9): Show |
A | 2 | a0001c0001t0002g0091a0001c0001t0002g0092 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.277-12554_277-1253 others(20): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381692 | |||||
chr4:153381692
|
ATTTTTTT others(10): Show |
A | 2 | a0001c0003t0004g0099a0001c0003t0004g0100 | 2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.277-12555_277-1253 others(21): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153381692 | |||||
chr4:153381693
|
T | A | 1 | a0001c0001t0002g0265 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.277-12569T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381693 | ||||||
chr4:153381693
|
T | TA | 24 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0025others(21): Show | 24 | HG00558.hp2 HG01346.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.277-12569_277-1256 others(5): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381693 | ||||||
chr4:153381693
|
T | TATA | 13 | a0001c0001t0001g0074a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 13 | HG00099.hp2 HG00741.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.277-12569_277-1256 others(7): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381693 | ||||||
chr4:153381693
|
T | TATATA | 5 | a0001c0001t0001g0176a0001c0001t0001g0185a0001c0001t0001g0202others(2): Show | 5 | HG00621.hp1 HG00621.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-12569_277-1256 others(9): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381693 | ||||||
chr4:153381693
|
T | TATATATA | 8 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0030others(5): Show | 8 | HG01070.hp2 HG01256.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.277-12569_277-1256 others(11): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381693 | ||||||
chr4:153381693
|
T | TATATATA others(2): Show |
10 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0028others(7): Show | 10 | HG02523.hp2 HG03491.hp1 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.277-12569_277-1256 others(13): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381693 | ||||||
chr4:153381693
|
T | TATATATA others(4): Show |
12 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0132others(9): Show | 12 | HG00609.hp2 HG01123.hp1 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.277-12569_277-1256 others(15): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381693 | ||||||
chr4:153381693
|
T | TATATATA others(12): Show |
1 | a0001c0001t0001g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.277-12569_277-1256 others(23): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381693 | ||||||
chr4:153381694
|
T | A | 66 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0018others(63): Show | 66 | HG00597.hp1 HG01081.hp2 HG01169.hp2 others(63): Show |
intron_variant | MODIFIER | c.277-12568T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381694 | ||||||
chr4:153381695
|
T | A | 67 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(64): Show | 69 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.277-12567T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381695 | ||||||
chr4:153381696
|
T | A | 44 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0049others(41): Show | 44 | HG00597.hp1 HG01169.hp2 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.277-12566T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381696 | ||||||
chr4:153381697
|
T | A | 89 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(86): Show | 91 | HG00323.hp1 HG00408.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.277-12565T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381697 | ||||||
chr4:153381698
|
T | A | 41 | a0001c0001t0001g0018a0001c0001t0001g0061a0001c0001t0001g0062others(38): Show | 41 | HG00597.hp1 HG01169.hp2 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.277-12564T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381698 | ||||||
chr4:153381699
|
T | A | 75 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(72): Show | 77 | HG00323.hp1 HG00408.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.277-12563T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381699 | ||||||
chr4:153381700
|
T | A | 33 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0065others(30): Show | 33 | HG00597.hp1 HG01169.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.277-12562T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381700 | ||||||
chr4:153381701
|
T | A | 70 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(67): Show | 72 | HG00323.hp1 HG00408.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.277-12561T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381701 | ||||||
chr4:153381702
|
T | A | 28 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0089others(25): Show | 28 | HG00597.hp1 HG01496.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.277-12560T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381702 | ||||||
chr4:153381703
|
T | A | 67 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(64): Show | 69 | HG00323.hp1 HG00408.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.277-12559T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381703 | ||||||
chr4:153381704
|
T | A | 24 | a0001c0001t0001g0108a0001c0001t0002g0014a0001c0001t0002g0087others(21): Show | 24 | HG00597.hp1 HG01496.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.277-12558T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381704 | ||||||
chr4:153381705
|
T | A | 65 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(62): Show | 67 | HG00323.hp1 HG00408.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.277-12557T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381705 | ||||||
chr4:153381706
|
T | A | 24 | a0001c0001t0001g0108a0001c0001t0002g0014a0001c0001t0002g0087others(21): Show | 24 | HG00597.hp1 HG01496.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.277-12556T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381706 | ||||||
chr4:153381707
|
T | A | 57 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0082others(54): Show | 59 | HG00323.hp1 HG00408.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.277-12555T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381707 | ||||||
chr4:153381708
|
T | A | 21 | a0001c0001t0002g0014a0001c0001t0002g0087a0001c0001t0002g0263others(18): Show | 21 | HG00597.hp1 HG01496.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.277-12554T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381708 | ||||||
chr4:153381709
|
T | A | 32 | a0001c0001t0002g0082a0001c0001t0002g0112a0001c0001t0002g0113others(29): Show | 32 | HG00408.hp2 HG00741.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.277-12553T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381709 | ||||||
chr4:153381709
|
T | TATATATA others(129): Show |
1 | a0001c0001t0002g0265 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.277-12553_277-1255 others(140): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381709 | ||||||
chr4:153381710
|
T | A | 12 | a0001c0001t0002g0087a0001c0001t0002g0091a0001c0001t0002g0092others(9): Show | 12 | HG02148.hp1 HG02895.hp2 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.277-12552T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381710 | ||||||
chr4:153381711
|
T | A | 1 | a0001c0001t0002g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.277-12551T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381711 | ||||||
chr4:153381712
|
T | A | 5 | a0001c0001t0002g0266a0001c0001t0002g0287a0001c0001t0002g0288others(2): Show | 5 | NA18945.hp2 NA18946.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-12550T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381712 | ||||||
chr4:153381714
|
T | A | 1 | a0001c0001t0002g0266 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.277-12548T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381714 | ||||||
chr4:153381822
|
G | A | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-12440G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381822 | ||||||
chr4:153381864
|
T | C | 3 | a0001c0003t0004g0004a0001c0003t0004g0099a0001c0003t0004g0100 | 4 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-12398T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381864 | ||||||
chr4:153381881
|
A | G | 22 | a0001c0001t0003g0048a0001c0002t0003g0011a0001c0002t0003g0012others(19): Show | 23 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.277-12381A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381881 | ||||||
chr4:153381962
|
G | A | 2 | a0001c0002t0003g0130a0001c0002t0003g0131 | 2 | HG01891.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.277-12300G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153381962 | ||||||
chr4:153382342
|
A | G | 1 | a0001c0002t0003g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.277-11920A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153382342 | ||||||
chr4:153382356
|
G | A | 1 | a0001c0001t0002g0315 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.277-11906G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153382356 | ||||||
chr4:153382555
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.277-11707A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153382555 | ||||||
chr4:153382629
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.277-11633C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153382629 | ||||||
chr4:153382805
|
T | A | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.277-11457T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153382805 | ||||||
chr4:153382897
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.277-11365G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153382897 | ||||||
chr4:153382970
|
T | C | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.277-11292T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153382970 | ||||||
chr4:153383395
|
C | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(11): Show | 15 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.277-10867C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153383395 | ||||||
chr4:153383397
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 137 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.277-10865G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153383397 | ||||||
chr4:153383424
|
G | A | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-10838G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153383424 | ||||||
chr4:153383556
|
C | G | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-10706C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153383556 | ||||||
chr4:153383694
|
T | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0169 | 2 | NA18963.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.277-10568T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153383694 | ||||||
chr4:153383824
|
A | T | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(2): Show | 5 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-10438A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153383824 | ||||||
chr4:153383931
|
T | G | 1 | a0001c0003t0004g0100 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.277-10331T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153383931 | ||||||
chr4:153383979
|
A | T | 2 | a0001c0001t0002g0243a0001c0001t0002g0246 | 2 | NA18942.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.277-10283A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153383979 | ||||||
chr4:153384112
|
A | G | 82 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(79): Show | 84 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.277-10150A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153384112 | ||||||
chr4:153384258
|
C | CT | 68 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0035others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.277-9977dupT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384258 | |||||
chr4:153384258
|
C | CTT | 13 | a0001c0001t0001g0088a0001c0001t0001g0134a0001c0001t0001g0143others(10): Show | 13 | HG00597.hp2 HG02040.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.277-9978_277-9977d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384258 | |||||
chr4:153384258
|
CT | C | 61 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0016others(58): Show | 62 | HG00099.hp1 HG00140.hp1 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.277-9977delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384258 | |||||
chr4:153384258
|
CTT | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0084others(4): Show | 7 | HG01070.hp2 HG01993.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-9978_277-9977d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384258 | |||||
chr4:153384258
|
CTTTTTTT others(2): Show |
C | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-9985_277-9977d others(11): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384258 | |||||
chr4:153384401
|
CT | C | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-9860delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153384401 | ||||||
chr4:153384443
|
A | AT | 19 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0105others(16): Show | 19 | HG00099.hp2 HG00140.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-9790dupT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384443 | |||||
chr4:153384443
|
A | ATTTTTTT | 7 | a0001c0001t0002g0014a0001c0001t0002g0082a0001c0001t0002g0320others(4): Show | 7 | HG01891.hp2 HG02148.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-9796_277-9790d others(9): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384443 | |||||
chr4:153384443
|
A | ATTTTTTT others(1): Show |
19 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0087others(16): Show | 21 | HG00323.hp1 HG01074.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.277-9797_277-9790d others(10): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384443 | |||||
chr4:153384443
|
A | ATTTTTTT others(2): Show |
25 | a0001c0001t0002g0113a0001c0001t0002g0263a0001c0001t0002g0265others(22): Show | 25 | HG00597.hp1 HG01069.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.277-9798_277-9790d others(11): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384443 | |||||
chr4:153384443
|
A | ATTTTTTT others(3): Show |
12 | a0001c0001t0002g0112a0001c0001t0002g0114a0001c0001t0002g0271others(9): Show | 12 | HG00408.hp2 HG00642.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.277-9799_277-9790d others(12): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384443 | |||||
chr4:153384443
|
A | ATTTTTTT others(4): Show |
4 | a0001c0001t0002g0274a0001c0001t0002g0280a0001c0001t0002g0281others(1): Show | 4 | NA18951.hp1 NA18960.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-9800_277-9790d others(13): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384443 | |||||
chr4:153384443
|
AT | A | 27 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0040others(24): Show | 27 | HG01169.hp2 HG01255.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.277-9790delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384443 | |||||
chr4:153384443
|
ATT | A | 37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(34): Show | 39 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.277-9791_277-9790d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384443 | |||||
chr4:153384443
|
ATTT | A | 18 | a0001c0001t0001g0017a0001c0001t0002g0044a0001c0001t0002g0045others(15): Show | 18 | HG01256.hp1 HG03017.hp1 NA18942.hp2 others(15): Show |
intron_variant | MODIFIER | c.277-9792_277-9790d others(5): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384443 | |||||
chr4:153384443
|
ATTTTTTT others(1): Show |
A | 12 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(9): Show | 13 | HG00099.hp1 HG00140.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.277-9797_277-9790d others(10): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384443 | |||||
chr4:153384443
|
ATTTTTTT others(5): Show |
A | 27 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(24): Show | 28 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.277-9801_277-9790d others(14): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384443 | |||||
chr4:153384443
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0190 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.277-9803_277-9790d others(16): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153384443 | |||||
chr4:153384546
|
G | A | 1 | a0001c0001t0002g0293 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.277-9716G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153384546 | ||||||
chr4:153384594
|
A | G | 116 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(113): Show | 119 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.277-9668A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153384594 | ||||||
chr4:153384639
|
C | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-9623C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153384639 | ||||||
chr4:153384649
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.277-9613G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153384649 | ||||||
chr4:153384698
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.277-9564T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153384698 | ||||||
chr4:153384742
|
C | G | 1 | a0001c0001t0001g0166 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.277-9520C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153384742 | ||||||
chr4:153384885
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-9377G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153384885 | ||||||
chr4:153384969
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.277-9293G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153384969 | ||||||
chr4:153385228
|
G | C | 1 | a0001c0001t0001g0209 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.277-9034G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153385228 | ||||||
chr4:153385401
|
A | G | 137 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(134): Show | 140 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.277-8861A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153385401 | ||||||
chr4:153385525
|
G | A | 11 | a0001c0001t0001g0088a0001c0001t0001g0093a0001c0001t0001g0094others(8): Show | 11 | HG01255.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.277-8737G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153385525 | ||||||
chr4:153385605
|
GCTCAGGA others(69): Show |
G | 1 | a0001c0001t0001g0043 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.277-8653_277-8578d others(78): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153385605 | |||||
chr4:153385715
|
C | CA | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 110 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.277-8528dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153385715 | |||||
chr4:153385730
|
A | AG | 4 | a0001c0001t0001g0103a0001c0003t0004g0004a0001c0003t0004g0099others(1): Show | 5 | HG01255.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-8532_277-8531i others(3): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153385730 | ||||||
chr4:153385730
|
A | G | 19 | a0001c0001t0003g0048a0001c0002t0003g0011a0001c0002t0003g0012others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.277-8532A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153385730 | ||||||
chr4:153385733
|
A | G | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-8529A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153385733 | ||||||
chr4:153385735
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-8527G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153385735 | ||||||
chr4:153385762
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.277-8500G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153385762 | ||||||
chr4:153385775
|
A | T | 3 | a0001c0003t0004g0004a0001c0003t0004g0099a0001c0003t0004g0100 | 4 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-8487A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153385775 | ||||||
chr4:153385897
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-8365G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153385897 | ||||||
chr4:153386246
|
T | C | 1 | a0001c0001t0002g0247 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.277-8016T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153386246 | ||||||
chr4:153386316
|
A | C | 137 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(134): Show | 140 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.277-7946A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153386316 | ||||||
chr4:153386459
|
G | C | 2 | a0001c0002t0003g0124a0001c0002t0003g0125 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.277-7803G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153386459 | ||||||
chr4:153386590
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.277-7672C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153386590 | ||||||
chr4:153386714
|
TCAA | T | 11 | a0001c0001t0001g0088a0001c0001t0001g0093a0001c0001t0001g0094others(8): Show | 11 | HG01255.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.277-7532_277-7530d others(5): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153386714 | |||||
chr4:153386733
|
A | C | 1 | a0001c0001t0001g0202 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.277-7529A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153386733 | ||||||
chr4:153386916
|
G | T | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(2): Show | 5 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-7346G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153386916 | ||||||
chr4:153386997
|
C | T | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-7265C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153386997 | ||||||
chr4:153387101
|
A | G | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-7161A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153387101 | ||||||
chr4:153387235
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.277-7027C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153387235 | ||||||
chr4:153387629
|
G | A | 1 | a0001c0001t0002g0313 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.277-6633G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153387629 | ||||||
chr4:153387672
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-6590G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153387672 | ||||||
chr4:153387683
|
T | A | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.277-6579T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153387683 | ||||||
chr4:153387688
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-6574C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153387688 | ||||||
chr4:153387736
|
C | T | 1 | a0001c0001t0002g0241 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.277-6526C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153387736 | ||||||
chr4:153387837
|
CT | C | 6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.277-6415delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153387837 | |||||
chr4:153387847
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.277-6415T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153387847 | ||||||
chr4:153387864
|
G | A | 10 | a0001c0001t0003g0048a0001c0002t0003g0090a0001c0002t0003g0116others(7): Show | 10 | HG01081.hp1 HG01261.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.277-6398G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153387864 | ||||||
chr4:153387885
|
C | A | 16 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(13): Show | 16 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.277-6377C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153387885 | ||||||
chr4:153387887
|
G | C | 1 | a0001c0001t0001g0169 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.277-6375G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153387887 | ||||||
chr4:153387890
|
C | T | 14 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(11): Show | 14 | NA18942.hp2 NA18952.hp1 NA18968.hp1 others(11): Show |
intron_variant | MODIFIER | c.277-6372C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153387890 | ||||||
chr4:153388183
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.277-6079C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153388183 | ||||||
chr4:153388259
|
G | A | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-6003G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153388259 | ||||||
chr4:153388458
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.277-5804G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153388458 | ||||||
chr4:153388478
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.277-5784C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153388478 | ||||||
chr4:153388654
|
C | T | 130 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(127): Show | 133 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.277-5608C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153388654 | ||||||
chr4:153388681
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-5581C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153388681 | ||||||
chr4:153388867
|
G | C | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.277-5395G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153388867 | ||||||
chr4:153388885
|
C | T | 1 | a0001c0003t0004g0100 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.277-5377C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153388885 | ||||||
chr4:153388944
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.277-5318G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153388944 | ||||||
chr4:153389290
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.277-4972A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153389290 | ||||||
chr4:153389349
|
T | TTTTA | 3 | a0001c0001t0001g0162a0001c0001t0001g0188a0001c0001t0001g0215 | 3 | HG01123.hp2 HG01257.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.277-4891_277-4888d others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153389349 | |||||
chr4:153389413
|
T | G | 1 | a0001c0001t0002g0302 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.277-4849T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153389413 | ||||||
chr4:153389485
|
T | C | 35 | a0001c0001t0002g0014a0001c0001t0002g0265a0001c0001t0002g0267others(32): Show | 35 | HG00642.hp1 HG02055.hp1 HG02074.hp2 others(32): Show |
intron_variant | MODIFIER | c.277-4777T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153389485 | ||||||
chr4:153389564
|
T | C | 1 | a0001c0002t0003g0119 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.277-4698T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153389564 | ||||||
chr4:153389612
|
T | C | 27 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(24): Show | 28 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.277-4650T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153389612 | ||||||
chr4:153389687
|
C | A | 22 | a0001c0001t0003g0048a0001c0002t0003g0011a0001c0002t0003g0012others(19): Show | 23 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.277-4575C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153389687 | ||||||
chr4:153389870
|
T | A | 13 | a0001c0001t0002g0266a0001c0001t0002g0279a0001c0001t0002g0282others(10): Show | 13 | HG00408.hp2 HG01516.hp1 NA18945.hp2 others(10): Show |
intron_variant | MODIFIER | c.277-4392T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153389870 | ||||||
chr4:153389965
|
C | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0188a0001c0001t0001g0215 | 3 | HG01123.hp2 HG01257.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.277-4297C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153389965 | ||||||
chr4:153390030
|
C | CT | 7 | a0001c0001t0001g0022a0001c0001t0001g0038a0001c0001t0001g0074others(4): Show | 7 | HG01167.hp1 HG02027.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-4217dupT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390030 | |||||
chr4:153390030
|
CT | C | 137 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0171others(134): Show | 140 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.277-4217delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390030 | |||||
chr4:153390044
|
T | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0003t0004g0004others(2): Show | 6 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.277-4218T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390044 | ||||||
chr4:153390097
|
A | G | 7 | a0001c0001t0001g0053a0001c0001t0001g0075a0001c0001t0001g0076others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.277-4165A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390097 | ||||||
chr4:153390189
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 82 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.277-4073A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390189 | ||||||
chr4:153390316
|
A | G | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-3946A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390316 | ||||||
chr4:153390423
|
A | T | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.277-3839A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390423 | ||||||
chr4:153390432
|
A | G | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-3830A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390432 | ||||||
chr4:153390573
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.277-3689G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390573 | ||||||
chr4:153390622
|
T | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 125 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.277-3640T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390622 | ||||||
chr4:153390630
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-3632C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390630 | ||||||
chr4:153390859
|
C | G | 1 | a0003c0005t0002g0254 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.277-3403C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390859 | ||||||
chr4:153390889
|
A | ATATG | 3 | a0001c0001t0002g0294a0001c0001t0002g0311a0001c0001t0002g0329 | 3 | HG02630.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.277-3372_277-3371i others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390889 | |||||
chr4:153390889
|
A | ATATGTGT others(1): Show |
33 | a0001c0001t0002g0014a0001c0001t0002g0082a0001c0001t0002g0112others(30): Show | 33 | HG00642.hp1 HG01891.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.277-3372_277-3371i others(10): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390889 | |||||
chr4:153390889
|
A | ATATGTGT others(3): Show |
37 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0087others(34): Show | 39 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.277-3372_277-3371i others(12): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390889 | |||||
chr4:153390889
|
A | ATATGTGT others(5): Show |
5 | a0001c0001t0002g0113a0001c0001t0002g0332a0001c0001t0002g0333others(2): Show | 5 | HG02145.hp1 HG02922.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-3372_277-3371i others(14): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390889 | |||||
chr4:153390889
|
A | ATG | 3 | a0001c0001t0001g0156a0001c0001t0001g0198a0001c0001t0001g0217 | 3 | HG01928.hp2 HG02056.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.277-3347_277-3346d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390889 | |||||
chr4:153390889
|
A | ATGTG | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(2): Show | 5 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-3349_277-3346d others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390889 | |||||
chr4:153390889
|
A | G | 1 | a0001c0001t0002g0256 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.277-3373A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390889 | ||||||
chr4:153390889
|
ATG | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(41): Show | 45 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.277-3347_277-3346d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390889 | |||||
chr4:153390889
|
ATGTG | A | 13 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0057others(10): Show | 13 | HG01070.hp2 HG01123.hp2 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.277-3349_277-3346d others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390889 | |||||
chr4:153390891
|
G | A | 3 | a0001c0001t0002g0284a0001c0001t0002g0320a0001c0001t0002g0324 | 3 | HG01496.hp2 HG02148.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.277-3371G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390891 | ||||||
chr4:153390891
|
G | GTGTGTGT others(19): Show |
1 | a0001c0001t0001g0058 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.277-3350_277-3349i others(28): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390891 | |||||
chr4:153390897
|
GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0001g0199 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.277-3345_277-3324d others(24): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390897 | |||||
chr4:153390901
|
GTGTGTGT others(11): Show |
G | 2 | a0001c0001t0002g0284a0001c0001t0002g0320 | 2 | HG01496.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.277-3345_277-3328d others(20): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390901 | |||||
chr4:153390909
|
G | GTGTGTAT others(5): Show |
2 | a0001c0001t0002g0251a0001c0001t0002g0256 | 2 | NA18970.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.277-3348_277-3347i others(14): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390909 | |||||
chr4:153390911
|
G | GTGTATA | 2 | a0001c0003t0004g0004a0001c0003t0004g0099 | 3 | HG02896.hp2 HG02897.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.277-3348_277-3347i others(8): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390911 | |||||
chr4:153390913
|
G | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0016others(39): Show | 44 | HG00408.hp1 HG00558.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.277-3349G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390913 | ||||||
chr4:153390913
|
G | GTATA | 3 | a0001c0002t0003g0011a0001c0002t0003g0012a0001c0003t0004g0100 | 3 | HG02572.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.277-3348_277-3347i others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390913 | |||||
chr4:153390915
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(96): Show | 102 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.277-3347G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390915 | ||||||
chr4:153390917
|
A | G | 92 | a0001c0001t0001g0163a0001c0001t0002g0005a0001c0001t0002g0006others(89): Show | 95 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.277-3345A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390917 | ||||||
chr4:153390917
|
ATATGTGT others(1): Show |
A | 5 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 5 | HG01255.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-3343_277-3336d others(10): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390917 | |||||
chr4:153390919
|
A | ATATGTAT others(9): Show |
1 | a0001c0001t0002g0044 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.277-3342_277-3341i others(18): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390919 | |||||
chr4:153390919
|
A | ATG | 8 | a0001c0001t0001g0136a0001c0001t0001g0157a0001c0001t0001g0165others(5): Show | 8 | HG01928.hp1 HG01993.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.277-3321_277-3320d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390919 | |||||
chr4:153390919
|
A | ATGTATGT others(7): Show |
14 | a0001c0001t0002g0045a0001c0001t0002g0241a0001c0001t0002g0242others(11): Show | 14 | HG01256.hp1 HG03654.hp2 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.277-3340_277-3339i others(16): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390919 | |||||
chr4:153390919
|
A | ATGTATGT others(9): Show |
2 | a0001c0001t0002g0252a0001c0001t0002g0257 | 2 | HG03017.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.277-3340_277-3339i others(18): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390919 | |||||
chr4:153390919
|
A | ATGTG | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(3): Show | 6 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.277-3323_277-3320d others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390919 | |||||
chr4:153390919
|
A | ATGTGTG | 12 | a0001c0001t0003g0048a0001c0002t0003g0090a0001c0002t0003g0116others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.277-3325_277-3320d others(8): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390919 | |||||
chr4:153390919
|
A | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0016others(60): Show | 66 | HG00408.hp1 HG00558.hp2 HG01243.hp1 others(63): Show |
intron_variant | MODIFIER | c.277-3343A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390919 | ||||||
chr4:153390919
|
ATGTGTG | A | 6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.277-3325_277-3320d others(8): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153390919 | |||||
chr4:153390921
|
G | A | 80 | a0001c0001t0001g0057a0001c0001t0001g0239a0001c0001t0001g0240others(77): Show | 82 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.277-3341G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390921 | ||||||
chr4:153390943
|
A | G | 107 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(104): Show | 109 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.277-3319A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153390943 | ||||||
chr4:153391060
|
AT | A | 22 | a0001c0001t0003g0048a0001c0002t0003g0011a0001c0002t0003g0012others(19): Show | 23 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.277-3195delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153391060 | |||||
chr4:153391223
|
G | A | 1 | a0001c0001t0002g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.277-3039G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153391223 | ||||||
chr4:153391228
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 144 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.277-3034G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153391228 | ||||||
chr4:153391271
|
C | G | 1 | a0001c0001t0002g0309 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.277-2991C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153391271 | ||||||
chr4:153391313
|
G | A | 106 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(103): Show | 108 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.277-2949G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153391313 | ||||||
chr4:153391444
|
G | A | 7 | a0001c0001t0001g0053a0001c0001t0001g0075a0001c0001t0001g0076others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.277-2818G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153391444 | ||||||
chr4:153391463
|
C | T | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG02109.hp1 HG02886.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-2799C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153391463 | ||||||
chr4:153391495
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.277-2767G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153391495 | ||||||
chr4:153391683
|
C | T | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(2): Show | 5 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-2579C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153391683 | ||||||
chr4:153391727
|
T | TAC | 3 | a0001c0001t0001g0007a0001c0001t0001g0138a0001c0001t0001g0152 | 3 | HG01993.hp2 NA18959.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.277-2513_277-2512d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153391727 | |||||
chr4:153391727
|
T | TACACAC | 9 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(6): Show | 9 | HG02257.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.277-2517_277-2512d others(8): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153391727 | |||||
chr4:153391727
|
T | TACACACA others(3): Show |
29 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(26): Show | 30 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.277-2521_277-2512d others(12): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153391727 | |||||
chr4:153391727
|
T | TACACACA others(5): Show |
8 | a0001c0001t0001g0057a0001c0001t0001g0066a0001c0001t0001g0094others(5): Show | 8 | HG02280.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.277-2523_277-2512d others(14): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153391727 | |||||
chr4:153391727
|
T | TACACACA others(7): Show |
63 | a0001c0001t0001g0088a0001c0001t0001g0098a0001c0001t0001g0103others(60): Show | 65 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.277-2525_277-2512d others(16): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153391727 | |||||
chr4:153391727
|
T | TACACACA others(9): Show |
18 | a0001c0001t0001g0010a0001c0001t0001g0093a0001c0001t0001g0096others(15): Show | 19 | HG00408.hp2 HG02040.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.277-2527_277-2512d others(18): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153391727 | |||||
chr4:153391727
|
T | TACACACA others(11): Show |
27 | a0001c0001t0001g0027a0001c0001t0001g0036a0001c0001t0001g0095others(24): Show | 27 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.277-2529_277-2512d others(20): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153391727 | |||||
chr4:153391727
|
T | TACACACA others(13): Show |
29 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(26): Show | 31 | HG00408.hp1 HG01123.hp1 HG01516.hp2 others(28): Show |
intron_variant | MODIFIER | c.277-2531_277-2512d others(22): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153391727 | |||||
chr4:153391727
|
T | TACACACA others(15): Show |
27 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0021others(24): Show | 27 | HG00558.hp2 HG00735.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.277-2533_277-2512d others(24): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153391727 | |||||
chr4:153391727
|
T | TACACACA others(17): Show |
4 | a0001c0001t0001g0083a0001c0001t0002g0251a0001c0002t0003g0011others(1): Show | 4 | HG02572.hp2 HG03139.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-2512_277-2511i others(26): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153391727 | |||||
chr4:153391727
|
T | TACACACA others(19): Show |
5 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0108others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-2512_277-2511i others(28): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153391727 | |||||
chr4:153391727
|
T | TACACACA others(21): Show |
3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0002g0045 | 3 | HG03041.hp2 NA19030.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.277-2512_277-2511i others(30): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153391727 | |||||
chr4:153391727
|
T | TACACACA others(23): Show |
1 | a0001c0001t0001g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.277-2512_277-2511i others(32): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153391727 | |||||
chr4:153391751
|
T | C | 57 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(54): Show | 59 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.277-2511T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153391751 | ||||||
chr4:153391755
|
T | C | 1 | a0001c0002t0003g0117 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.277-2507T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153391755 | ||||||
chr4:153391778
|
AT | A | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-2474delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153391778 | |||||
chr4:153391877
|
A | G | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-2385A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153391877 | ||||||
chr4:153391952
|
A | C | 1 | a0001c0001t0001g0222 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.277-2310A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153391952 | ||||||
chr4:153391962
|
A | C | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.277-2300A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153391962 | ||||||
chr4:153392072
|
G | A | 1 | a0001c0001t0002g0320 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.277-2190G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392072 | ||||||
chr4:153392102
|
C | A | 1 | a0001c0001t0001g0205 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.277-2160C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392102 | ||||||
chr4:153392109
|
G | GT | 84 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(81): Show | 86 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.277-2143dupT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153392109 | |||||
chr4:153392249
|
A | C | 130 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(127): Show | 133 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.277-2013A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392249 | ||||||
chr4:153392296
|
G | A | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-1966G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392296 | ||||||
chr4:153392332
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-1930C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392332 | ||||||
chr4:153392347
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.277-1915G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392347 | ||||||
chr4:153392400
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.277-1862C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392400 | ||||||
chr4:153392429
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.277-1833A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392429 | ||||||
chr4:153392508
|
AT | A | 40 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(37): Show | 41 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.277-1748delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153392508 | |||||
chr4:153392518
|
A | G | 82 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(79): Show | 84 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.277-1744A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392518 | ||||||
chr4:153392537
|
A | G | 22 | a0001c0001t0003g0048a0001c0002t0003g0011a0001c0002t0003g0012others(19): Show | 23 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.277-1725A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392537 | ||||||
chr4:153392652
|
A | C | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-1610A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392652 | ||||||
chr4:153392706
|
A | C | 19 | a0001c0001t0003g0048a0001c0002t0003g0011a0001c0002t0003g0012others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.277-1556A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392706 | ||||||
chr4:153392731
|
A | G | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-1531A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392731 | ||||||
chr4:153392835
|
A | G | 1 | a0001c0002t0003g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.277-1427A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392835 | ||||||
chr4:153392892
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0216 | 2 | HG00140.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.277-1370G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392892 | ||||||
chr4:153392941
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.277-1321G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153392941 | ||||||
chr4:153393026
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-1236G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393026 | ||||||
chr4:153393068
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.277-1194A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393068 | ||||||
chr4:153393244
|
A | T | 1 | a0001c0001t0002g0005 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.277-1018A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393244 | ||||||
chr4:153393284
|
A | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(36): Show | 41 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.277-978A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393284 | ||||||
chr4:153393368
|
C | CT | 20 | a0001c0001t0002g0258a0001c0001t0003g0048a0001c0002t0003g0011others(17): Show | 21 | HG01071.hp2 HG01081.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.277-874dupT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153393368 | |||||
chr4:153393368
|
CT | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(56): Show | 61 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.277-874delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153393368 | |||||
chr4:153393372
|
T | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.277-890T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393372 | ||||||
chr4:153393372
|
T | TC | 3 | a0001c0001t0002g0276a0001c0001t0002g0283a0001c0001t0002g0297 | 3 | NA18941.hp2 NA19068.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.277-890_277-889ins others(1): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393372 | ||||||
chr4:153393373
|
T | C | 79 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(76): Show | 81 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.277-889T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393373 | ||||||
chr4:153393378
|
T | C | 2 | a0001c0001t0002g0306a0001c0001t0002g0307 | 2 | NA18952.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.277-884T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393378 | ||||||
chr4:153393397
|
G | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(36): Show | 41 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.277-865G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393397 | ||||||
chr4:153393427
|
A | G | 1 | a0001c0002t0001g0129 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.277-835A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393427 | ||||||
chr4:153393493
|
C | T | 2 | a0001c0002t0003g0122a0001c0002t0003g0123 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.277-769C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393493 | ||||||
chr4:153393579
|
G | A | 82 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(79): Show | 84 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.277-683G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393579 | ||||||
chr4:153393779
|
C | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(219): Show | 228 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.277-483C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393779 | ||||||
chr4:153393924
|
C | CT | 53 | a0001c0001t0001g0007a0001c0001t0001g0145a0001c0001t0001g0152others(50): Show | 53 | HG00323.hp2 HG00597.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.277-314dupT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153393924 | |||||
chr4:153393924
|
C | CTT | 22 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(19): Show | 23 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.277-315_277-314dup others(2): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153393924 | |||||
chr4:153393924
|
C | CTTT | 52 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(49): Show | 53 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.277-316_277-314dup others(3): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153393924 | |||||
chr4:153393924
|
C | CTTTT | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(55): Show | 60 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.277-317_277-314dup others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153393924 | |||||
chr4:153393924
|
C | CTTTTTT | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-319_277-314dup others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153393924 | |||||
chr4:153393924
|
CT | C | 9 | a0001c0001t0001g0137a0001c0001t0001g0169a0001c0001t0001g0194others(6): Show | 9 | HG01069.hp1 HG01515.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.277-314delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 153393924 | |||||
chr4:153393965
|
C | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-297C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393965 | ||||||
chr4:153393990
|
C | T | 9 | a0001c0001t0002g0115a0001c0001t0002g0262a0001c0001t0002g0263others(6): Show | 9 | HG00597.hp1 HG02040.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.277-272C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393990 | ||||||
chr4:153393991
|
G | A | 3 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114 | 3 | HG02109.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.277-271G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153393991 | ||||||
chr4:153394022
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0164 | 2 | HG01884.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.277-240C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153394022 | ||||||
chr4:153394047
|
G | A | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(2): Show | 5 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-215G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153394047 | ||||||
chr4:153394169
|
C | T | 2 | a0001c0001t0002g0091a0001c0001t0002g0092 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.277-93C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153394169 | ||||||
chr4:153394188
|
T | C | 82 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(79): Show | 84 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.277-74T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 4/7 | chr4 | 153394188 | ||||||
chr4:153394409
|
G | C | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.351+73G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | chr4 | 153394409 | ||||||
chr4:153394646
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.351+310G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | chr4 | 153394646 | ||||||
chr4:153394747
|
CT | C | 40 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(37): Show | 41 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.351+415delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 153394747 | |||||
chr4:153394784
|
C | T | 109 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(106): Show | 112 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.351+448C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | chr4 | 153394784 | ||||||
chr4:153395065
|
G | T | 2 | a0001c0001t0002g0306a0001c0001t0002g0307 | 2 | NA18952.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.351+729G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | chr4 | 153395065 | ||||||
chr4:153395237
|
A | G | 22 | a0001c0001t0003g0048a0001c0002t0003g0011a0001c0002t0003g0012others(19): Show | 23 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.351+901A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | chr4 | 153395237 | ||||||
chr4:153395917
|
A | G | 137 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(134): Show | 140 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.352-1302A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | chr4 | 153395917 | ||||||
chr4:153396003
|
G | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.352-1216G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | chr4 | 153396003 | ||||||
chr4:153396022
|
G | C | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(2): Show | 5 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-1197G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | chr4 | 153396022 | ||||||
chr4:153396235
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.352-984G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | chr4 | 153396235 | ||||||
chr4:153396456
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0070 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.352-763G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | chr4 | 153396456 | ||||||
chr4:153396470
|
G | C | 4 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0246others(1): Show | 4 | NA18942.hp2 NA18968.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-749G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | chr4 | 153396470 | ||||||
chr4:153396536
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.352-683G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | chr4 | 153396536 | ||||||
chr4:153396776
|
C | A | 4 | a0001c0001t0001g0192a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-443C>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | chr4 | 153396776 | ||||||
chr4:153396857
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.352-362T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | chr4 | 153396857 | ||||||
chr4:153396911
|
T | TA | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(66): Show | 72 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.352-307dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 153396911 | |||||
chr4:153397402
|
C | T | 27 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(24): Show | 28 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.466+69C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153397402 | ||||||
chr4:153397479
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.466+146A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153397479 | ||||||
chr4:153397511
|
T | C | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.466+178T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153397511 | ||||||
chr4:153397653
|
C | CA | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(78): Show | 84 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.466+330dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153397653 | |||||
chr4:153397660
|
A | AG | 23 | a0001c0001t0003g0048a0001c0001t0003g0189a0001c0002t0003g0011others(20): Show | 24 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.466+327_466+328ins others(1): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153397660 | ||||||
chr4:153397706
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.466+373G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153397706 | ||||||
chr4:153397923
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.466+590C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153397923 | ||||||
chr4:153397930
|
TATA | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 82 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.466+599_466+601del others(3): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153397930 | |||||
chr4:153397935
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.466+602G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153397935 | ||||||
chr4:153397954
|
T | C | 130 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(127): Show | 133 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.466+621T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153397954 | ||||||
chr4:153398033
|
A | T | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(2): Show | 5 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+700A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153398033 | ||||||
chr4:153398040
|
G | C | 1 | a0001c0001t0001g0224 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.466+707G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153398040 | ||||||
chr4:153398069
|
C | T | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.466+736C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153398069 | ||||||
chr4:153398317
|
A | T | 23 | a0001c0001t0003g0048a0001c0001t0003g0189a0001c0002t0003g0011others(20): Show | 24 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.466+984A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153398317 | ||||||
chr4:153398351
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.466+1018G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153398351 | ||||||
chr4:153398377
|
G | T | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.466+1044G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153398377 | ||||||
chr4:153398438
|
T | A | 1 | a0001c0001t0001g0222 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.466+1105T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153398438 | ||||||
chr4:153398477
|
T | A | 4 | a0001c0001t0002g0321a0001c0001t0002g0322a0001c0001t0002g0323others(1): Show | 4 | HG01891.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+1144T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153398477 | ||||||
chr4:153398503
|
A | T | 130 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(127): Show | 133 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.466+1170A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153398503 | ||||||
chr4:153398538
|
G | C | 1 | a0001c0001t0001g0224 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.466+1205G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153398538 | ||||||
chr4:153398719
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.466+1386A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153398719 | ||||||
chr4:153398983
|
G | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0216 | 2 | HG00140.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.466+1650G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153398983 | ||||||
chr4:153399166
|
C | T | 3 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG02280.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.466+1833C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153399166 | ||||||
chr4:153399549
|
T | C | 109 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(106): Show | 112 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.466+2216T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153399549 | ||||||
chr4:153399653
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.466+2320A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153399653 | ||||||
chr4:153399704
|
C | T | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.466+2371C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153399704 | ||||||
chr4:153399742
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.466+2409T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153399742 | ||||||
chr4:153399834
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.466+2501A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153399834 | ||||||
chr4:153399889
|
G | A | 2 | a0001c0002t0003g0130a0001c0002t0003g0131 | 2 | HG01891.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.466+2556G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153399889 | ||||||
chr4:153399890
|
AT | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(64): Show | 68 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.466+2585delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153399890 | |||||
chr4:153399890
|
ATT | A | 162 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0061others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.466+2584_466+2585d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153399890 | |||||
chr4:153399890
|
ATTT | A | 32 | a0001c0001t0001g0235a0001c0001t0002g0005a0001c0001t0002g0006others(29): Show | 34 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.466+2583_466+2585d others(5): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153399890 | |||||
chr4:153399890
|
ATTTT | A | 20 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(17): Show | 20 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.466+2582_466+2585d others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153399890 | |||||
chr4:153399890
|
ATTTTTTT others(5): Show |
A | 3 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0042 | 3 | HG01109.hp1 NA18990.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.466+2574_466+2585d others(14): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153399890 | |||||
chr4:153399890
|
ATTTTTTT others(6): Show |
A | 36 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(33): Show | 38 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.466+2573_466+2585d others(15): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153399890 | |||||
chr4:153399913
|
T | C | 1 | a0001c0001t0002g0318 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.466+2580T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153399913 | ||||||
chr4:153400238
|
G | A | 11 | a0001c0001t0001g0137a0001c0001t0001g0148a0001c0001t0001g0156others(8): Show | 11 | HG00609.hp1 HG00621.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.466+2905G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153400238 | ||||||
chr4:153400405
|
T | C | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.466+3072T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153400405 | ||||||
chr4:153400414
|
A | T | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.466+3081A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153400414 | ||||||
chr4:153400518
|
T | G | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.466+3185T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153400518 | ||||||
chr4:153400747
|
A | ATT | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(36): Show | 41 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.466+3415_466+3416d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153400747 | |||||
chr4:153400888
|
A | C | 1 | a0001c0001t0001g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.466+3555A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153400888 | ||||||
chr4:153401059
|
T | C | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.466+3726T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153401059 | ||||||
chr4:153401077
|
A | G | 12 | a0001c0001t0003g0048a0001c0002t0003g0090a0001c0002t0003g0116others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.466+3744A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153401077 | ||||||
chr4:153401140
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.466+3807C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153401140 | ||||||
chr4:153401359
|
A | T | 1 | a0001c0001t0001g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.466+4026A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153401359 | ||||||
chr4:153401525
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.466+4192T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153401525 | ||||||
chr4:153401549
|
T | TGAAATTA others(330): Show |
3 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0110 | 3 | HG02965.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.466+4232_466+4233i others(339): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153401549 | |||||
chr4:153401549
|
T | TGAAATTA others(331): Show |
3 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0109 | 3 | HG02055.hp2 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.466+4232_466+4233i others(340): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153401549 | |||||
chr4:153401549
|
T | TGAAATTA others(332): Show |
1 | a0001c0001t0001g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.466+4232_466+4233i others(341): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153401549 | |||||
chr4:153401607
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.466+4274C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153401607 | ||||||
chr4:153401615
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.466+4282C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153401615 | ||||||
chr4:153401847
|
A | G | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.466+4514A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153401847 | ||||||
chr4:153401874
|
T | C | 1 | a0001c0001t0002g0276 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.466+4541T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153401874 | ||||||
chr4:153402069
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.466+4736C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153402069 | ||||||
chr4:153402286
|
T | C | 1 | a0001c0002t0003g0131 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.466+4953T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153402286 | ||||||
chr4:153402450
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.466+5117G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153402450 | ||||||
chr4:153402579
|
G | T | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.466+5246G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153402579 | ||||||
chr4:153402876
|
G | A | 106 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(103): Show | 108 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.466+5543G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153402876 | ||||||
chr4:153402905
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.466+5572C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153402905 | ||||||
chr4:153402997
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.466+5664A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153402997 | ||||||
chr4:153403055
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.466+5722G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153403055 | ||||||
chr4:153403133
|
T | A | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.466+5800T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153403133 | ||||||
chr4:153403239
|
C | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.467-5732C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153403239 | ||||||
chr4:153403304
|
A | G | 106 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(103): Show | 108 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.467-5667A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153403304 | ||||||
chr4:153403343
|
G | A | 23 | a0001c0001t0003g0048a0001c0001t0003g0189a0001c0002t0003g0011others(20): Show | 24 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.467-5628G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153403343 | ||||||
chr4:153403355
|
A | G | 16 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(13): Show | 16 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.467-5616A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153403355 | ||||||
chr4:153403510
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.467-5461A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153403510 | ||||||
chr4:153403775
|
C | CT | 24 | a0001c0001t0001g0151a0001c0001t0003g0048a0001c0001t0003g0189others(21): Show | 25 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.467-5186dupT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153403775 | |||||
chr4:153404015
|
A | G | 14 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(11): Show | 15 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.467-4956A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404015 | ||||||
chr4:153404039
|
T | TCA | 14 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(11): Show | 15 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.467-4926_467-4925d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153404039 | |||||
chr4:153404053
|
G | A | 130 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(127): Show | 133 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.467-4918G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404053 | ||||||
chr4:153404080
|
G | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0180a0001c0001t0001g0233 | 3 | NA18939.hp1 NA18955.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.467-4891G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404080 | ||||||
chr4:153404170
|
G | T | 1 | a0001c0001t0002g0256 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.467-4801G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404170 | ||||||
chr4:153404174
|
C | CT | 48 | a0001c0001t0001g0033a0001c0001t0001g0105a0001c0001t0001g0107others(45): Show | 48 | HG00597.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.467-4771dupT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153404174 | |||||
chr4:153404174
|
CT | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(77): Show | 83 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.467-4771delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153404174 | |||||
chr4:153404174
|
CTT | C | 30 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0072others(27): Show | 30 | HG01255.hp2 HG01256.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.467-4772_467-4771d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153404174 | |||||
chr4:153404328
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.467-4643C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404328 | ||||||
chr4:153404330
|
T | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.467-4641T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404330 | ||||||
chr4:153404345
|
CT | C | 111 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(108): Show | 113 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.467-4609delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153404345 | |||||
chr4:153404345
|
CTT | C | 17 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(14): Show | 17 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.467-4610_467-4609d others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153404345 | |||||
chr4:153404367
|
A | G | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.467-4604A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404367 | ||||||
chr4:153404485
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.467-4486C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404485 | ||||||
chr4:153404561
|
G | A | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(2): Show | 5 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-4410G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404561 | ||||||
chr4:153404652
|
C | T | 137 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(134): Show | 140 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.467-4319C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404652 | ||||||
chr4:153404675
|
C | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.467-4296C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404675 | ||||||
chr4:153404731
|
G | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(11): Show | 15 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.467-4240G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404731 | ||||||
chr4:153404788
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.467-4183G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404788 | ||||||
chr4:153404798
|
C | T | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.467-4173C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404798 | ||||||
chr4:153404923
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.467-4048C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404923 | ||||||
chr4:153404924
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0217 | 2 | HG02056.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.467-4047G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153404924 | ||||||
chr4:153405541
|
GA | G | 188 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(185): Show | 192 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.467-3418delA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153405541 | |||||
chr4:153405622
|
G | T | 1 | a0001c0002t0003g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.467-3349G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153405622 | ||||||
chr4:153405667
|
A | C | 2 | a0001c0002t0003g0127a0001c0002t0003g0128 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.467-3304A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153405667 | ||||||
chr4:153405700
|
A | G | 3 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG02280.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.467-3271A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153405700 | ||||||
chr4:153405708
|
A | C | 1 | a0001c0001t0001g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.467-3263A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153405708 | ||||||
chr4:153405804
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0066 | 2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.467-3167A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153405804 | ||||||
chr4:153405836
|
A | G | 130 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(127): Show | 133 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.467-3135A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153405836 | ||||||
chr4:153405884
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.467-3087A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153405884 | ||||||
chr4:153405960
|
C | T | 3 | a0001c0003t0004g0004a0001c0003t0004g0099a0001c0003t0004g0100 | 4 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-3011C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153405960 | ||||||
chr4:153405993
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.467-2978G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153405993 | ||||||
chr4:153405996
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.467-2975A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153405996 | ||||||
chr4:153406046
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.467-2925C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153406046 | ||||||
chr4:153406047
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.467-2924G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153406047 | ||||||
chr4:153406080
|
G | A | 2 | a0001c0001t0002g0334a0001c0001t0002g0335 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.467-2891G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153406080 | ||||||
chr4:153406099
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.467-2872C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153406099 | ||||||
chr4:153406436
|
C | T | 8 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(5): Show | 8 | HG00323.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.467-2535C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153406436 | ||||||
chr4:153406437
|
G | A | 9 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(6): Show | 9 | HG02257.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.467-2534G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153406437 | ||||||
chr4:153406667
|
T | C | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.467-2304T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153406667 | ||||||
chr4:153406872
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.467-2099C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153406872 | ||||||
chr4:153406916
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.467-2055C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153406916 | ||||||
chr4:153406949
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.467-2022G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153406949 | ||||||
chr4:153407029
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.467-1942C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153407029 | ||||||
chr4:153407038
|
A | T | 1 | a0001c0002t0003g0131 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.467-1933A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153407038 | ||||||
chr4:153407239
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.467-1732G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153407239 | ||||||
chr4:153407440
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.467-1531G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153407440 | ||||||
chr4:153407783
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.467-1188G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153407783 | ||||||
chr4:153407836
|
C | T | 3 | a0001c0003t0004g0004a0001c0003t0004g0099a0001c0003t0004g0100 | 4 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-1135C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153407836 | ||||||
chr4:153407976
|
A | C | 1 | a0001c0001t0001g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.467-995A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153407976 | ||||||
chr4:153407979
|
A | C | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.467-992A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153407979 | ||||||
chr4:153407990
|
T | C | 101 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(98): Show | 103 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.467-981T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153407990 | ||||||
chr4:153408175
|
C | T | 1 | a0001c0002t0003g0119 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.467-796C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153408175 | ||||||
chr4:153408214
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.467-757G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153408214 | ||||||
chr4:153408219
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.467-752A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153408219 | ||||||
chr4:153408407
|
T | C | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.467-564T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153408407 | ||||||
chr4:153408477
|
T | TTAACTC | 45 | a0001c0001t0002g0265a0001c0001t0002g0267a0001c0001t0002g0271others(42): Show | 46 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.467-491_467-490ins others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153408477 | |||||
chr4:153408653
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.467-318A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153408653 | ||||||
chr4:153408690
|
G | A | 23 | a0001c0001t0003g0048a0001c0001t0003g0189a0001c0002t0003g0011others(20): Show | 24 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.467-281G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153408690 | ||||||
chr4:153408752
|
C | T | 1 | a0001c0001t0002g0250 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.467-219C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153408752 | ||||||
chr4:153408912
|
G | GTA | 20 | a0001c0001t0001g0174a0001c0001t0002g0044a0001c0001t0002g0045others(17): Show | 20 | HG01256.hp1 HG03017.hp1 HG03195.hp1 others(17): Show |
intron_variant | MODIFIER | c.467-38_467-37dupTA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153408912 | |||||
chr4:153408912
|
G | GTATA | 3 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG02280.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.467-40_467-37dupTA others(2): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153408912 | |||||
chr4:153408912
|
G | GTATATA | 60 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(57): Show | 62 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.467-42_467-37dupTA others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153408912 | |||||
chr4:153408912
|
G | GTATATAT others(1): Show |
16 | a0001c0001t0002g0115a0001c0001t0002g0265a0001c0001t0002g0280others(13): Show | 16 | HG00408.hp2 HG02055.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.467-44_467-37dupTA others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153408912 | |||||
chr4:153408912
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0002g0330 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.467-46_467-37dupTA others(8): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153408912 | |||||
chr4:153408912
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0002g0315 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.467-48_467-37dupTA others(10): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153408912 | |||||
chr4:153408912
|
G | GTGTA | 15 | a0001c0002t0003g0090a0001c0002t0003g0116a0001c0002t0003g0117others(12): Show | 16 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.467-58_467-57insGT others(2): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153408912 | |||||
chr4:153408912
|
G | GTGTATA | 6 | a0001c0001t0003g0048a0001c0001t0003g0189a0001c0002t0003g0011others(3): Show | 6 | HG01243.hp1 HG01891.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-58_467-57insGT others(4): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153408912 | |||||
chr4:153408912
|
G | GTGTATAT others(1): Show |
4 | a0001c0001t0002g0275a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | NA18984.hp1 NA18992.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-58_467-57insGT others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153408912 | |||||
chr4:153408912
|
GTA | G | 37 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(34): Show | 37 | HG01255.hp2 HG02109.hp1 HG02145.hp2 others(34): Show |
intron_variant | MODIFIER | c.467-38_467-37delTA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153408912 | |||||
chr4:153408914
|
A | ATATATAT others(25): Show |
52 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(49): Show | 55 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.467-39_467-38insAA others(30): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153408914 | |||||
chr4:153408914
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0074 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.467-46_467-13dupTA others(32): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 153408914 | |||||
chr4:153408914
|
A | G | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.467-57A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153408914 | ||||||
chr4:153408933
|
T | A | 19 | a0001c0001t0003g0048a0001c0002t0003g0011a0001c0002t0003g0012others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.467-38T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 6/7 | chr4 | 153408933 | ||||||
chr4:153409019
|
T | C | 4 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG02965.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.511+4T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153409019 | ||||||
chr4:153409154
|
A | G | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.511+139A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153409154 | ||||||
chr4:153409279
|
A | G | 6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.511+264A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153409279 | ||||||
chr4:153409370
|
C | CTAATAA | 33 | a0001c0001t0002g0265a0001c0001t0002g0267a0001c0001t0002g0271others(30): Show | 34 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.511+370_511+375dup others(6): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153409370 | |||||
chr4:153409370
|
C | CTAATAAT others(2): Show |
97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(94): Show | 100 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.511+367_511+375dup others(9): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153409370 | |||||
chr4:153409370
|
C | CTAATAAT others(5): Show |
1 | a0001c0001t0001g0085 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.511+364_511+375dup others(12): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153409370 | |||||
chr4:153409370
|
C | CTAATAAT others(8): Show |
13 | a0001c0001t0002g0014a0001c0001t0002g0295a0001c0001t0002g0326others(10): Show | 13 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.511+361_511+375dup others(15): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153409370 | |||||
chr4:153409370
|
C | CTAATAAT others(11): Show |
31 | a0001c0001t0002g0082a0001c0001t0002g0087a0001c0001t0002g0112others(28): Show | 31 | HG00408.hp2 HG00597.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.511+358_511+375dup others(18): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153409370 | |||||
chr4:153409370
|
C | CTAATAAT others(14): Show |
40 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0044others(37): Show | 42 | HG00323.hp1 HG00741.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.511+375_511+376ins others(21): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153409370 | |||||
chr4:153409515
|
C | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.511+500C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153409515 | ||||||
chr4:153409614
|
C | T | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0259others(2): Show | 5 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.511+599C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153409614 | ||||||
chr4:153409637
|
T | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.511+622T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153409637 | ||||||
chr4:153409649
|
G | A | 1 | a0001c0001t0002g0320 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.511+634G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153409649 | ||||||
chr4:153409762
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.511+747G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153409762 | ||||||
chr4:153409764
|
ATT | A | 23 | a0001c0001t0003g0048a0001c0001t0003g0189a0001c0002t0003g0011others(20): Show | 24 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.511+758_511+759del others(2): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153409764 | |||||
chr4:153409948
|
G | A | 2 | a0001c0001t0002g0284a0001c0001t0002g0320 | 2 | HG01496.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.511+933G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153409948 | ||||||
chr4:153410038
|
A | G | 129 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(126): Show | 132 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.511+1023A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153410038 | ||||||
chr4:153410284
|
C | CT | 7 | a0001c0001t0001g0138a0001c0001t0002g0091a0001c0001t0002g0092others(4): Show | 7 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.511+1280dupT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153410284 | |||||
chr4:153410284
|
CT | C | 24 | a0001c0001t0001g0105a0001c0001t0003g0048a0001c0001t0003g0189others(21): Show | 25 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.511+1280delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153410284 | |||||
chr4:153410571
|
A | C | 23 | a0001c0001t0003g0048a0001c0001t0003g0189a0001c0002t0003g0011others(20): Show | 24 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.511+1556A>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153410571 | ||||||
chr4:153410729
|
G | T | 1 | a0001c0001t0001g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.511+1714G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153410729 | ||||||
chr4:153410943
|
A | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(36): Show | 41 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.511+1928A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153410943 | ||||||
chr4:153410984
|
G | C | 1 | a0001c0001t0001g0163 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.511+1969G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153410984 | ||||||
chr4:153411061
|
G | A | 23 | a0001c0001t0003g0048a0001c0001t0003g0189a0001c0002t0003g0011others(20): Show | 24 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.511+2046G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153411061 | ||||||
chr4:153411084
|
A | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0170 | 2 | NA18981.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.511+2069A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153411084 | ||||||
chr4:153411850
|
T | G | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.511+2835T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153411850 | ||||||
chr4:153411880
|
T | G | 1 | a0001c0001t0001g0165 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.511+2865T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153411880 | ||||||
chr4:153411946
|
T | C | 4 | a0001c0001t0002g0322a0001c0003t0004g0004a0001c0003t0004g0099others(1): Show | 5 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.512-2805T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153411946 | ||||||
chr4:153412484
|
C | CT | 26 | a0001c0001t0001g0036a0001c0001t0001g0101a0001c0001t0001g0102others(23): Show | 26 | HG01256.hp1 HG02027.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.512-2251dupT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153412484 | |||||
chr4:153412484
|
CT | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(41): Show | 45 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.512-2251delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153412484 | |||||
chr4:153412510
|
T | A | 1 | a0001c0001t0001g0219 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.512-2241T>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153412510 | ||||||
chr4:153412544
|
G | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(11): Show | 15 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.512-2207G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153412544 | ||||||
chr4:153412578
|
G | A | 3 | a0001c0003t0004g0004a0001c0003t0004g0099a0001c0003t0004g0100 | 4 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-2173G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153412578 | ||||||
chr4:153412605
|
T | C | 130 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(127): Show | 133 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.512-2146T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153412605 | ||||||
chr4:153412726
|
A | G | 1 | a0001c0002t0003g0120 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.512-2025A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153412726 | ||||||
chr4:153412739
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.512-2012C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153412739 | ||||||
chr4:153412794
|
TTTC | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.512-1951_512-1949d others(5): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153412794 | |||||
chr4:153412800
|
C | CT | 10 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(7): Show | 10 | HG01255.hp2 HG02109.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.512-1943dupT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153412800 | |||||
chr4:153412809
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.512-1942C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153412809 | ||||||
chr4:153412809
|
CT | C | 26 | a0001c0001t0001g0047a0001c0001t0001g0197a0001c0001t0002g0255others(23): Show | 27 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.512-1928delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153412809 | |||||
chr4:153412863
|
G | C | 23 | a0001c0001t0003g0048a0001c0001t0003g0189a0001c0002t0003g0011others(20): Show | 24 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.512-1888G>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153412863 | ||||||
chr4:153412943
|
T | TA | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.512-1807dupA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153412943 | |||||
chr4:153413011
|
C | G | 1 | a0001c0001t0002g0312 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.512-1740C>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413011 | ||||||
chr4:153413011
|
C | T | 106 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(103): Show | 108 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.512-1740C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413011 | ||||||
chr4:153413012
|
G | A | 23 | a0001c0001t0003g0048a0001c0001t0003g0189a0001c0002t0003g0011others(20): Show | 24 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.512-1739G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413012 | ||||||
chr4:153413042
|
T | C | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.512-1709T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413042 | ||||||
chr4:153413062
|
T | C | 23 | a0001c0001t0003g0048a0001c0001t0003g0189a0001c0002t0003g0011others(20): Show | 24 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.512-1689T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413062 | ||||||
chr4:153413092
|
A | G | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.512-1659A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413092 | ||||||
chr4:153413142
|
G | T | 8 | a0001c0001t0002g0262a0001c0001t0002g0263a0001c0001t0002g0264others(5): Show | 8 | HG00597.hp1 HG02040.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.512-1609G>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413142 | ||||||
chr4:153413144
|
C | T | 8 | a0001c0001t0002g0262a0001c0001t0002g0263a0001c0001t0002g0264others(5): Show | 8 | HG00597.hp1 HG02040.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.512-1607C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413144 | ||||||
chr4:153413179
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0110 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.512-1572T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413179 | ||||||
chr4:153413258
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.512-1493A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413258 | ||||||
chr4:153413292
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.512-1459C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413292 | ||||||
chr4:153413366
|
A | G | 3 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG02280.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.512-1385A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413366 | ||||||
chr4:153413416
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0216 | 2 | HG00140.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.512-1335A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413416 | ||||||
chr4:153413460
|
T | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.512-1291T>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413460 | ||||||
chr4:153413566
|
C | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.512-1185C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413566 | ||||||
chr4:153413633
|
A | G | 130 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(127): Show | 133 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.512-1118A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413633 | ||||||
chr4:153413634
|
T | C | 130 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(127): Show | 133 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.512-1117T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413634 | ||||||
chr4:153413687
|
GA | G | 86 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(83): Show | 88 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.512-1051delA | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153413687 | |||||
chr4:153413700
|
A | G | 1 | a0002c0004t0002g0292 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.512-1051A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413700 | ||||||
chr4:153413702
|
G | A | 1 | a0002c0004t0002g0292 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.512-1049G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413702 | ||||||
chr4:153413744
|
A | G | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.512-1007A>G | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413744 | ||||||
chr4:153413761
|
A | T | 1 | a0001c0001t0002g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.512-990A>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153413761 | ||||||
chr4:153414119
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.512-632T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153414119 | ||||||
chr4:153414285
|
C | CT | 19 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0241others(16): Show | 19 | HG01256.hp1 HG03017.hp1 HG03654.hp2 others(16): Show |
intron_variant | MODIFIER | c.512-453dupT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153414285 | |||||
chr4:153414285
|
CT | C | 25 | a0001c0001t0001g0149a0001c0001t0002g0258a0001c0001t0003g0048others(22): Show | 26 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.512-453delT | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153414285 | |||||
chr4:153414285
|
CTT | C | 87 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(84): Show | 89 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.512-454_512-453del others(2): Show |
MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 153414285 | |||||
chr4:153414307
|
G | A | 87 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(84): Show | 89 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.512-444G>A | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153414307 | ||||||
chr4:153414384
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.512-367C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153414384 | ||||||
chr4:153414534
|
C | T | 87 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0014others(84): Show | 89 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.512-217C>T | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153414534 | ||||||
chr4:153414608
|
T | C | 1 | a0001c0002t0003g0121 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.512-143T>C | MND1 | ENSG00000121211.8 | transcript | ENST00000240488.8 | protein_coding | 7/7 | chr4 | 153414608 |